- Open Access
Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristics
Molecular Brain volume 9, Article number: 64 (2016)
Amyloid precursor protein knockout mice (APP-KO) have impaired differentiation of amacrine and horizontal cells. APP is part of a gene family and its paralogue amyloid precursor-like protein 2 (APLP2) has both shared as well as distinct expression patterns to APP, including in the retina. Given the impact of APP in the retina we investigated how APLP2 expression affected the retina using APLP2 knockout mice (APLP2-KO).
Using histology, morphometric analysis with noninvasive imaging technique and electron microscopy, we showed that APLP2-KO retina displayed abnormal formation of the outer synaptic layer, accompanied with greatly impaired photoreceptor ribbon synapses in adults. Moreover, APLP2-KO displayed a significant decease in ON-bipolar, rod bipolar and type 2 OFF-cone bipolar cells (36, 21 and 63 %, respectively). Reduction of the number of bipolar cells was accompanied with disrupted dendrites, reduced expression of metabotropic glutamate receptor 6 at the dendritic tips and alteration of axon terminals in the OFF laminae of the inner plexiform layer. In contrast, the APP-KO photoreceptor ribbon synapses and bipolar cells were intact. The APLP2-KO retina displayed numerous phenotypic similarities with the congenital stationary night blindness, a non-progressive retinal degeneration disease characterized by the loss of night vision. The pathological phenotypes in the APLP2-KO mouse correlated to altered transcription of genes involved in pre- and postsynatic structure/function, including CACNA1F, GRM6, TRMP1 and Gα0, and a normal scotopic a-wave electroretinogram amplitude, markedly reduced scotopic electroretinogram b-wave and modestly reduced photopic cone response. This confirmed the impaired function of the photoreceptor ribbon synapses and retinal bipolar cells, as is also observed in congenital stationary night blindness. Since congenital stationary night blindness present at birth, we extended our analysis to retinal differentiation and showed impaired differentiation of different bipolar cell subtypes and an altered temporal sequence of development from OFF to ON laminae in the inner plexiform layer. This was associated with the altered expression patterns of bipolar cell generation and differentiation factors, including MATH3, CHX10, VSX1 and OTX2.
These findings demonstrate that APLP2 couples retina development and synaptic genes and present the first evidence that APLP2 expression may be linked to synaptic disease.
The amyloid precursor protein (APP) is known to play, together with its proteolytic fragments, numerous and varied roles in cell physiology and pathology, including in Alzheimer disease [1–4]. The amyloid precursor-like protein 2 (APLP2) belongs to the APP gene family. Phylogenetic analysis suggests the functions of APP, APLP1 and APLP2 have diverged after duplication to mediate distinct neuronal actions . Our knowledge of the physiological and pathophysiological functions of APLP2 remains poor relative to APP functions, and no neuronal pathology has been definitively associated with APLP2. In contrast, APLP2 has recently been identified as one of the myopia genes and APLP2-KO mice develop high degrees of hyperopia . APLP2 expression patterns during brain development suggest an important role in maturation of specific neuronal subtypes in the central nervous system (CNS) [7–9]. However, the expression or role of APLP2 in the developing and adult retina, and whether there is functional redundancy between APLP2 and APP in the retina, is not known.
As part of the CNS, the neural retina is arranged in well-defined laminar structures. Photoreceptors (rods and cones) transmit visual information to ganglion cells via bipolar cells. In the “classical” rod pathway, rods feed into rod bipolar cells that provide input to both the ON and OFF pathway via AII/glycinergic amacrine cells. The rod bipolar cell light-evoked response is initiated by a decrease in glutamate occupancy of mGluR6, which decreases its G-protein activity culminating in the opening of the TRPM1 channel [10–12]. The mGluR6-mediated modulation of TRPM1 also is known to require several other proteins including Gαo and GRP179 [12–16] and other known components with unresolved function including Nyctalopin and LRIT3 . Most of these proteins are localized at the dendritic tips of ON-bipolar cells. In adult mice, APP is expressed in horizontal, bipolar, amacrine and ganglion cells and on the two retinal synaptic layers: inner plexiform layer (IPL) and outer plexiform layer (OPL) [18, 19]. The IPL contains bipolar-ganglion cell connections and modulatory amacrine conventional synapses. We showed that APP is necessary for the differentiation of AII amacrine cells . The OPL contains the ribbon synapses between photoreceptor cells and the bipolar and horizontal interneurons. Defects at these synapses led to congenital stationary night blindness (CSNB).
CSNB encompasses a group of genetically and clinically heterogeneous retinal disorders that primarily affect night vision. The non-progressive night vision loss is present at birth and there is no cure for CSNB. The prevalence of CSNB is approximately 1 in 10,000 . CSNB is caused by mutations in seventeen identified genes with an unknown number yet to be identified and inherited in an autosomal dominant, autosomal recessive or X-linked recessive manner [21–23]. Clinically, CSNB is classified as the Riggs type and the Schubert-Bornschein type based on specific waveforms on the electroretinogram (ERG). The rare Riggs type is characterized by decreased scotopic a-wave amplitude in keeping with rod photoreceptor dysfunction and by normal cone system . This should be distinguished from the Schubert-Bornschein type of ERG abnormalities in which scotopic a-wave amplitude is normal . The Schubert-Bornschein type is divided into two sub-types, complete CSNB (cCSNB or CSNB1), associated with a drastically reduced or completely abolished scotopic b-wave response, because of a failure to transmit the photoreceptor signal through the ON bipolar cells, and incomplete CSNB (iCSNB or CSNB2), which is associated with a reduced scotopic b-wave and reduced photopic cone responses indicating ON- and OFF-bipolar cell dysfunction . cCNSB has been associated with mutations in genes that encode postsynaptic proteins which are required for the signal transduction cascade responsible for bipolar cell depolarization, including GRM6, TRPM1, GRP179, NYX and LRIT3 [27–33]. Mutations in CACNA1F were identified in patients with iCNSB [34, 35]. CACNA1F encodes the α1F subunit of the L-type voltage-gated Ca2+ channel, Cav1.4, and is located at the photoreceptor ribbon synapse. Abnormal synapses in the outer nuclear layer (ONL) detected by a noninvasive imaging technique using optical coherence tomography (OCT) have been observed in some cases of iCSNB , while thinning of the ganglion cell layer (GCL), IPL and inner nuclear layer (INL) in other iCSNB cases . Mutations in CABP4, encoding a Ca2+-binding protein located in photoreceptor synaptic terminals and associated with Cav1.4, lead to autosomal recessive iCSNB . Most of the cases associated with CABP4 mutations have recently been shown to display high hyperopia [39, 40]. A minority of iCSNB patients have impaired night vision compared to cCSNB  and they have less severely impaired night vision and have a more variable phenotype with respect to the visual acuity, refractive error (myopia/hyperopia) and the b/a wave amplitude ratios of the scotopic ERG than those with cCSNB . In mouse models of iCSNB, both hypo- and hyperactivated channels accomplished respectively by deletion of CABP4 and the Cacna1f I745T mutation lead to similar ERG alterations, visual impairments and an improper maturation of the synapse architecture [42, 43], indicating that impaired retinal synaptogenesis may contribute to vision impairment in iCSNB.
Although different genes responsible for the pathogenic mechanisms of CSNB have been identified, further studies are needed to clarify the molecular mechanisms of the disease. For CSNB patients in whom the genetic causes are still to be discovered, mutations are likely to be found in genes that function in photoreceptor pre- and postsynaptic processes that affect retinal transmission. It was suggested that BHLHB4, MATH5, or PRDM8, which encode three transcription factors required for either maturation of rod bipolar cells or differentiation of several bipolar cell subtypes, may be candidate genes for CSNB [44, 45]. Recently, the differentiation factor of rod bipolar cells, PRDM8, was presented as a candidate gene for CSNB , reinforcing the importance to study the mechanisms of bipolar cell differentiation for elucidating the pathological events involved in CSNB. A canine pedigree of cCSNB where the ON-bipolar cell function is compromised has been recently characterized . In this study all known CSNB genes have been excluded, suggesting the existence of still to be identified genes involved in the disease process.
Given the role of APLP2 in synapse function in adult brain and peripheral nervous system (PNS) [3, 48], and the effect of APP on the differentiation of AII amacrine cells , we investigated the role of APLP2 in synaptic lamination in the adult retina using APLP2-KO mice. APLP2-KO mice display no signs of retinal degeneration in young and adult. In this study, the lack of APLP2 expression resulted in numerous phenotypic similarities to CSNB. APLP2-KO retina had a nonprogressive reduction of the scotopic ERG b-wave and the photopic cone responses. This was associated with an affected OPL structure comprising impaired presynaptic photoreceptor ribbon complex and a postsynaptic element of ON and OFF-bipolar cells resembling iCSNB. We describe for the first time the role of APLP2 in neuronal differentiation which involves regulating the temporal expression of a combination of intrinsic factors implicated in the control of bipolar cell generation (early postnatal) and differentiation (late postnatal) during development, and in pre and postsynatic structure/function in adults. APLP2 may be a link between retina development and synaptic genes involved in the pathogenic events in CSNB.
Laminar expression of APLP2 in postnatal developing and adult retinas
Developmental expression of APLP2 was examined by immunohistochemistry on WT neural retinas. During postnatal development, retinal ganglion cells (RGCs) and amacrine cells are the first cells to differentiate and form the IPL (Fig. 1a). Then, horizontal cells and photoreceptors differentiate and contact each other in the outer retina, forming the OPL. Later, the vertical networks are interconnected when bipolar cells are generated and connections with ganglion cells are established. At postnatal day (PN) 1, strong APLP2 immunostaining was detected in the ganglion cell layer (GCL), which harbours RGCs, whereas weaker but uniform APLP2 immunostaining was observed in the neuroblastic layer (NBL) (Fig. 1b). At PN5, the APLP2 immunostaining remained strong in the GCL and INL, where differentiating amacrine and bipolar cells are located (Fig. 1c). At PN10, the GCL, INL and OPL, which contains the presynaptic ribbon complex of the photoreceptors and the postsynaptic plexus of the bipolar cells, were all intensely stained (Fig. 1d). However, in the IPL, which is composed of conventional synapses between RGCs and amacrine and bipolar cells, APLP2 immunostaining was heterogeneous. In adult retina, the GCL, IPL, INL and OPL immunostaining for APLP2 remained strong, whereas APLP2 immunostaining was weak in the photoreceptor layer (Fig. 1e, left panel). Control experiments with the anri-APLP2 antibody on retinal sections of APLP2-KO showed no APLP2 immunostaining (Fig. 1e, right panel). RT-PCR analysis showed that APLP2 mRNA levels from whole retina increased during the retinal differentiation period from PN1 to PN15, then plateauing at adult age (Fig. 1f).
Using a panel of antibodies against specific markers of retinal cell subtypes, we showed that APLP2 colocalized with RGCs, amacrine (starburst and AII), rod bipolar and horizontal cells in adult retina (Additional file 1: Figure S1A-F). In the IPL, APLP2 colocalized with the three calretinin-labeled laminae including the upper and lower laminae which correspond to the OFF and ON starburst cell plexuses respectively (Additional file 1: Figure S1C) and with the two strata S2 and S4 bands of the cholinergic synapses (Additional file 1: Figure S1D). In the OPL, APLP2 colocalized with VGLUT1, the only vesicular glutamate transporter located in the ribbon synapses of photoreceptors (Additional file 1: Figure S1F) and with PSD95, located presynaptically at photoreceptor synapses (cone pedicles and rod spherules) (Additional file 1: Figure S1G). Moreover, co-immunostaining with anti-APLP2 and anti-APP antibodies showed that APLP2 colocalized with APP in all synaptic and nuclear layers of neural retina (Additional file 1: Figure S1I-M).
Deletion of APLP2 alters the structure of the OPL
We investigated retinal structure in APLP2-KO by spectral domain optical coherence tomography (SD-OCT), histology and transmission electron microscopy (TEM) in young and adult mice. The SD-OCT images showed an identical laminar organization in the inner and outer retina in young APLP2-KO and WT (Fig. 2a) mice since the thicknesses of the total neural retina, inner retina (inclusive of GCL, IPL and INL) and outer retina (inclusive of OPL, ONL, OLM/IS/OS) were not significantly different (Additional file 1: Table S2). Semithin histological sections confirmed that the gross laminar structure of the retina was similar between the two genotypes (Fig. 2b). In contrast, the profile of the OPL was irregular in APLP2-KO as compared to its uniform thickness in WT (Fig. 2b, arrows). CNSB and X-linked retinoschisis (XRLS) are two main retinal disorders specifically affecting the OPL. Both disorders show altered ERG b-wave, but XLRS is progressive [49–51], while CSNB is stationary. Moreover, XLRS is characterized by a cystic degeneration of the retina, leading to a split of retinal layers and frequently accompanied with retinal pigment epithelium (RPE) atrophy and retinal detachment during adulthood. SD-OCT images (Fig. 2a) showed that overall, retinal morphology did not change over time. No focal lesions from the retinal pigment epithelium (RPE)/Bruch’s membrane complex to the GCL/NFL were observed in adult mice. No retinal detachments were observed (Fig. 2b). At high magnification (6200-8700x magnification), TEM of the RPE, in association with the photoreceptor outer segments, showed normally developed RPE with elongated apical processes into the interphotoreceptor space for WT and APLP2-KO (Additional file 1: Figure S2 A-D). The presence of phagosomes, newly engulfed by the RPE, is predicted to be the product of functional light-induced phagocytosis of the distal tip of the photoreceptor outer segment by the RPE cells. The TEM micrographs of longitudinal sections confirmed the absence of RPE atrophy and retinal detachment in adult APLP2-KO. RPE flatmounts visualized by phalloidin staining showed a uniform hexagonal array of the F-actin cytoskeletal network in WT and APLP2-KO (Additional file 1: Figure S2 E and F). Taken together, these data show a well-structured RPE/choroid complex in APLP2-KO mice.
The thicknesses of the total neural retina, inner retina and outer retina were not significantly different between young and adult APLP2-KO (Additional file 1: Table S2). The gross laminar structure of the retina was similar between the two genotypes at all ages examined (Fig. 2b). Morphometric analysis of semithin histological sections showed a comparable thickness of the neural retina in both groups of age of APLP2-KO (Fig. 2c) confirming SD-OCT data, while the photoreceptor cell nuclei number was similar between the two genotypes in both groups of age (Additional file 1: Table S2). We saw no differences between WT and APLP2-KO retinas when comparing the number of cones stained for cone arrestin (Additional file 1: Table S2). The average OPL thicknesses were not different between WT and APLP2-KO, although width of OPL was irregular in APLP2-KO (Fig. 2b arrows and c). High-magnification (1650 x magnification) TEM micrographs of longitudinal sections confirmed the irregular width in the OPL of the APLP2-KO compared to WT for both groups of age (Fig. 2d). Taken together, these data indicate that loss of APLP2 leads to a discrete stationary structural alteration of the OPL thickness.
Impaired photoreceptor-bipolar cell synaptic transmission in APLP2-KO
Due to the similarities between APLP2-KO mice and CSNB in the phenotypic features of the OPL, we hypothesized APLP2-KO mice have dysfunction in the transmission pathway from photoreceptors to bipolar cells. Therefore, we tested our hypothesis by assessing retinal function under scotopic conditions, using ERG in APLP2-KO. Figure 3a shows a series of representative ERGs of young WT and APLP2-KO mice recorded under dark-adapted conditions to flash stimuli that cover a 4-log-unit range of intensity. The scotopic ERG of WT mice shows a typical a- and b-wave pattern. At all intensities, the ERG included a positive-polarity b-wave, which represent the summed activity of rod bipolar cells, while at the higher intensities, the ERG also included a negative a-wave that is generated by the light-induced closure of cGMP-gated ion channels along the rod photoreceptor outer segments. Under a dim light (low flash intensity: −3.5 log cdsm−2), a b-wave with a subnormal amplitude was observed in young APLP2-KO (Fig. 3a and Additional file 1: Figure S3A). Under intermediate and bright flash intensities, the b-wave was markedly reduced in amplitude in APLP2-KO compared to WT. At the higher intensities, the a-wave of young APLP2-KO appeared normal. Superimposing the ERGs recorded at a flash intensity of −1.9 log cdsm−2 and 0.46 log cdsm−2 evoking a rod response and a combined rod-cone response, respectively, highlighted the difference in b-wave amplitude in young APLP2-KO and WT (Fig. 3c). The average data at all flash intensities show that the ERG a-wave was similar in young APLP2-KO and WT in amplitude (Additional file 1: Figure S3A) and implicit time (Additional file 1: Figure S3C). In contrast, the ERG b-wave amplitude was reduced in young APLP2-KO (Additional file 1: Figure S3A). However, the b-wave implicit time was not altered in APLP2-KO compared to WT (Additional file 1: Figure S3C). The maximal b-wave amplitude was significantly (p < 0.05) reduced in APLP2-KO (866 ± 191 μV) compared to WT (1218 ± 115 μV) with no alteration in half saturation luminance (K) or the slope of the b-wave sensitivity curve (n) (Additional file 1: Figure S3E). When b-wave amplitudes were normalized by calculating the b/a-wave ratio, we observed that values from young APLP2-KO were significantly lower at the brightest flash intensity (b/a: 2.9 vs. 1.9 in WT vs. APLP2-KO, respectively). These data indicate the lack of APLP2 affects the amplification gain of synaptic transmission from the photoreceptors to the bipolar cells, whereas the phototransduction in rod photoreceptors is not affected. To establish whether ERG deficits of APLP2-KO were stationary or progressive, we repeated the scotopic ERGs in adults. Figure 3b shows a series of representative ERGs of adult WT and APLP2-KO mice. Superimposing the ERGs recorded at a flash intensity of −1.9 log cdsm−2 and 0.46 log cdsm−2 highlighted the difference in b-wave amplitude in adult APLP2-KO and WT (Fig. 3c). The average data show that the ERG-a wave of adult APLP2-KO was comparable with WT (Additional file 1: Figure S3B and D), indicating that photoreceptor functions remained normal in APLP2-KO overtime. Therefore, we excluded APLP2-KO as a model of the Riggs type. ERG b-wave responses of APLP2-KO declined in amplitude at the same rate in adult and young compared to WT of the same age (compare Additional file 1: Figure S3A with Additional file 1: Figure S3B), with no alteration in the K and n parameters (Fig. 3e). In adults, the maximal b-wave amplitude was significantly (p < 0.05) reduced in APLP2-KO (772 ± 155 μV) compared to WT (1135 ± 211 μV) (Additional file 1: Figure S3E). At the brightest flash intensity, the b/a-wave ratio was significantly reduced in adult APLP2-KO compared to adult WT (b/a: 2.5 vs. 1.9 in WT vs. APLP2-KO, respectively), while similar in young and adult APLP2-KO. Therefore, we hypothesized that APLP2-KO resemble the incomplete form of the Schubert-Bornschein type of CSNB.
The cone photopic ERG is moderately altered in iCSNB patients, while markedly reduced in cCSNB [52, 53]. Therefore, we investigated the cone circuitry function under photopic (light adapted) conditions to confirm APLP2-KO as a model of iCSNB. Because photopic a-waves are negligible in mice , the amplitude and implicit time of the photopic b-waves were measured. The cone-mediated responses were recorded at a range of light intensities (−1.5 log to 1.5 log cds/m−2). With increasing flash intensities, the b-wave amplitude increased incrementally in both age groups but the maximal cone b-wave amplitude was significantly (p < 0.05) reduced in adult (97.1 ± 8.9 μV) compared to young WT (138.5 ± 8.5 μV) (Fig. 3d), consistent with age-related declines in cone function in C57BL/6 mice [55, 56]. In young, the maximal b-wave amplitude was significantly reduced (p < 0.05) in APLP2-KO (100.3 ± 7.8 μV) compared to WT (138.5 ± 8.5 μV) (Fig. 3d), indicating cone-mediated pathway dysfunction in young APLP2-KO. However, the b-wave implicit time was not altered in APLP2-KO compared to WT (data not shown). Moreover, the maximal amplitude of the cone ERG b-wave were comparable in both age groups for APLP2-KO mice (103 ± 7.8 μV vs. 87.7 ± 11.4 μV in young vs. adult, respectively) (Fig. 3e), indicating a non-progressive phenotype of APLP2-KO for cone dysfunction. Altogether these data indicate that loss of APLP2 in young and adult mice leads to an electrophysiological defect in retinal circuitry from the photoreceptors (rods and cones) to the bipolar cells resembling the iCSNB.
APLP2 is necessary for proper presynaptic ribbon and postsynaptic triad morphology of adult OPL
Cav1.4-KO mice show altered localization in the OPL of presynaptic proteins, including RIBEYE and PSD95, and impaired distribution of PNA-labeled cone pedicles . Further characterization of the OPL alteration in adult APLP2-KO mice was initially achieved using confocal microscopy and presynaptic marker antibodies to identify the photoreceptors. Four to six rows of RIBEYE-labeled rod ribbon and one row of clustering of RIBEYE at cone synaptic terminals (pedicles) were present in WT (Fig. 4a). In contrast, up to ten misaligned rows of disorganized rod ribbon synapses were detected in APLP2-KO OPL, suggesting the laminar restriction of rod presynaptic terminals (spherules) was compromised (Fig. 4b). The majority of RIBEYE-labeled ribbons showed non-accurate and punctuate-shaped structures, indicating signs of collapse of photoreceptor ribbons. Moreover, ectopic localization of RIBEYE-labeled structures was readily detected in large and numerous foci in the ONL (Fig. 4b). The laminar organization of the pedicles was also altered in APLP2-KO (Fig. 4b, arrows). While the RIBEYE staining in the APP-KO OPL was similar to WT, faint loci of RIBEYE-stained photoreceptor ribbon were observed deep within the ONL in APP-KO (Fig. 4c). In WT retina, one row of faint, aligned and regularly spaced horizontal (fluorescent-conjugated peanut agglutinin) PNA-stained cone pedicles was detected in the OPL (Fig. 4d). In contrast, PNA staining in APLP2-KO retina revealed the laminar restriction of cone pedicles was compromised (Fig. 4e). The PNA staining in APP-KO was similar to WT (Fig. 4f). We also monitored the expression of VGLUT1. VGLUT1 immunostaining was regular and dense in the OPL of WT and APP-KO (Fig. 4g and i). In contrast, APLP2-KO OPL had irregular VGLUT1 immunostaining (Fig. 4h). PSD-95 is used as a common marker for the photoreceptor presynaptic terminals  and has an atypical distribution in ribbon synapses. We observed a regular immunostaining pattern for PSD-95 in the OPL of WT and APP-KO (Fig. 4j and l). However, PSD-95 immunostaining was diffuse in the APLP2-KO OPL (Fig. 4k).
We next used TEM (16 K - 41 K x magnification) to monitor the photoreceptor terminals at the ultrastructure level. In the WT OPL region, the cone pedicles contained multiple triads composed of two lateral horizontal processes flanking a central bipolar cell dendrite (Fig. 4m). The majority of the rod spherules contained a unique long presynaptic ribbon and a visible arciform density at its base (Fig. 4n). In APLP2-KO, cone pedicles were irregular in shape and completely disorganized (Fig. 4o). Many rod spherules also displayed a densely stained retracting morphology (Fig. 4p, arrows). Moreover, many triads were misaligned and turned such that the presynaptic ribbon and the two lateral horizontal cells were laterally oriented (Fig. 4q, arrow), instead of facing the OPL (Fig. 4q, asterisk). At higher magnification (64 K x magnification), TEM of the few well-organized APLP2-KO synapses showed a unique long ribbon and a visible arciform density at its base (Fig. 4r), akin to WT synapses (Fig. 4n). In APP-KO, although the cones pedicles were not as well organized as in WT, they contained multiple well-developed triads (Fig. 4s). Higher magnification showed that the rod spherules still had a normal overall photoreceptor terminal architecture (Fig. 4t). Similar alterations of the presynaptic ribbon synapse and postsynaptic triad morphology, including disorganized rod spherules with misoriented synaptic ribbons (Additional file 1: Figure S4C and E, arrows), and irregular cone pedicles (Additional file 1: Figure S4D), were observed in young APLP2-KO.
APLP2 is necessary for the proper generation of bipolar cells and their dendritic branching and not horizontal cells
Next, we investigated alterations of the postsynaptic bipolar and horizontal cells in adult retinas by immunohistochemistry. Anti-Chx10 antibody, which specifically labels all the bipolar cells in adult retina, revealed large stained Chx10 nuclei of bipolar cells in the INL of all genotypes (Fig. 5a-c). Quantifying the number Chx10-positive cells identified a significant decrease (41.6 %) in APLP2-KO compared to WT, with no change in APP-KO (Fig. 5j). Gγ13, a specific marker for ON bipolar cells (rod bipolar and cone bipolar cells (types 5a and 5b and types 6–9)) stained three rows of ON bipolar cell somas in the WT INL (Fig. 5d). In comparison, APLP2-KO had only one or two rows of ON bipolar cell somas (Fig. 5e) and the number of Gγ13-positive ON bipolar cells was significantly reduced (36.4 %) in the INL (Fig. 5j). In addition, the APLP2-KO Gγ13 labeled dendritic branches appeared diffuse and in some cases the cells appeared without processes on their outer surface (Fig. 5e, arrowheads). In contrast, the ON bipolar cell soma row structure, cell number and profuse dendritic branching was similar between APP-KO and WT retina (Fig. 5d, f and j). Rod bipolar cells, which were identified by PKCα staining, displayed a regular laminar structure in WT retina (Fig. 5g), while APLP2-KO rod bipolar cell somas were less structured and had a disorderly arrangement (Fig. 5h). There was a significant reduction (21.4 %) in the number of PKCα–positive rod bipolar cells in APLP2-KO compared to WT (Fig. 5j) and the dendritic branches were also less profuse (Fig. 5h, arrowheads). Unlike APLP2-KO, the rod bipolar cell soma structure, content and dendritic arborization was similar between APP-KO and WT (Fig. 5g, i and j). Since the rod bipolar cells utilize a metabotropic pathway to sense light-induced variations in photoreceptor glutamate release, we double immunostained for the metabotropic glutamate receptor mGluR6 and PKCα in the retina. The mGluR6 co-localized to the dendritic tips of rod bipolar cells in WT retina, but in the APLP2-KO retina, the mGluR6 staining was substantially diminished (Fig. 5l and m respectively). We also found differences in the distribution and number of recoverin-positive type 2 OFF-cone bipolar cell somas between WT INL, which appeared in a regular manner, while in the APLP2-KO INL, their were significantly fewer positively stained cells (63.4 % reduction; Fig. 5n and o, arrowheads, k). In contrast to bipolar cells, we saw no differences between WT and APLP2-KO retinas when comparing the number and morphology of horizontal cell somas stained for calbindin (Fig. 5k, p and q respectively) or in the morphology of the horizontal cell axons in the OPL region when staining with anti-neurofilament 200 (Fig. 5r and s). APLP2-KO retinas showed altered synapses with either mislocation (e.g. RIBEYE) or reduced expression (e.g. mGluR6) of synaptic components associated with reduced number of Chx10-positive bipolar cells. Therefore, we performed Western blotting that compares the levels of Chx10 and the two synaptic markers RIBEYE and mGluR6 in WT and APLP2 KO differentiated retinas (Fig. 5t). Western blot analysis showed reduced levels of Chx10 in protein extracts of PN5 and adult APLP2-KO mice compared with WT mice and thus confirms the microscopy and cell counting data showing reduced numbers of bipolar cells in APLP2 compared with WT mice (Fig. 5t and Additional file 1: Table S2). We observed reduced levels of mGLUR6 and increased levels of RIBEYE in adult APLP2-KO compared with WT and thus confirm the microscopy observations. Moreover, we observed reduced levels of mGluR6 and increased levels of RIBEYE levels in PN5 APLP2-KO compared with WT (Fig. 5t and Additional file 1: Table S2), suggesting synaptic alteration during postnatal development in APLP2-KO retinas.
APLP2 is required for the differentiation of bipolar cells during post-natal development through the correct combination of differentiation transcription factors
CSNB is present at birth. It was recently suggested that impaired development of photoreceptor synapses associated with defect in synaptic transmission contributes to vision impairment in two mouse models of iCSNB . Therefore, we hypothesized APLP2-KO have defects in the development of the OPL. First, we examined APLP2-KO retinas during development. Histological examination of APLP2-KO retinas from E14 to PN1 showed a normal structural organization of the retinas (Additional file 1: Figure S5 A-C). In WT PN5, the photoreceptors initiate ribbon synapse formation  and the OPL begins to form (Additional file 1: Figure S5D), however in APLP2-KO the OPL remained undefined (Additional file 1: Figure S5E).
Then, we investigated whether the observed delay in the development of the APLP2-KO OPL may be secondary to abnormal cell differentiation using markers for postnatal retina differentiation. We initially looked at VGLUT1 expression because it provides a distinct temporal sequence ordering between cones and rods in developing mouse OPL . In WT retina at PN5, VGLUT1 was first expressed with the onset of synaptogenesis in cone pedicles, when they invaded the OPL, yet fewer VGLUT1-positive cone terminals were observed in APLP2-KO (Fig. 6a, upper panel). At PN10, intense VGLUT1 immunostaining was observed in WT retina when the rod spherules invaded the OPL, whereas VGLUT1 immunostaining was weak and thin in APLP2-KO (Fig. 6a, middle panel). By PN15, the mouse retina is fully differentiated into its three nuclear layers and two plexiform layers. The OPL in PN15 WT retina showed a bright and intense band of VGLUT1-positive cone and rod terminals, whereas VGLUT1 immunostaining was weak and diffuse in APLP2-KO (Fig. 6a, lower panel). The observed delay in postnatal development of photoreceptor presynaptic terminals in the APLP2-KO retina was confirmed by the significant decrease in the brightness intensity level quantitated for VGLUT1 immunostaining at each PN5, PN10 and PN15 age group examined (Additional file 1: Table S3). Moreover, we investigated defects in the differentiation of bipolar cells during retinal development. Chx10 is the earliest known pan-bipolar cell marker and its levels peak during bipolar differentiation and persist through adulthood [60, 61]. At PN5 and PN10, Chx10 immunostaining levels in APLP2-KO were weaker in the INL (Fig. 6b), and the number of Chx10-positive nuclei of bipolar cells was significantly decreased by 55.1 and 33.4 % at PN5 and PN10 respectively as compared to WT (Additional file 1: Table S3). This was consistent with findings in the Western blot analysis (Fig. 5t). Islet1 expression was also examined since it is important for differentiation of bipolar cells . At PN5, PN10 and PN15, the number of Islet1-postive bipolar cells in the middle portion of the APLP2-KO INL was significantly reduced by 59.7, 36.0 and 29.7 %, respectively when compared to WT (Fig. 6c and Additional file 1: Table S3). This supports the model that APLP2 participates in bipolar cell differentiation. Then, we investigated the expression of photoreceptor cell and bipolar cell markers during postnatal development by Western blotting. (Additional file 1: Figure S5F). WT and APLP2-KO protein extracts of the PN5 retinas were probed for VGLUT1 and Islet1. We observed a reduction in the levels of VGLUT1 and Islet1 in the APLP2-KO retinas as compared with WT retinas. Quantification of the amounts of each protein from the Western blot confirmed the overall reduction of the bipolar cell and photoreceptor terminal markers in PN5 APLP2-KO retinas (Additional file 1: Table S3), which was consistent with findings in the immunohistochemistry assay.
To elucidate the molecular mechanisms underlying bipolar cell defects in APLP2-KO retinal development we analyzed at PN1 and PN10 the mRNA levels of the major basic helix-loop-helix (bHLH) (MATH3 and BHLHB5) and homeodomain (HD) (CHX10, VSX1 and OTX2) factors involved in the generation or differentiation of bipolar cells [63–67]. Using qRT-PCR we found that at PN1 CHX10 and MATH3, the two main factors that promote bipolar cell generation, were significantly downregulated in APLP2-KO compared with WT (Fig. 7). The three major transcription factors involved in the differentiation of bipolar cell subtypes, VSX1 (OFF cone bipolar cells) and BHLHB5 (type 2 OFF cone bipolar cells) and OTX2 (rod bipolar cells), were also significantly downregulated (Fig. 7). Interestingly at PN10 the HD factors CHX10, VSX1 and OTX2 were unchanged, while in contrast the bHLH factors MATH3 and BHLHB5 remained significantly downregulated in APLP2-KO (Fig. 7). Taken together, these data demonstrate that deletion of APLP2 induced impaired regulation of the temporal expression of a combination of intrinsic factors involved in the control of bipolar cell generation (early postnatal) and differentiation (late postnatal) during development.
APLP2 is necessary for the development of bipolar cell dendritic tips and the generation of the ON and OFF pathways through the proper development of bipolar cell terminals
Since rod bipolar cell dendrites contact photoreceptor terminals in the OPL by PN10, we investigated PKCα immunostaining of bipolar cell dendrites at this developmental stage. In WT, PKCα-labeled rod bipolar cells displayed their typical elongated cell somas in the INL and developed dendrites (Fig. 8a, arrowhead). In contrast, APLP2-KO had fewer rod bipolar cell somas were observed and the dendritic branches were non-existent (Fig. 8a, arrowhead). At PN15, the APLP2-KO dendritic branches were diffuse and in some cases cells lacked processes on their outer surface as compared to WT (Fig. 8b, arrowhead). Altogether, these data reveal a role for APLP2 in the differentiation of bipolar cells and development of their dendritic tips during postnatal development.
Expression of VGLUT1 in bipolar cell terminals presents a temporal sequence of expression from OFF to ON laminae during the differentiation of the IPL, in addition to be expressed in the ribbon synapses of photoreceptors in the OPL . Therefore, we investigated APLP2 and VGLUT1 colocalization during postnatal development and in differentiated WT retinas (Fig. 8c and C1). At PN5, VGLUT1 and APLP2 staining mainly colocalized in the IPL, indicating that APLP2 labels rod bipolar cell terminals and ON cone bipolar cell terminals (Fig. 8c). APLP2 weakly stained the OPL and no colocalization of APLP2 and VGLUT1 was observed because VGLUT1 is not expressed in the OPL at this developmental stage (Fig. 8c). At PN10, VGLUT1 and APLP2 staining colocalized in the OPL of WT mice (Fig. 8c). Moreover, staining for VGLUT1 was preferentially located in the OFF sublamina where it colocalized with APLP2 staining (Fig. 8c and C1, magnified region from PN10 IPL). This data confirms localization of APLP2 in bipolar cell terminals during postnatal development. In differentiated retinas (PN30), VGLUT1 and APLP2 still colocalized presynaptically in the OPL (Fig. 8c). VGLUT1 showed equal staining intensity in the bipolar cell terminals of the OFF and ON sublamina, and APLP2 and VGLUT1 colocalized in the two sublaminas (Fig. 8c and C1, magnified region from PN30 IPL). At PN5, PSD95 was mainly observed in the IPL (Fig. 8d). APLP2 and PSD95 colocalized at bipolar cell ribbon synapses (Fig. 8d), consistent with the postsynaptic localization of PSD95 in the IPL. At this stage, a weak PSD95 and APLP2 co-staining was observed in the OPL. Immunofluorescence double staining of APLP2 and PSD95 confirms localization of APLP2 in ribbon synapses of photoreceptor cells from PN10 to adult WT OPL (Fig. 8d).
APLP2 is strongly expressed in the two retinal synaptic layers, IPL and OPL, during postnatal development, and we observed a delay in the development of the APLP2-KO OPL. Therefore, we investigated VGLUT1 expression in the IPL to study the differentiation of the bipolar cell synapse, during postnatal development in APLP2-KO. In WT, discrete VGLUT1 immunostaining was first detected in the inner retina at PN5, whereas no VGLUT1 immunostaining was observed in APLP2-KO (data not shown). At PN10, WT staining for VGLUT1 was preferentially located in the OFF sublamina where the bipolar cell terminals were located (Fig. 8e). In PN10 APLP2-KO there was more intense VGLUT1 immunostaining and an abnormal stratification pattern with two strong VGLUT1-stained sublaminae separated from each other by a large and weakly stained VGLUT1 band (Fig. 8e). Quantitative analysis of the confocal images in the OFF and ON sublaminae showed a significant increase of VGLUT1 immunostaining in APLP2-KO compared to WT (Additional file 1: Table S4). At PN30, VGLUT1 showed equal staining intensity in the bipolar cell terminals of the OFF and ON sublamina in WT (Fig. 8e and Additional file 1: Table S4). In contrast, VGLUT1 staining was less prominent in the OFF sublamina than in the ON lamina of APLP2-KO (Fig. 8e and Additional file 1: Table S4), consistent with poor cone OFF differentiation showed above. Overall, these data showed that deletion of APLP2 was associated with altered development of bipolar cell terminals in the IPL suggesting APLP2 expression is necessary for the correct generation of the ON and OFF pathways.
Activation of microglial cells occurs during postnatal development to phagocytose inappropriate synapses to form a regular array in the two retinal plexiform layers . Given the altered OPL and IPL in APLP2-KO, we hypothesized a change in microglial activation in these mice. WT retinas displayed no F4/80 immunostaining within the ONL, and rare immunostaining in the inner retinal layers. In contrast, processes of activated microglial cells were observed in the two plexiform layers and rarely in the INL of APLP2-KO (Additional file 1: Figure S6A). Classical complement cascade proteins have emerged as critical mediators of synaptic refinement. C1q refines the developing visual system through C3-dependent microglial phagocytosis of synapses . We hypothesized alteration of the expression levels of the complement cascade in APLP2-KO. qRT-PCR data analysis showed C1qa, C1qb and C3 were significantly upregulated (by 45.3, 33.0 and 177.5 fold respectively) in the retina of APLP2-KO compared with WT, indicating overactivation of the complement cascade in adult APLP2-KO (Additional file 1: Figure S6B).
Altered transcription of specific pre- and postsynaptic proteins in APLP2-KO
Although CSNB is a synapse pathology, the transcriptional consequences on genes encoding pre- and postsynaptic proteins of gene mutations responsible of CSNB remain unknown. Therefore, we hypothesized that deleting APLP2 may affect a transcriptional network essential for retinal synapse structure/function. To gain insights into the molecular mechanisms underlying synaptic defects in APLP2-KO, we analyzed mRNA expression of 12 proteins specifically involved in synaptic organization and function (Fig. 9a). In adult APLP2-KO retinas, 8 of the 12 genes coding for presynaptic proteins were significantly upregulated (Fig. 9b): RIBEYE (93-fold, major component of the photoreceptor ribbon synapses); L1CAM (13-fold, necessary to establish precise synaptic contacts; bassoon (10-fold, main scaffold protein of the active zone that regulates stability of Munc13-1 and SNAP25); active zone-associated calcium channel Cav1.4 (4-fold, necessary for maintaining bassoon in the ribbon synapse). Two main components of the soluble NSF attachment protein receptors, SNAP25 and syntaxin-1, were also upregulated. As were genes coding for two principal calcium sensors on synaptic vesicles, synaptotagmin 1 and Munc13-1 (2- to 3-fold). Genes coding for the presynaptic proteins: synapsin 2, PSD-95, synaptobrevin 2/VAMP2 and Munc18 had similar expression levels between WT and APLP2-KO.
In ON-bipolar cells, transmission of the light signal is mediated by GOα. In the dark, mGluR6 is constantly stimulated by glutamate and activates Goα which closes the TRPM1 channel, and PKCα accelerates and terminates glutamate-driven signal transduction. With the exception of TRPM1, which was significantly upregulated (9-fold), the other components of the ON bipolar cell signalling including mGluR6, GOα and PKCα were all significantly down regulated in APLP2-KO (Fig. 9b).
Non-redundant roles for APLP2 and APP in the retina
The changes seen in synapse structure in the APLP2-KO retina are novel and are in contrast to the absence of synapse alterations in the APLP2-KO parasympathetic submandibular ganglion in the salivary duct , and the APLP2-KO neuromuscular junction in the diaphragm and sternomastoid muscles . Sequence and phylogenetic analysis suggests there is functional conservation between APP and APLP1, but APLP2 having significantly diverged from both APP and APLP1 [5, 72]. Unlike other studies demonstrating that loss of APLP2 results in no gross abnormalities in the brain or PNS, we provide the first clear demonstration that APLP2 induces a profound phenotypic difference from APP. Our data have clearly identified non-redundant functions between APLP2 and APP in the adult retina and would indicate a specific role for APLP2 in retinal synaptogenesis and synaptopathy. Our data are consistent with recent data showing distinct and essential role of APLP2 at neuromuscular junction synapses that cannot be compensated by APP .
The exact molecular mechanism by which APLP2 is essential for synapse formation and function in the CNS remains to be determined. One could formulate several hypotheses regarding how APLP2 affects retinal synaptogenesis and the transmission of the light signal from the photoreceptors to the bipolar cells. APP/APLP has been identified as a novel class of synaptic adhesion molecules with shared properties as SynCAMs and neuroligins/neurexins . Roles of adhesion in the development and function of photoreceptor synapses remain incompletely understood. Unlike neuroligins [74, 75] or other immunoglobulin-family proteins, such as DSCAMs , that contribute to the development and function of the IPL, SynCAM 1 in the retina appears predominantly to provide for the structural and functional integrity of photoreceptor synapses in the OPL. SynCAM 1 is expressed on mouse rod photoreceptors and their terminals in the OPL in a developmentally regulated manner . In adult, SynCAM 1 is expressed in OPL, where it encircles VGLUT1-positive photoreceptor terminals. Interestingly, the structural integrity of synapses in the OPL is impaired in SynCAM 1-KO mice . Moreover, the number of ribbon-containing rod terminals was significantly lower and ribbons were shorter terminals with triads in SynCAM 1-KO mice, resembling retinal phenotype of APLP2-KO mice. Moreover, visual signal transmission in the scotopic (rod) pathway is impaired in SynCAM 1-KO mice. Consequently, APLP2 might play a SynCAM1-like synaptic adhesion function for OPL synaptogenesis and function. Besides a direct role in retinal synaptic adhesion, APP/APLP has been shown to interact with contactin 4 in the retina to promote NgCAM-dependent axon growth of ganglion cells in the chick . Moreover, a subset of direction-selective ganglion cells fail to target the nucleus of the optic tract in APP-KO or contactin 4-KO mice . Although these studies were limited to eye-to-brain connections, interactions of APLP2 with synaptic/cell adhesion molecules, including contactins, might be a mechanism by which APLP2 participates in OPL synaptogenesis, consistent with the identification of contactin 4 as a genetic marker of murine bipolar cells . The third hypothesis is that APLP2 might directly or indirectly affect expression of other proteins. Unfortunately, no transcriptome profiling of retina in knockout mice lacking APP family members is available. However, the comparative transcriptome profiling of APP family members in adult cortex revealed that of 1061 genes that are altered after deletion of APLP2, only 17 % are also changed in APP-KO . Moreover, brain interactomes for APLP2 and APP are different . These studies suggest there are distinct pathways regulated by either APP or APLP2, consistent with the different APP and APLP2 retinal phenotypes. Among the nine APLP2-specific interactors identified in the brain , four are of potential interest because of their involvement in retinal development or retinal disorder: Retinitis Pigmentosa 2 homolog (RP2h), Ras-related C3 botulinum substrate 1 (RAC1), Protein phosphatase 2A (PP2A) and Rho family GTPase (RhoA). Mutation in the human RP2 gene cause X-linked retinitis pigmentosa [83, 84]. The Rp2h-KO mice showed significant reductions of the a-wave and b-wave amplitudes at 1 month of age and continued to decline over the next 6 months and exhibited a slowly progressing rod-cone dystrophy by 8 months . In Rac1-KO mice, the numbers of cells in the ganglion cell layer and the INL are reduced to 50 % of the WT level, but the ONL is largely unaffected , implying a central role for Rac1in inner retinal development. PP2A dephosphorylates CaBP4 in the mouse retina . Mutations in CABP4 lead to iCSNB and mice lacking either Cabp4 display a iCSNB-like phenotype . CaBP4 directly associates with the Cav1.4α channel. Increased CaBP4 phosphorylation potentiates the modulatory effect of CaBP4 on Cav1.3 Ca(2+) channels. RhoA signaling maintains apico-basal polarity in retinal progenitor cells, which is essential for subsequent cellular differentiation . No retinal pathology has been described with RhoA dysfunction, so far.
Molecular mechanisms underlying synaptic defects in APLP2-KO and animal models of CSNB
Although for different genes the pathogenic mechanisms of CSNB has been identified, for others further studies are needed to clarify the molecular mechanisms of CSNB. Loss-of-function mutations in some synaptic genes are responsible for alteration of the neurotransmission from photoreceptors to bipolar cells in iCSNB . APLP2 localizes at both the dendrites of the bipolar cells and the presynatic terminals of the photoreceptors. Moreover, histology, immunohistochemistry and TEM of APLP2-KO retinas showed alterations on both the presynaptic terminals of rods and cones, and the dendritic tips of the bipolar cells, making APLP2-KO a pathology of both the pre- and postsynatic part of the OPL.
Analysis of the expression of pre- and postsynatic genes in CSNB and animal models of CSNB has been rarely performed to identify the molecular mechanism involved or associated with the pathogenic events in CSNB. The transcriptome analysis of the genes coding pre- and postsynaptic proteins in APLP2-KO retinas, indicates enrichment of genes important for presynaptic function/organization ─ RIBEYE, Bassoon, Munc13, Syntaxin1, SNAP25, Synaptogamin-1, Cav1.4, L1CAM, TRPM1, and impoverishment of postsynaptic genes ─ mGluR6, Gα0 and PKCα (summarized in the schema, Fig. 9a). Deletion of APLP2 also results in a severe reduction of mGluR6 at the dendritic tips of rod bipolar cells. Therefore, our study showed a reduction in the expression of major components of the mGluR6 signaling cascade in APLP2-KO. Interestingly, GRM6- and NYX- and LRIT3 deficient mouse, three models for cCSNB, showed a nearly absent mGluR6 at the dendritic tips of cone ON-bipolar cells [71, 89–91], indicating a reduction in ON-bipolar cells of major components of the mGluR6 signaling cascade in mouse models of cCSNB. By RT-qPCR, we demonstrated that APLP2 deletion alters the expression of TRPM1, GRM6 and CACNA1F, three major genes involved in CSNB. This suggests that even in the absence of any mutation, APLP2 may be involved in the phenotype of CSNB by its regulation function of expression of genes directly involved in this pathology. Recently, a new naturally occurring animal model of cCSNB has been characterized in beagle dog . All known CSNB genes have been excluded in this model. However, a reduction in the expression of the photoreceptor postsynaptic gene PKCA and an increased expression of the photoreceptor postsynaptic gene TRPM1 were observed in this model, as we observed in APLP2-KO mice. It remains to investigate the expression of APLP2 in this model.
New roles for retinal differentiation genes in CSNB?
APLP2 deletion alters the expression of bHLH and HD transcription factors that are involved in the generation and differentiation of bipolar cells at early and late postnatal stages of development. Since CSNB is present at birth and ERG b-wave is reduced in mice either lacking Bhlhb4 or Math5, two transcription factors required for maturation/differentiation of bipolar cells, it was suggested that altered differentiation of bipolar cells may be involved in the phenotype of CSNB [44, 45]. Recently, the differentiation factor, PRDM8, was presented as a candidate gene for CSNB , reinforcing the importance to study the mechanisms of bipolar cell differentiation for elucidating the pathological events involved in CSNB. ON-bipolar (G0α-positve cells), rod bipolar (PKC-positive cells) and type 2 (recoverin-positive cells) cone bipolar cells were markedly reduced in PRDM8-KO mice . Reduced VGLUT1 staining was also observed in the IPL of PRDM8-KO mice. Moreover, a reduced scotopic b-wave amplitude with a normal a-wave amplitude was observed in PRDM8-KO mice . The ERG deficits of PRDM8-KO mice were stationary between 3 and 6 months of age. The stationary ERG phenotype of APLP2-KO mice was observed between 2–4 months and 6–13 months of age. An additional role of APLP2 in the retina is the control of bipolar cell (ON-bipolar, rod bipolar and type 2 cone bipolar cells) differentiation, development of bipolar cell dendrites, temporal sequence of VGLUT1 expression from OFF to ON laminae during the differentiation of the IPL and the formation of cone and rod ribbon synapses during postnatal development. Therefore, we cannot rule out that APLP2 may also be involved in CSNB phenotype by its function of differentiation factor. This is in accordance with the recently suggested role of LRIT3 in cone synapse formation , confirming the importance of photoreceptor synaptogenesis in CSNB. However, alteration of ribbon synapse formation or bipolar dendrite invagination has been described in GRM6 mutants and Gβ5-KO mice, two models of cCSNB [92–95]. Moreover, Cav1.4 and CaBP4-KO mice exhibit altered photoreceptor synaptogenesis , confirming that impaired retinal differentiation contributes to vision impairment in CSNB. It remains to be determined if APLP2 expression is altered in the bipolar cells and photoreceptor ribbon synapses of GRM6-, TRPM1-, NYX-, GRP179-, Cav1.4-, CaBP4- or LRIT3-KO mice during development and in adults.
The homozygous APP and APLP2 knockout and wild-type (C57/Bl6) mice have been described [96–98]. Eye balls were harvested from mice at different ages ranging from embryonic day (E) 14 and E18, and postnatal day (PN) 1, 5, 10, and 15, and from young (2–4 months) and adult (6–13 months). All Procedures were approved by the Animal Ethics Committee at the Pierre et Marie University and Paris-Descartes University of Paris and were carried out in accordance with French laws and the European Union Directive 2010/63/EU.
In vivo assessment of mice retinal thickness was performed on anesthetized animals using spectral domain optical coherence tomography (SD-OCT) (Spectralis, Heidelberg Engineering) adapted for small animal eyes. Temporal, nasal, and superior quadrants of the retina were analyzed, using the optic nerve head and the retina vessels as landmarks. Each 2-dimensional B-scan recorded at 30° field of view consisted of 1536 A-scans with an optical resolution reaching 3.5 μm. Thickness of full retina, inner retina, and ONL were quantified using software provided by Heidelberg Engineering (Heidelberg Eye Explorer Version 126.96.36.199).
Measurement of retinal thickness
Retina cross-sections were mounted and stained with toluidine blue. Images of whole retina cross-sections were obtained using Leica leitz Aristoplan microscope equipped with DFC 480 camera (Leica) and LAS 3.7 version software. Thickness of the different nuclear and synaptic layers were determined using Visilog 6.4 version software (Noesis).
Retinal expression of APLP2 during embryonic and postnatal development was investigated by immunohistochemistry as previously described . Serial eye sections were stained with primary rabbit anti-APLP2 antibody and detected with a secondary antibody, a goat polyclonal biotin-conjugated anti-rabbit IgG (1/1000, Vector Laboratories) and visualized using streptavidin and biotinylated horseradish peroxidase complex (sABC) and diaminobenzidine tetrahydrochloride (DAB). The peroxidase-stained sections were viewed with an Aristoplan-microscope (Zeiss) connected to a digital camera.
Identification and visualization of specific cells and cellular structures in the retina was performed by immunofluorescence microscopy as previously described . Primary antibodies are shown in Additional file 1: Table S1. Control experiments to check specificity of the primary antibodies: APLP2 antibody was omitted and secondary antibody was tested. Retinas of at least three animals were used at each stage. Nuclei were counterstained with DAPI (1:4000, Sigma-Aldrich). Sections were mounted with Dako (Cytomation). Slides were observed with a Zeiss confocal Imaging system (LSM710, Zeiss). All immunostaining was repeated at least three times. To quantify the number of different cell-type markers on retinal sections, three or more age-matched retinas were analyzed for each cell type. At least five non-overlapping fields of 400 μm of linear retinal length were photographed and printed at 40X magnification. They were counted from each retina section (4 or more sections per animal) and averaged per group.
Transmission electron microscopy
After dissection, retinas were fixed in 2.5 % glutaraldehyde cacodylate buffer (0.1 M, pH 7.4) and then fixed in 1 % osmium tetroxyde in cacodylate buffer (0.2 M, pH 7.4) and progressively dehydrated in graduated ethanol solution, then in propylene oxide. Semi-thin sections (1 μm) were cut with an ultra microtome (Reichert OmU2) and stained with toluidine blue. Ultra-thin sections (80 nm) were contrasted by uranyl acetate, and analyzed with a transmission electron microscope (Philips CM10).
Western blot analysis
Retinas were lysed in ice-cold lysis buffer (50 mM Tris–HCl, pH 7.5, 100 mM NaCl, 0.1 % NP-40, 1 % deoxycholate, 50 mM β-glycerophosphate, 0.2 mM sodium orthovanadate, 50 mM sodium fluoride, 1 μg/mL leupeptin, 5 μM pepstatin, 20 kIU/mL aprotinin, 1 mM phenylmethylsulfonyl fluoride), and centrifuged for 10 min at 10,000 g at 4 °C. Protein concentrations were determined using a Bio-Rad kit. Retina lysates were mixed with 3× Laemmli buffer and heated for 5 min at 95 °C. They were then resolved by SDS-PAGE (10 % or 15 % polyacrylamide gels), electroblotted onto polyvinylidene difluoride (PVDF) membrane (Immobilon; Millipore), and probed with antibodies directed against Chx10, Islet1, VGLUT1, RIBEYE mGluR6 and actin (Additional file 1: Table S1). Primary antibodies were tagged with specific secondary horseradish peroxidase-conjugated antibodies. Antibody complexes were detected by enhanced chemiluminescence (ECL; Amersham), and the membrane was placed against Kodak film (BioMax Light-1; Eastman Kodak). Quantification was carried out using a Kodak image station (2000 MM) and Kodak software (1D3.6).
Quantitative real-time PCR
Mouse retina tissue was exposed to TRIZOL reagent (Invitrogen, France) according to the manufacturer’s instructions, and SuperScript II Reverse Transcriptase (Invitrogen) was used to reverse transcribe 1 μg of mRNA. Amplification reaction assays contained 1× SYBR Green PCR Mastermix (Applied Biosystems). All real-time PCR oligonucleotide primers had previously been validated experimentally by qPCR, agarose gel analysis, sequencing, and blast. The PCR primer sequences are available on request. A hot start at 95 °C for 5 min followed by 40 cycles at 95 °C for 15 s and 60 °C for 1 min with the 7300 SDS thermal cycler (Applied Biosystems). Controls with no reverse transcriptase were run for each assay to confirm the absence of genomic DNA contamination. Control qRT-PCRs were performed without cDNA templates. The standard curve method (Prism 7700 Sequence Detection System, Applied Biosystems, ABI User Bulletin number 2) was used for relative quantification of gene expression. For each experiment, each individual sample was run in triplicate and the C t value for each sample recorded at the end of the reaction. The average and standard deviation of the three C t values were calculated. Gene expression levels were normalized to β-actin for each retinal tissue sample and calculated relative to WT retinal tissue with the following equation: relative expression = 2─(APLP2 sample ΔCt ─ WT sample ΔCt) where ΔC t = mean C t(target) − mean C t(β-actin).
Animals were dark adapted overnight. Under dim-red-light, they were anesthetized with a mixture of ketamine/xylazine and their pupils dilated with 1 drop of atropine. A photostimulator (Type PS 33) was used to generate ERG. The highest flash stimulation was 11.8 cd.s.m2 and neutral density filter were used to attenuate luminance. Flash stimuli were given through an integrative sphere in order to uniformly illuminate all retina. A single ERG was recorded for seventeen increasing luminance (10 μs duration, 30s apart) via Ag/AgCl electrodes. The signal was amplified (gain 1000, pass band 0.1-10,000 Hz; A-M systems, Inc; Model 3000. AC/DC Differential Amplifier) then processed and stored in a computer. For each ERG, a- and b-wave amplitude and latency were calculated. The mean values are plotted against the flash stimulation luminance. The software program (Microsoft Origin 6.0; Microcal Software) was used to fit the b-wave sensitivity curves to calculate the saturated b-wave amplitude (B max), the half-saturation luminance (K); and the slope of the curve in its linear part (n). For photopic conditions, mice were light-adapted 10 min at 30 cd/s m2 and then the retinal activity recorded in response to single flashes ranging from 10−2 to 30 cds/m2, in the same illumination conditions. For each stimulus intensity, 10 to 15 traces were averaged. Amplitude of the a-wave was defined as the difference between the baseline level at the time of stimulation and the peak of the a-wave. Amplitude of the b-wave was defined as the difference between the peak of the b-wave and the peak of the a-wave (or the baseline level when the a-wave was not detectable). Amplitudes are expressed in μV.
All data are presented as mean ± s.e.m. Statistical significance in pairwise comparisons was assessed using two-tailed t-tests with unequal variance.
In conclusion, our findings demonstrated the important and specific role of APLP2 in the retina. Our results demonstrate the non-redundant actions of APLP2 and APP in the central nervous system that are mediated through different effects on specific neurons and on ribbon synaptic networks during late embryonic and early postnatal development. Most importantly and of clinical relevance, there are striking similarities to be found between the phenotypic features of bipolar cell dendrites and photoreceptor ribbon synapses, and vision alteration in APLP2-KO mice and congenital stationary night blindness. APLP2 may be a bridge between retina development and synaptic genes involved in the pathogenic events in CSNB. Our studies have identified APLP2 as a new molecule that warrants investigation for its involvement in a range of eye pathologies.
APLP2, amyloid precursor-like protein 2; APP, amyloid precursor protein; BHLH, basic helix-loop-helix; BHLHB4, basic helix-loop-helix domain containing, class B 4; C1q, complement 1 q; CABP4, calcium binding protein 4; CACNA1F/Cav1.4, calcium channel, voltage-dependent, L type, alpha 1 F subunit; cGMP, cyclic guanosine monophosphate; Chx10, Ceh-10 homeodomain-containing homolog; CNS, central nervous system; CSNB, congenital stationary night blindness; DSCAM, down syndrome cell adhesion molecule; ERG, electroretinogram; GCL, ganglion cell layer; Gγ13, G protein gamma 13 subunit; HD, homeodomain; INL, inner nuclear layer; IPL, inner plexiform layer; IS, inner segment; Islet1, insulin related protein 1; L1CAM, L1 cell adhesion molecule; LRIT3, Leucine-rich repeat, immunoglobulin-like and transmembrane domains 3; MATH5/ATOH7, atonal BHLH transcription factor 7; mGluR6, metabotropic glutamate receptor 6; mRNA, messenger ribonucleic acid; NBL, neuroblastic layer; NFL, nerve fiber layer; NYX, nyctalopin; OCT, optical coherence tomography; OLM, outer limiting membrane; ONL, outer nuclear layer; OPL, outer plexiform layer; OS, outer segment; OTX2, orthodenticle homeobox 2; PKCα, protein kinase C alpha; PN, postnatal day; PNA, peanut agglutinin; PNS, peripheral nervous system; PP2A, Protein phosphatase 2A; PRDM8, RIZ homology domain containing 8; PSD95, postsynaptic density protein 95; RAC1, Ras-related C3 botulinum substrate 1; RGC, retinal ganglion cells; RhoA, Rho family GTPase; RP2h, Retinitis Pigmentosa 2 homolog; RPE, retinal pigment epithelium; RT-PCR, reverse transcription polymerase chain reaction; SD-OCT, spectral domain optical coherence tomography; SNAP25, synaptosomal-associated protein 25; SynCAM, synaptic cell adhesion molecule; TEM, transmission electron microscopy; TRPM1, transient receptor potential cation channel subfamily M member 1; VGLUT1, vesicular glutamate transporter 1; VSX1, visual system homeobox 1; WT, wild-type; XRLS, X-linked Retinoschisis
Cappai R, Barnham KJ. Delineating the mechanism of Alzheimer’s disease A beta peptide neurotoxicity. Neurochem Res. 2008;33(3):526–32.
De Strooper B, Iwatsubo T, Wolfe MS. Presenilins and γ-secretase : structure, function, and role in Alzheimer disease. Cold Spring Harb Perspect Med. 2012;2(1):a006304.
Müller UC, Zheng H. Physiological functions of APP family proteins. Cold Spring Harb Perspect Med. 2012;2:a006288.
Yankner BA, Dawes LR, Fisher S, Villa-Komaroff L, Oster-Granite ML, Neve RL. Neurotoxicity of a fragment of the amyloid precursor associated with Alzheimer’s disease. Science. 1989;245(4916):417–20.
Shariati SA, De Strooper B. Redundancy and divergence in the amyloid precursor protein family. FEBS Lett. 2013;587:2036–45.
Tkatchenko AV, Tkatchenko TV, Guggenheim JA, Verhoeven VJ, Hysi PG, Wojciechowski R, et al. APLP2 regulates refractive error and myopia development in mice and humans. PLoS Genet. 2015;11(8):e1005432.
Ohta M, Kitamoto T, Iwaki T, Ohgami T, Fukui M, Tateishi J. Immunohistochemical distribution of amyloid precursor protein during normal rat development. Brain Res Dev Brain Res. 1993;75:151–61.
Salbaum JM, Ruddle FH. Embryonic expression pattern of amyloid protein precursor suggests a role in differentiation of specific subsets of neurons. J Exp Zool. 1994;269:116–27.
Shariati SA, Lau P, Hassan BA, Müller U, Dotti CG, De Strooper B, et al. APLP2 regulates neuronal stem cell differentiation during cortical development. J Cell Sci. 2013;126:1268–77.
Morgans CW, Zhang J, Jeffrey BG, Nelson SM, Burke NS, Duvoisin RM, et al. TRPM1 is required for the depolarizing light response in retinal ON-bipolar cells. Proc Natl Acad Sci U S A. 2009;106(45):19174–8.
Shen Y, Heimel JA, Kamermans M, Peachey NS, Gregg RG, Nawy S. A transient receptor potential-like channel mediates synaptic transmission in rod bipolar cells. J Neurosci. 2009;29(19):6088–93.
Koike C, Obara T, Uriu Y, Numata T, Sanuki R, Miyata K, et al. TRPM1 is a component of the retinal ON bipoalr cell transduction channel in the mGluR6 cascade. Proc Natl Acad Sci U S A. 2010;107(1):332–7.
Dhingra A, Lyubarsky A, Jiang M, Pugh Jr EN, Birnbaumer L, Sterling P, et al. The light response of ON bipolar neurons requires G[alpha]o. J Neurosci. 2000;20(24):9053–8.
Dhingra A, Jiang M, Wang TL, Lyubarsky A, Savchenko A, Bar-Yehuda T, et al. Light response of retinal ON bipolar cells requires a specific splice variant of Galpha(o). J Neurosci. 2002;22(12):4878–84.
Dhingra A, Vardi N. mGlu receptors in the retina-WIREs membrane transport and signaling. Wiley Interdiscip Rev Membr Transp Signal. 2012;1(5):641–53.
Ray TA, Heath KM, Hasan N, Noel JM, Samuels IS, Martemyanov KA, et al. GRP179 is required for high sensitivity of the mGluR6 signaling cascade in the depolarizing bipolar cells. J Neurosci. 2014;34(18):6334–43.
Neuillé M, El Shamieh S, Orhan E, Michiels C, Antonio A, Lancelot ME, et al. Lrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB). PLoS ONE. 2014;9(3):e90342.
Dinet V, An N, Ciccotosto GD, Bruban J, Maoui A, Bellingham SA, et al. APP involvement in retinogenesis of mice. Acta Neuropathol. 2011;121:351–63.
Ho T, Vessey KA, Cappai R, Dinet V, Mascarelli F, Ciccotosto GD, et al. Amyloid precursor protein is required for normal function of the rod and cone pathways in the mouse retina. PLoS ONE. 2012;7:e29892.
Rosner M, Hefetz L, Abraham FA. The prevalence of retinitis pigmentosa and congenital stationary night blindness in Israel. Am J Ophthalmol. 1993;116:373–4.
Dryja TP. Molecular genetics of oguchi disease, fundus albipunctatus, and other forms of stationary night blindness :LVII Edward Jackson Memorial lecture. Am J Ophthalmol. 2000;30(5):547–63.
Zeitz C, Forster U, Neidhardt J, Feil S, Kälin S, Leifert D, et al. Night blindness-associated mutations in the ligand-binding, cysteine-rich, and intracellular domains of the metabotropic glutamate receptor 6 abolish protein trafficking. Hum Mutat. 2007;28(8):771–80.
Zeitz C, Robson AG, Audo I. Congenital stationary night blindness: an analysis and update of genotype-phenotype correlations and pathogenic mechanisms. Prog Retin Eye Res. 2015;45:58–110.
Riggs LA. Electrretinography. Vision Res. 1983;26(9):1443–59.
Schubert G, Bornschein H. Analysis of the human electroretinogram. Ophthalmologica. 1952;123:396–413.
Miyake Y, Yagasaki K, Horiguchi M, Kawase Y, Kanda T. Congenital stationary night blindness with negative electroretinogram. A new classification. Arch Ophthalmol. 1986;104:1013–20.
Bech-Hansen NT, Naylor MJ, Maybaum TA, Sparkes RL, Koop B, Birch DG, et al. Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness. Nat Genet. 2000;26:319–23.
Pusch CM, Zeitz C, Brandau O, Pesch K, Achatz H, Feil S, et al. The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein. Nat Genet. 2000;26(3):324–7.
Dryja TP, McGee TL, Berson EL, Fishman GA, Sandberg MA, Alexander KR, et al. Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6. Proc Natl Acad Sci U S A. 2005;102:4884–9.
Zeitz C, Minotti R, Feil S, Matyas G, Cremers FP, Hoyng CB, et al. Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindness. Mol Vis. 2005;11:179–83.
Audo I, Kohl S, Leroy BP, Munier FL, Guillonneau X, Mohand-Saïd S, et al. TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness. Am J Hum Genet. 2009;85(5):720–9.
Li Z, Sergouniotis PI, Michaelides M, Mackay DS, Wright GA, Devery S, et al. Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans. Am J Hum Genet. 2009;85:711–9.
Zeitz C, Jacobson SG, Hamel CP, Bujakowska K, Neuillé M, Orhan E, et al. Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness. Am J Hum Genet. 2013;92(1):67–75.
Strom NT, Nyakatura G, Apfelstedt-Sylla E, Hellebrand H, Lorenz B, Weber BH, et al. An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness. Nat Genet. 1998;19:260–3.
Bech-Hansen NT, Naylor MJ, Maybaum TA, Pearce WG, Koop B, Fishman GA, et al. Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness. Nat Genet. 1998;19:264–7.
Vincent A, Héon E. Outer retinal structural anomaly due to frameshift mutation in CACNA1F gene. Eye (Lond). 2012;26(9):1278–80.
Chen RW, Greenberg JP, Lazow MA, Ramachandran R, Lima LH, Hwang JC, et al. Autofluorescence imaging and spectral-domain optical coherence tomography in incomplete congenital stationary night blindness and comparison with retinitis pigmentosa. Am J Ophthalmol. 2012;153(1):143–54.
Zeitz C, Kloeckener-Gruissem B, Forster U, Kohl S, Magyar I, Wissinger B, et al. Mutations in CABP4, the gene encoding the Ca2 + −binding protein 4, cause autosomal recessive night blindness. Am J Hum Genet. 2006;79(4):657–67.
Bijveld MM, Florijn RJ, Bergen AA, van den Born LI, Kamermans M, Prick L, et al. Genotype and phenotype of 101 dutch patients with congenital stationary night blindness. Ophthalmology. 2013;120(10):2072–81.
Khan AO, Alrashed M, Alkuraya FS. Clinical characterisation of the CABP4-related retinal phenotype. Br J Ophthalmol. 2013;97(3):262–5.
Lodha N, Loucks CM, Beaulieu C, Parboosingh JS, Bech-Hansen NT. Congenital stationary night blindness: mutation update and clinical variability. Adv Exp Med Biol. 2012;723:371–9.
Liu X, Kerov V, Haeseleer F, Majumder A, Artemyev N, Baker SA, et al. Dysregulation of Ca(v)1.4 channels disrupts the maturation of photoreceptor synaptic ribbons in congenital stationary night blindness type 2. Channels (Austin). 2013;7(6):514–23.
Knoflach D, Kerov V, Sartori SB, Obermair GJ, Schmuckermair C, Liu X, et al. Cav1.4 IT mouse as model for vision impairment in human congenital stationary night blindness type 2. Channels (Austin). 2013;7(6):503–13.
Bramblett DE, Pennesi ME, Wu SM, Tsai MJ. The transcription factor Bhlhb4 is required for rod bipolar cell maturation. Neuron. 2004;43(6):779–93.
Brzezinski 4th JA, Brown NL, Tanikawa A, Bush RA, Sieving PA, Vitaterna MH, et al. Loss of circadian photoentrainment and abnormal retinal electrophysiology in Math5 mutant mice. Invest Ophthalmol Vis Sci. 2005;46(7):2540–51.
Jung CC, Atan D, Ng D, Ploder L, Ross SE, Klein M, et al. Transcription factor PRDM8 is required for rod bipolar and type 2 OFF-cone bipolar cell survival and amacrine subtype identity. Proc Natl Acad Sci U S A. 2015;112(23):E3010–9.
Kondo M, Das G, Imai R, Santana E, Nakashita T, Imawaka M, et al. A Naturally Occurring Canine Model of Autosomal Recessive Congenital Stationary Night Blindness. PLoS ONE. 2015;10(9):e0137072.
Aydin D, Weyer SW, Müller UC. Functions of the APP gene family in the nervous system: insights from mouse models. Exp Brain Res. 2012;217:423–34.
Deutman AF, Pinckers AJ, Aan de Kerk AL. Dominantly inherited cystoid macular edema. Am J Ophthalmol. 1976;82:540–8.
George ND, Yates JR, Moore AT. Clinical features in affected males with X-linked retinoschisis. Arch Ophthalmol. 1996;114:274–80.
Tantri A, Vrabec TR, Cu-Unjieng A, Frost A, Annesley Jr WH, Donoso LA. X-linked retinoschisis: a clinical and molecular genetic review. Surv Ophthalmol. 2004;49(2):214–30.
Miyake Y, Horiguchi M, Ota I, Shiroyama N. Characteristic ERG-flicker anomaly in incomplete congenital stationary night blindness. Invest Ophthalmol Vis Sci. 1987;28(11):1816–23.
Quigley M, Roy MS, Barsoum-Homsy M, Chevrette L, Jacob JL, Milot J. On- and off-responses in the photopic electroretinogram in complete-type congenital stationary night blindness. Doc Ophthalmol. 1996;92(3):159–65.
Peachey NS, Goto Y, al-Ubaidi MR, Naash MI. Properties of the mouse cone-mediated electroretinogram during light adaptation. Neurosci Lett. 1993;162(1–2):9–11.
Gresh J, Goletz PW, Crouch RK, Rohrer B. Structure-function analysis of rods and cones in juvenile, adult, and aged C57bl/6 and Balb/c mice. Vis Neurosci. 2003;20(2):211–20.
Williams GA, Jacobs GH. Cone-based vision in the aging mouse. Vision Res. 2007;47(15):2037–46.
Zabouri N, Haverkamp S. Calcium channel-dependent molecular maturation of photoreceptor synapses. PLoS ONE. 2013;8(5):e63853.
Koulen P, Fletcher EL, Craven SE, Bredt DS, Wässle H. Immunocytochemical localization of the postsynaptic density protein PSD-95 in the mammalian retina. J Neurosci. 1998;18:10136–49.
Sherry DM, Wang MM, Bates J, Frishman LJ. Expression of vesicular glutamate transporter 1 in the mouse retina reveals temporal ordering in development of rod vs. cone and ON vs. OFF circuits. J Comp Neurol. 2003;465:480–98.
Burmeister M, Novak J, Liang MY, Basu S, Ploder L, Hawes NL, et al. Ocular retardation mouse cause by CHX10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation. Nat Genet. 1996;12:376–84.
Liu IS, Chen JD, Ploder L, Vidgen D, van der Kooy D, Kalnins VI, et al. Developmental expression of a novel murine homeobox gene (Chx10): evidence for roles in determination of the neuroretina and inner nuclear layer. Neuron. 1994;13:377–93.
Elshatory Y, Everhart D, Deng M, Xie X, Barlow RB, Gan L. Islet-1 controls the differentiation of retinal bipolar and cholinergic amacrine cells. J Neurosci. 2007;27:12707–20.
Tomita K, Nakanishi S, Guillemot F, Kageyama R. Mash1 promotes neuronal differentiation in the retina. Genes Cells. 1996;1:765–74.
Chow RL, Snow B, Novak J, Looser J, Freund C, Vidgen D, et al. Vsx1, a rapidly evolving paired-like homeobox gene expressed in cone bipolar cells. Mech Dev. 2001;109:315–22.
Hatakeyama J, Tomita K, Inoue T, Kageyama R. Roles of homeobox and bHLH genes in specification of a retinal cell type. Development. 2001;128:1313–22.
Feng L, Xie X, Joshi PS, Yang Z, Shibasaki K, Chow RL, et al. Requirement for Bhlhb5 in the specification of amacrine and cone bipolar subtypes in mouse retina. Development. 2006;133:4815–25.
Huang L, Hu F, Feng L, Luo XJ, Liang G, Zeng XY, et al. Bhlhb5 is required for the subtype development of retinal amacrine and bipolar cells in mice. Dev Dyn. 2014;243:279–89.
Hume DA, Perry VH, Gordon S. Immunohistochemical localization of a macrophage-specific antigen in developing mouse retina: phagocytosis of dying neurons and differentiation of microglial cells to form a regular array in the plexiform layers. J Cell Biol. 1983;97:253–7.
Stevens B, Allen NJ, Vazquez LE, Howell GR, Christopherson KS, Nouri N, et al. The classical complement cascade mediates CNS synapse elimination. Cell. 2007;131:1164–78.
Yang G, Gong YD, Gong K, Jiang WL, Kwon E, Wang P, et al. Reduced synaptic vesicle density and active zone size in mice lacking amyloid precursor protein (APP) and APP-like protein 2. Neurosci Lett. 2005;384:66–71.
Wang P, Yang G, Mosier DR, Chang P, Zaidi T, Gong YD, et al. Defective neuromuscular synapses in mice lacking amyloid precursor protein (APP) and APP-Like protein 2. J Neurosci. 2005;25:1219–25.
Gu X, Zou Y, Su Z, Huang W, Zhou Z, Arendsee Z, et al. An Update of diverge Software for Functional Divergence Analysis of Protein Family. Mol Biol Evol. 2013;30:1713–9.
Klevanski M, Saar M, Baumkötter F, Weyer SW, Kins S, Müller UC. Differential role of APP and APLPs for neuromuscular synaptic morphology and function. Mol Cell Neurosci. 2014;61:201–10.
Hoon M, Bauer G, Fritschy JM, Moser T, Falkenburger BH, Varoqueaux F. Neuroligin 2 controls the maturation of GABAergic synapses and information processing in the retina. J Neurosci. 2009;29(25):8039–50.
Hoon M, Soykan T, Falkenburger B, Hammer M, Patrizi A, Schmidt KF, et al. Neuroligin-4 is localized to glycinergic postsynapses and regulates inhibition in the retina. Proc Natl Acad Sci U S A. 2011;108(7):3053–8.
Fuerst PG, Bruce F, Tian M, Wei W, Elstrott J, Feller MB, et al. DSCAM and DSCAML1 function in self-avoidance in multiple cell types in the developing mouse retina. Neuron. 2009;64(4):484–97.
Ribic A, Liu X, Crair MC, Biederer T. Organization and function of mouse photoreceptor ribbon synapses involve the immunoglobulin protein synaptic cell adhesion molecule 1. J Comp Neurol. 2014;522(4):900–20.
Osterfield M, Egelund R, Young LM, Flanagan JG. Interaction of amyloid precursor protein with contactins and NgCAM in the retinotectal system. Development. 2008;135(6):1189–99.
Osterhout JA, Stafford BK, Nguyen PL, Yoshihara Y, Huberman AD. Contactin-4 mediates axon-target specificity and functional development of the accessory optic system. Neuron. 2015;86(4):985–99.
Kim DS, Ross SE, Trimarchi JM, Aach J, Greenberg ME, Cepko CL. Identification of molecular markers of bipolar cells in the murine retina. J Comp Neurol. 2008;507(5):1795–810.
Aydin D, Filippov MA, Tschäpe JA, Gretz N, Prinz M, Eils R, et al. Comparative transcriptome profiling of amyloid precursor protein family members in the adult cortex. BMC Genomics. 2011;12:160.
Bai Y, Markham K, Chen F, Weerasekera R, Watts J, Horne P, et al. The in vivo brain interactome of the amyloid precursor protein. Mol Cell Proteomics. 2008;7(1):15–34.
Bhattacharya SS, Wright AF, Clayton JF, Price WH, Phillips CI, McKeown CM, et al. Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28. Nature. 1984;309(5965):253–5.
Wright AF, Bhattacharya SS, Aldred MA, Jay M, Carothers AD, Thomas NS, et al. Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindred. J Med Genet. 1991;28(7):453–7.
Zhang H, Hanke-Gogokhia C, Jiang L, Li X, Wang P, Gerstner CD, et al. Mistrafficking of prenylated proteins causes retinitis pigmentosa 2. FASEB J. 2015;29(3):932–42.
Hua ZL, Emiliani FE, Nathans J. Rac1 plays an essential role in axon growth and guidance and in neuronal survival in the central and peripheral nervous systems. Neural Dev. 2015;10(1):21.
Haeseleer F, Sokal I, Gregory FD, Lee A. Protein phosphatase 2A dephosphorylates CaBP4 and regulates CaBP4 function. Invest Ophthalmol Vis Sci. 2013;54(2):1214–26.
Loosli F. ArhGEF18 regulated Rho signaling in vertebrate retina development. Small GTPases. 2013;4(4):242–6.
Neuillé M, Morgans CW, Cao Y, Orhan E, Michiels C, Sahel JA, et al. LRIT3 is essential to localize TRPM1 to the dendritic tips of depolarizing bipolar cells and may play a role in cone synapse formation. Eur J Neurosci. 2015;42(3):1966–75.
Pardue MT, McCall MA, LaVail MM, Gregg RG, Peachey NS. A naturally occurring mouse model of X-linked congenital stationary night blindness. Invest Ophthalmol Vis Sci. 1998;39(12):2443–9.
Pearring JN, Bojang Jr P, Shen Y, Koike C, Furukawa T, Nawy S, et al. A role for nyctalopin, a small leucine-rich repeat protein, in localizing the TRP melastatin 1 channel to retinal depolarizing bipolar cell dendrites. J Neurosci. 2011;31(27):10060–6.
Rao A, Dallman R, Henderson S, Chen CK. Gbeta5 is required for normal light responses and morphology of retinal ON-bipolar cells. J Neurosci. 2007;27(51):14199–204.
Cao Y, Masuho I, Okawa H, Xie K, Asami J, Kammermeier PJ, et al. Retina-specific GTPase accelerator RGS11/G beta 5S/R9AP is a constitutive heteotrimer selectively targeted to mGluR6 in ON-bipolar neurons. J Neurosci. 2009;29(29):9301–13.
Ishii M, Morigiwa K, Takao M, Nakanishi S, Fukuda Y, Mimura O, et al. Ectopic synaptic ribbons in dendrites of mouse retinal ON- and OFF-bipolar cells. Cell Tissue Res. 2009;338(3):355–75.
Tsukamoto Y, Omi N. Effects of mGluR6-deficiency on photoreceptor ribbon synapse formation: comparison of electron microscopic analysis of serial sections with random sections. Vis Neurosci. 2014;31(1):39–46.
Zheng H, Jiang M, Trumbauer ME, Sirinathsinghji DJ, Hopkins R, Smith DW, et al. beta-Amyloid precursor protein-deficient mice show reactive gliosis and decreased locomotor activity. Cell. 1995;81:525–31.
von Koch CS, Zheng H, Chen H, Trumbauer M, Thinakaran G, van der Ploeg LH, et al. Generation of APLP2 KO mice and early postnatal lethality in APLP2/APP double KO mice. Neurobiol. Aging. 1997;18:661–9.
Needham BE, Wlodek ME, Ciccotosto GD, Fam BC, Masters CL, Proietto J, et al. Identification of the Alzheimer's disease amyloid precursor protein (APP) and its homologue APLP2 as essential modulators of glucose and insulin homeostasis and growth. J. Pathol. 2008;215:155–63.
This work was supported by the National Health and Medical Research Council (NHMRC) to RC. Mohamed El Sanharawi is an employee of Eyevensys. We thank Prof. Hui Zheng (Baylor College of Medicine, Houston, TX, USA) for the APP knockout mice. We thank Prof. Sangram Sisodia (Department Of Neurobiology, The University of Chicago, IL, USA) for the APLP2 knockout mice. The authors would like to acknowledge Drs. Isabelle Audo and Christina Zeitz for the very stimulating discussion on the role of synaptic and development genes in CSNB.
Availability of data and materials
VD performed samples harvesting, morphological analysis, cell counting, immunochemistry, fluorescence microscopy, quantitative real-time PCR, statistical analysis, the data analysis as well as reviewed the data. VD also participated in the study design. GDC participated actively in the samples harvesting, reviewing the data and helped to draft and revise the manuscript. KD participated in tissue preparation, immunochemistry and electroretinogram. CB participated to tissue preparation and performed immunochemistry. IR-C performed electroretinogram, helped to draft the manuscript and participated in the revising the manuscript. CK oversaw some of the electroretinogram, participated in the data analysis and helped to draft the manuscript and participated in the revising the manuscript. MS participated in tissue preparation, performed transmission electron microscopy and helped to draft the manuscript. MES performed spectral domain optical coherence tomography, participated in morphological and some of the statistical analyzes and helped to draft the manuscript. LJ participated in tissue harvesting, also performed some of the immunochemistry and helped to transmission electron microscopy. CP and NA performed some of the immunochemistry. MA revised the manuscript. YA and FBC helped to the coordination and revised the manuscript. RC participated actively in the samples harvesting, reviewing the data and helped to draft and revise the manuscript. FM conceived of the study, and participated in its design, and coordination. FM helped to morphological analysis and cell counting, and drafted the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
All procedures involving mice conformed to the resolution on the use of animals in research of the Association for Research in Vision and Ophthalmology and to the guidelines of the Institut National de la Santé et de la RechercheMédicale Committee on Animal Research.
Virginie Dinet and Giuseppe D. Ciccotosto are co-first authors.
Roberto Cappai and Frédéric Mascarelli are co-senior authors.
Additional file 1: Figure S1.
APLP2 expression was localized in the two synaptic layers and overlapped extensively with APP in specific neuronal populations of the adult retina. Figure S2. The ultrastructure of the RPE in the adult retina did not differ between WT and APLP2-KO. Figure S3. Impaired retinal function at the level of the post-rod response in APLP2-KO. Figure S4. The ultrastructure of the ribbon photoreceptor presynaptic terminals differed dramatically between young WT and APLP2-KO. Figure S5. Deletion of APLP2 delays the development of the OPL. Figure S6. Perturbed retinal microglia cell activation and altered transcription of specific complement pathway in APLP2-KO. Table S1. Antibodies used for colabeling immunofluorescence experiments. Table S2. Loss of APLP2 does not alter gross lamination of young and adult retina. Table S3. APLP2 is required for the differentiation of bipolar and synaptogenesis of cone and rod terminals during postnatal development. Table S4. APLP2 is necessary for the generation of the ON and OFF pathways through the proper development of bipolar cell terminals during postnatal development. (DOC 4053 kb)
Rights and permissions
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
About this article
Cite this article
Dinet, V., Ciccotosto, G.D., Delaunay, K. et al. Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristics. Mol Brain 9, 64 (2016). https://doi.org/10.1186/s13041-016-0245-z
- Amyloid precursor protein
- Amyloid precursor-like protein 2
- Congenital stationary night blindness