Skip to main content

LAMP5 in presynaptic inhibitory terminals in the hindbrain and spinal cord: a role in startle response and auditory processing


Lysosome-associated membrane protein 5 (LAMP5) is a mammalian ortholog of the Caenorhabditis elegans protein, UNC-46, which functions as a sorting factor to localize the vesicular GABA transporter UNC-47 to synaptic vesicles. In the mouse forebrain, LAMP5 is expressed in a subpopulation of GABAergic neurons in the olfactory bulb and the striato-nigral system, where it is required for fine-tuning of GABAergic synaptic transmission. Here we focus on the prominent expression of LAMP5 in the brainstem and spinal cord and suggest a role for LAMP5 in these brain regions. LAMP5 was highly expressed in several brainstem nuclei involved with auditory processing including the cochlear nuclei, the superior olivary complex, nuclei of the lateral lemniscus and grey matter in the spinal cord. It was localized exclusively in inhibitory synaptic terminals, as has been reported in the forebrain. In the absence of LAMP5, localization of the vesicular inhibitory amino acid transporter (VIAAT) was unaltered in the lateral superior olive and the ventral cochlear nuclei, arguing against a conserved role for LAMP5 in trafficking VIAAT. Lamp5 knockout mice showed no overt behavioral abnormality but an increased startle response to auditory and tactile stimuli. In addition, LAMP5 deficiency led to a larger intensity-dependent increase of wave I, II and V peak amplitude of auditory brainstem response. Our results indicate that LAMP5 plays a pivotal role in sensorimotor processing in the brainstem and spinal cord.


Membrane trafficking is important for the generation of specialized cell structures and functions. In neurons, formation of polarized cell morphology requires long-distance transport of intracellular membrane organelles and membrane proteins to axons and dendrites [1,2,3,4,5,6]. In presynaptic boutons and postsynaptic dendritic spines, exocytotic and endocytotic membrane trafficking regulates efficacies of synaptic neurotransmission; e.g., regulation of neurotransmitter release probability by exocytosis of synaptic vesicles [7,8,9,10,11] and changes in the postsynaptic response by exo/endocytosis of neurotransmitter receptors [12,13,14]. In addition to ubiquitously expressed molecules that regulate general membrane trafficking, there are a variety of neuron-specific molecules that exert critical roles in neuronal structure and function [15, 16].

We recently developed a transcriptome database for various developmental stages of the mouse brain (BrainTx) and have identified several genes whose expression is brain specific and developmentally regulated [17, 18]. A gene encoding lysosome-associated membrane protein 5 (LAMP5) is one such gene that shows distinctive mRNA expression patterns during postnatal stages. Although LAMP5 belongs to the LAMP family based on structural similarity in the LAMP domain, it is different from other LAMP proteins in terms of tissue-specific expression. For example, LAMP5 is almost brain-specific, whereas LAMP1 and LAMP2 are expressed in cells of many tissues besides brain [19]. Moreover, in cortical pyramidal neurons, LAMP5 is mainly accumulated in distinct intracellular vesicles, which do not contain any known markers of classical intracellular transport pathways, and is not targeted to the late endosomal/lysosomal compartments [20] in which LAMP1 and LAMP2 are primarily localized. Thus, LAMP5 is expected to play a different role from that of LAMP1 and LAMP2 and to contribute to the unique function of the central nervous system (CNS); however, the distribution and function of the protein in the mammalian CNS is not well characterized.

A recent study investigated LAMP5 expression in the mouse forebrain and revealed that it is expressed in subpopulations of GABAergic neurons in the striato-nigral system and the olfactory bulb [21]. The protein is localized to synaptic terminals, where it overlaps with the vesicular GABA transporter or vesicular inhibitory amino acid transporter (VGAT/VIAAT), and deficiency of LAMP5 leads to altered pre-synaptic plasticity in striatopallidal synapses. Interestingly, UNC-46, a LAMP5 ortholog in Caenorhabditis elegans is also localized in the presynaptic terminals of all 26 GABAergic neurons [22]. It is essential for the axonal transport of VIAAT; the unc-46 mutant has disturbed GABA neurotransmission and motor coordination, suggesting a conserved role of LAMP5 as a VIAAT trafficking chaperon in the mammalian brain. However, LAMP5-deficiency in mice does not affect the subcellular localization of VIAAT in striatal neurons, posing the possibility that LAMP5 may be involved in GABA neurotransmission in a different manner in the mammalian brain [21].

There are many inhibitory neurons in the hindbrain and spinal cord of the mammalian CNS, but the expression and the subcellular localization of LAMP5 in these regions have not been reported. Therefore, in the present study, we addressed whether LAMP5 is localized in the inhibitory synaptic terminals and whether it is involved with the axonal transport of VIAAT in the brainstem and the spinal cord. We found a prominent expression of LAMP5 in these regions and, as in the forebrain, LAMP5 was localized in the synaptic terminals of the subpopulation of inhibitory neurons and was not essential for the proper localization of VIAAT in the brainstem. We further investigated the physiological function of LAMP5 by generating LAMP5-deficient mice. Interestingly, LAMP5 deficiency led to a remarkable increase in startle response and in auditory brainstem response especially at higher sound pressure level. Our results indicate a role of LAMP5 in senserimotor processing in the hindbrain and spinal cord.


Differential expression patterns of LAMP5 protein in the postnatal mouse CNS

We investigated the spatiotemporal expression profile of LAMP5 in the mouse CNS. We first analyzed 18 different regions of the adult mouse CNS, including the hindbrain regions and the spinal cord, and found that LAMP5 protein was expressed throughout the CNS with prominent expression in the pons, the medulla oblongata and the spinal cord (Fig. 1a). Moderate expression was observed in the inferior colliculus and the striatum, while expression was below the limit of detection in the cerebellum. LAMP5 expression was also observed in hypothalamus lysate; however, this was possibly because of incorporation of flanking regions, such as the ventral pallidum and the substantia nigra, because subsequent immunohistochemical analysis revealed that the flanking regions expressed LAMP5 strongly whereas the hypothalamus itself did not [21] (see below). Interestingly, the expression profile of Lamp5 mRNA was different from that of LAMP5 protein (lower panels in Fig. 1a). On one hand, a striking difference was observed in the cerebral cortex, where the transcript was highly expressed but the protein was barely detectable. On the other hand, the transcript was hardly detected in certain regions like the inferior colliculus and the hypothalamus where the protein was present, indicating that the protein was translated elsewhere and transported to the regions via axonal projections.

Fig. 1
figure 1

Spatiotemporal expression of LAMP5 protein in various brain regions. a Spatial distribution of LAMP5 protein and Lamp5 mRNA at P56. Total protein lysates and total RNA of indicated regions were subjected to western blotting (upper panel) and RT-PCR analyses (lower panel), respectively. Midbrain was the remaining of midbrain after the superior and inferior colliculi were removed. Amido black staining and Gapdh are shown as loading controls. b and c Developmental expression of LAMP5. LAMP5 expression in whole brains at P0, P3, P7, P14, P22 and P56 (b), and in the striatum, cerebellum, pons and medulla oblongata at P7, P14, P22 and P56 was analyzed (c)

We also analyzed LAMP5 expression during postnatal development at postnatal day 3 (P3), P7, P14, P22 and P56 in whole brain (Fig. 1b) and in several brain regions (Fig. 1c). Immunoblotting of whole brain samples revealed that LAMP5 expression increased drastically in the period between weaning and young adulthood (Fig. 1b). However, the expression levels of LAMP5 in each brain region showed regional specificity during development (Fig. 1c). In the striatum, the expression level of LAMP5 increased during postnatal development and reached a peak at P22 (juvenile stage). High expression was already detected at P7 in the pons and medulla, and reached a plateau at P14 that was maintained thereafter. In contrast, expression in cerebellar samples could not be detected at any postnatal stages. These results showed that LAMP5 is widely but specifically expressed in numerous brain regions during postnatal development with prominent expression in the hindbrain and spinal cord.

Restricted distribution of LAMP5 protein in the brain stem

Next, we investigated the distribution of LAMP5 in the adult brain and spinal cord by immunohistochemistry (Fig. 2). Consistent with the immunoblot results, strong immunoreactivity was observed in the pons and the medulla oblongata. The protein was also present in the ventral pallidum (VP) and the substantia nigra pars reticulata (SNr) as previously reported [21] (Fig. 2a).

Fig. 2
figure 2

LAMP5 immunoreactivity in the brain and spinal cord. A sagittal section of an adult mouse brain (a), and coronal sections of an adult brainstem (b) and spinal cord (c) were immunostained against LAMP5. DCO dorsal cochlear nucleus; M medulla oblongata; P pons, PnC Caudal pontine reticular formation, PSV principal sensory nucleus of the trigeminal, SOC superior olivary complex, SNr substantia nigra par reticulata, VCO ventral cochlear nucleus, vNLL ventral nucleus of lateral lemniscus, VP ventral pallidum. Scale bars: a, 1 mm; b, 300 μm; c, 300 μm

In coronal hindbrain sections LAMP5 was broadly distributed in the pons and the medulla oblongata with marked expression in the sensory-related nuclei of the pons and cochlear nuclei (Fig. 2b): namely, the ventral part of the nucleus of lateral lemniscus (vNLL), the principal sensory nucleus of the trigeminal nerve (PSV), the superior olivary complex (SOC) and the ventral and dorsal parts of the cochlear nucleus (VCO and DCO).

In the spinal cord, LAMP5 immunoreactivity was present throughout the dorsal, lateral and ventral horns of the gray matter and also in nerve fibers within the dorsal, lateral and ventral columns of the white matter (Fig. 2c). Similar distribution patterns were observed in the cervical, thoracic and lumber regions of the spinal cord.

LAMP5 is expressed in inhibitory projection neurons in the brainstem

Next, we examined whether LAMP5 was localized to inhibitory synaptic terminals in the hindbrain and the spinal cord. When we double-stained inhibitory axon termini with anti-LAMP5 and anti-VIAAT antibodies, the distributions of LAMP5 and VIAAT were highly similar in the hindbrain and spinal cord (Fig. 3a–b). For example, both VIAAT and LAMP5 showed a strong gradient across the lateral superior olive (LSO) with higher immunoreactivity in the lateral limb of this nucleus (lower panels in Fig. 3a). At a higher magnification, we found that LAMP5 was specifically co-localized with VIAAT and segregated from either vesicular glutamate transporter 1 (VGluT1)- or VGluT2-positive synaptic boutons (Fig. 3c). The co-localization of LAMP5 and VIAAT was also observed in the VCO, the vNLL, the PSV, the caudal pontine reticular formation (PnC) and the ventral and dorsal horn of the spinal cord (Fig. 3c–d and data not shown).

Fig. 3
figure 3

LAMP5 is localized in the inhibitory synaptic terminals. a LAMP5 and VIAAT expression in the adult brainstem. Lower panels: higher-magnification images of the superior olivary complex (SOC) at the positions indicated in the top images (rectangles with white dashed lines). Scale bars: upper, 500 μm; lower, 100 μm. b LAMP5 and VIAAT expression in the cervical spinal cord. Scale bars, 200 μm. c and d Confocal images of the lateral superior olive (LSO) and ventral cochlear nucleus (VCO) regions (c) and the ventral horn of the cervical spinal cord (d). LAMP5 was double-stained with VGluT1, VGluT2 or VIAAT. Scale bars, 5 μm. e Schematic diagram of the SOC nuclei. The medial nucleus of the trapezoid body (MNTB) neurons send inhibitory projection to the LSO, medial superior olive (MSO) and superior paraolivary nucleus (PSV) neurons. f Distribution of Lamp5-expressing neurons in the SOC. In situ hybridization data is from the Allen Mouse Brain Atlas (Experiment No. 70927827) [23]. g LAMP5 expression in MNTB neurons. The cell body of an MNTB neuron can be identified because excitatory synaptic terminals surround it. Right panel: Higher-magnification image of the MNTB neurons indicated by the white square in the left image. Scale bars: left, 25 μm; right, 10 μm

The LSO neurons receive major glycinergic input from principal neurons in the medial nucleus of the trapezoid body (MNTB) (Fig. 3e). According to the Allen Mouse Brain Atlas [23, 24], MNTB neurons express Lamp5 mRNA at a high level (Fig. 3f) but the MNTB itself did not show a strong immunoreactivity against LAMP5 (Fig. 3a, asterisk) and only weak immunoreactivity was detected in the cytoplasm of MNTB principal neurons (Fig. 3g). This suggests that LAMP5 expressed in MNTB neurons was transported to their synaptic terminals located in the LSO.

Generation of a Lamp5-deficient mouse

To reveal molecular and physiological functions of LAMP5, we generated a Lamp5 mutant mouse line using the CRISPR/Cas9 system. We used three guide RNAs targeting either exon 2 or the 3′ splice site of intron 5 of the Lamp5 gene and obtained a mutant mouse carrying a deletion spanning from the middle of exon 2 to the 3′ end of intron 5 with a 3-base insertion (Fig. 4a and b). The mutation resulted in the in-frame fusion of the 5′ half of exon 2 and the last exon, and the loss of most of the LAMP5 protein other than the signal peptide. Thus the polypeptide encoded by the mutant allele is predicted to be non-functional (Fig. 4c). The absence of the full-length LAMP5 protein was confirmed by western blotting of whole brain lysates from wild type, and heterozygous and homozygous Lamp5 mutants (Fig. 4d). Hereafter, we call the homozygous mutant Lamp5 KO.

Fig. 4
figure 4

Generation of a Lamp5 KO mouse. a Schematic diagram of the wild-type (WT) and Lamp5 KO alleles. Arrows, CRISPR/Cas9 target sites; gray box, untranslated region; black box, coding region; solid line, intron; dashed line, deleted region in the KO allele. Exon 2 is fused with exon 6. b DNA sequences of the WT and KO alleles. The mutated sequence is shown in red. A termination codon appears at the beginning of exon 6 (underlined). c Amino acid sequences of proteins encoded by the WT and KO alleles. The epitope used for primary antibody production is underlined. d LAMP5 protein expression in whole brain lysates of WT (+/+), heterozygous and homozygous Lamp5 KO (+/− and −/−) mice. β-actin served as a loading control

Involvement of LAMP5 in axonal transport of VIAAT

Using Lamp5 KO mice, we examined whether LAMP5 was involved with the axonal transport of VIAAT. LAMP5-expressing MNTB neurons provide major glycinergic input to the LSO neurons; therefore, we investigated VIAAT expression in the LSO. The immunoreactivity for VIAAT and the ratio of VIAAT to VGluT2 were not altered in KO animals (Fig. 5a–b, and data not shown). We also investigated the VCO and failed to detect any change in VIAAT expression in Lamp5 KO mice (Fig. 5c–d). These results indicate that LAMP5 is not essential for the axonal transport of VIAAT in these nuclei.

Fig. 5
figure 5

VIAAT and VGluT2 in the LSO and VCO in Lamp5 KO mice. a VIAAT and VGluT2 immuoreactivities in the LSO of WT and KO sections. b Quantitative analysis of VIAAT and VGluT2 immunoreactivities in the LSO (indicated by dashed lines in a). c VIAAT and VGluT2 immuoreactivities in the VCO. d Quantitative analysis of VIAAT and VGluT2 immunoreactivities in the VCO (indicated by dashed lines in c). Two-tailed Welch’s t-test revealed no significant difference between the genotypes, either in the LSO or VCO (p > 0.05, n = 4 mice for each genotype). Error bars represent SEM

Exaggerated startle response in Lamp5 KO mice

Next, we performed a series of behavioral tests including tests that evaluate brainstem- and spinal cord-related functions. Open field, elevated plus maze and rotarod tests showed that Lamp5 KO mice have no overt abnormalities in locomotor activity, anxiety-related behavior, motor coordination and motor learning (Fig. 6a–c). Interestingly, however, we found that Lamp5 KO mice showed increased startle response to unexpected loud noise (Fig. 6d). The mutants also showed decreased prepulse inhibition (PPI) of the acoustic startle reflex (Fig. 6e), indicating that LAMP5 deficiency led to abnormal sensorimotor processing. Because LAMP5 was expressed in the inhibitory synaptic terminals in the cochlear nuclei, the SOC and the vNLL, all of which are involved with auditory processing, we assumed that the increased startle reflex in Lamp5 KO mice might result from increased excitability of the brainstem auditory circuit. We therefore analyzed auditory brainstem response (ABR) to tone-burst stimuli at various frequencies (4, 8, 16 and 31.25 kHz) (Fig. 7). ABR threshold was not different between the genotypes (Fig. 7b), but the amplitude of ABR appeared to be larger in KO animals (Fig. 7a). When we analyzed the peak amplitude of ABR waves at 16 kHz, wave I, II and V were significantly larger especially at the higher sound pressure level. Meanwhile, a tactile stimulus also elicited an increased startle response in the KO mice (Fig. 6f), indicating that there was no stimulus specificity in the exaggeration of the startle response in KO mice. Taken together, knockout of the Lamp5 gene led to an increased startle response and smaller PPI as well as an increased ABR, indicating that LAMP5 plays an essential role in regulating brainstem- and spinal cord-mediated sensorimotor and auditory processing ability. These findings are consistent with the immunohistochemistry findings.

Fig. 6
figure 6

Behavioral analysis of Lamp5 KO mice. a Open field test. There was no significant difference between genotypes in the total distance travelled or in the time spent in the outer or inner zones (two-tailed Welch’s t-test, n = 8 mice for each genotype). b Elevated plus maze test. There was no significant difference between genotypes in time spent in the open arm or the closed arm (two-tailed Welch’s t-test, n = 8 mice for each genotype). c Rotarod test. Two-way repeated-measures ANOVA (genotype × time) revealed a significant main effect of time (F(3,42) = 9.458, p < 0.0001), a non significant effect of genotype (F(1,15) = 2.51, p > 0.05) and a non significant interaction between factors (F(3,42) = 0.1307, p = 0.9413). Body weight after the fourth trial was not different between genotypes (two-tailed Welch’s t-test, n = 8 mice for each genotype). d Startle response to 120 dB white noise stimuli. The response was larger in KO mice (p < 0.05, Two-tailed Welch’s t-test, n = 5 mice for each genotype). e Percent inhibition of auditory startle response by prepulse stimulation. Two-way repeated-measures ANOVA (genotype × prepulse) revealed a significant effect of prepulse intensity (F(3,32) = 23.0, p < 10− 7) and of genotype (F(1,32) = 13.2, p < 0.001) but no significant interaction between factors (F(3,32) = 2.90, p > 0.05). f Startle response to air-puff stimuli. The response was larger in KO mice (p < 0.05, Two-tailed Welch’s t-test, n = 8 mice for each genotype). * p < 0.05, *** p < 0.001. Error bars indicate SEM

Fig. 7
figure 7

Auditory brainstem response (ABR) of Lamp5 KO mice. a Representative ABR waveform to 12 kHz tone-burst stimuli recorded from wild type and a Lamp5 KO. b ABR threshold. Two-way repeated-measures ANOVA (genotype × frequency) revealed a significant main effect of frequency (F(3,36) = 57.68, p < 0.0001), a non significant effect of genotype (F(1,12) = 0.0124, p = 0.9133) and a significant interaction between factors (F(3,36) = 2.921, p = 0.0471). Post-hoc Welch’s t-test revealed no significant difference between genotypes at either frequency (n = 7 for each genotype). c Amplitude of ABR waves at 16 kHz. The waves were indicated in a. Two-way repeated-measures ANOVA (genotype × sound intensity) and post-hoc Welch’s t-test were performed for each wave. A significant main effect of genotype and a significant interaction between factors were present in wave I (F(1,12) = 10.15, p = 0.0078; F(3,36) = 2.301, p = 0.0936, respectively), wave II (F(1,12) = 8.977, p = 0.0111; F(3,36) = 4.062, p = 0.0139, respectively) and wave V (F(1,12) = 16.19, p = 0.0017; F(3,36) = 5.341, p = 0.0038, respectively). * p < 0.05, ** p < 0.01, *** p < 0.001. Error bars indicate SEM


In the present study, we characterized the spatial and temporal distribution of LAMP5 in the mouse hindbrain and spinal cord. We found that LAMP5 was expressed in the pons and medulla oblongata at relatively high levels by P7. According to the Allen Developing Mouse Brain Atlas [25], expression of Lamp5 mRNA can be observed in the hindbrain and spinal cord as early as at embryonic day 11.5 (E11.5) and then spreads to the midbrain and forebrain regions after birth [23], as also shown in this study. In the spinal cord, synaptic contact occurs on motor neurons at E11.5 and the first synaptic activity can be recorded the following day [26,27,28,29,30], whereas synaptogenesis occurs postnatally in the forebrain and peaks in the juvenile stage [31]. Thus, the temporal transition of LAMP5 expression was consistent with the synaptic formation in the striatum, pons and medulla.

Our immunohistochamical analysis showed that LAMP5 was localized exclusively in inhibitory synaptic terminals in the pons and spinal cord, suggesting its role in inhibitory neurotransmission. Two studies have reported that LAMP5 and its ortholog function in GABAergic nerve terminals [21, 22]. One showed that in C. elegans, the LAMP5 ortholog, UNC-46, is expressed in every GABAergic motor neuron and acts as a sorting chaperone that localizes VIAAT to synaptic terminals [22]. In unc-46 mutants, frequency of miniature currents is severely reduced possibly due to a reduced number of vesicles that harbored the transporter. The other study showed that in mammals, LAMP5 is localized in inhibitory synaptic terminals of granule cells of the olfactory bulb and in striatal neurons [21]; however, the study also showed that LAMP5 is not essential for correct localization of VIAAT in these neurons, arguing against the conserved role of axonal trafficking of the transporter. In the present study, we showed that VIAAT immunoreactivity was not altered in the LSO or VCO of LAMP5-deficient mice, indicating that LAMP5 has little to do with terminal localization of VIAAT in the brainstem. Nevertheless, LAMP5-deficiency has a complex impact on the striatopallidal synapse function: the frequency of activity-independent currents is increased while the evoked release probability is decreased as indicated by a strong paired-pulse facilitation of inhibitory postsynaptic currents [21]. Although it is yet unknown how LAMP5 affects presynaptic release machinery, the study suggested the importance of LAMP5 on fine-tuning of GABAergic neurotransmission. We speculate that LAMP5 achieves its function by regulating turnover of some membrane proteins or vesicles, because a study of cortical neurons that showed LAMP5 was subjected to endocytosis and localized in uncharacterized early endocytic organelles [20]. Taken together, these results suggest that LAMP5-deficiency can lead to a compromised neurotransmission of inhibitory synapses in the hindbrain and spinal cord.

LAMP5 deficiency did not cause any overt behavioral abnormality but specifically led to increased startle responses to both auditory and tactile stimuli. Interestingly, dysfunction of glycinergic neurotransmission, which is a major source of synaptic inhibition in the hindbrain and spinal cord, is known to cause exaggerated startle response. For example, the mouse mutant spasmodic, which carries a mutation in the gene encoding the glycine receptor subunit alpha 1 (Glra1) that decreases its ligand binding affinity, presents massive tremor and exaggerated startle response to sound and touch three weeks after birth [32,33,34]. Similar phenotypes are caused by mutations in genes encoding glycine receptor subunit beta (Glrb) [35, 36], glycine transporter 2 (Slc6a5) [37] or gephyrin [38], which is required in glycine receptor clustering [39]. Therefore, one possible explanation of the increased startle response is that LAMP5 deficiency led to dysfunctional glycinergic neurotransmission in the brainstem and spinal cord. Auditory and tactile stimuli are conveyed via the auditory and trigeminal sensory pathway, respectively, to giant neurons in the PnC. The neurons send direct projections to motor neurons that innervate facial and skeletal muscles and elicit movement of startle reflex. LAMP5 can potentially affect startle response either upstream or downstream from the PnC because the protein was expressed both in nuclei composing the auditory and trigeminal pathways (e.g., VCO and PSV) and in the ventral horn of spinal cord where somata of motor neurons exist. The startle response can also be potentiated by fear and anxiety [40]; however, because our behavioral analysis showed that LAMP5 deficiency did not affect emotional behavior, and a study from another group showed that it even decreases anxiety [21], it is unlikely that the startle response was potentiated by the animals’ anxious state.

The normal ABR threshold of LAMP5-deficient mice indicates that function of the cochlear hair cell is conserved. However, the mutant mice showed a larger increase in peak amplitude of waves I, II and V than wild type controls as the sound pressure level of auditory stimuli increased. The larger amplitude of wave I indicates auditory input evokes greater neuronal activity already at the cochlear spiral ganglion. The function and expression of LAMP5 in the cochlea has yet to be shown, but the protein can possibly regulate the cochlear output via SOC neurons because the SOC gives rise to the olivocochlear system that is involved with a descending control of the cochlea [41]. Especially, the medial olivocochlear system (MOCS) is a strong candidate that may lead the altered ABR in Lamp5 KO animals. Several studies demonstrated that electrical stimulation of the MOCS decreases activity of the auditory nerve by inhibiting the active mechanical amplification process of the outer hair cells [42,43,44,45]. The MOCS activity depends on sound pressure level of input [46]; therefore, a compromised function of the MOCS will increase auditory nerve responses especially when a loud auditory stimulus is applied. Because the input/output function of ABR waves was increased in Lamp5 KO mice, we assume that LAMP5 deficiency brings about functional deficits in the MOCS thereby enhancing neural activity of the cochlear nerve at higher intensity of sound input. The MOCS stems from large multipolar neurons that reside in the ventral nucleus of the trapezoid body (VNTB), where neurons highly express Lamp5 mRNA according to Allen Mouse Brain Atlas. Thus it is likely that LAMP5 functions in the MOCS. Thus elevated response to auditory stimuli is considered to contribute at least in part to the potentiated auditory startle response.

The present study showed LAMP5 to be expressed widely in the inhibitory synaptic terminals of the pons, medulla oblongata and spinal cord and indicates a role in the acoustic and tactile startle reflex. Our results exclude the possibility that the exaggerated startle response in Lamp5-deficient mice was caused by decreased axonal trafficking of VIAAT. Further studies will elucidate the detailed physiological properties of LAMP5 in this reflex pathway.



C57BL/6J mice were purchased from CLEA Japan, Tokyo, Japan. Recipient ICR mice were purchased from Charles River Laboratories JAPAN, Kanagawa, Japan. All animals were treated according to the recommendations and protocols approved by the Animal Care and Use Committee of Tokyo University of Science and by the Animal Welfare Committee of the University of Tokyo. Animals were housed in an environment with a 12-h/12-h light/dark cycle (daytime 8:00–20:00) with controlled temperature (23 ± 2 °C) and humidity (55 ± 10%) and ad libitum access to food and water.

Cas9 mRNA and sgRNA preparation

A plasmid template for in vitro transcription of Cas9 mRNA was kindly provided by Dr. T. Mashimo (Kyoto University). The plasmid encodes a Cas9 protein flanked by SV40 nuclear localization signals with a 90-bp poly(A) tail in the 3′-untranslated region, which facilitates its translation in zygotes [47]. Cas9 mRNA was transcribed using a MessageMAX T7 ARCA-Capped Message Transcription Kit (CELLSCRIPT, Madison, WI, USA), polyadenylated with an A-Plus Poly(A) Polymerase Tailing Kit (CELL SCRIPT) and purified using a MEGAclear Kit (Life Technologies). Three single guide RNAs (sgRNAs) were designed to target either exon 2 or 6 of the Lamp5 gene (Fig. 4). Their protospacer sequences with PAM (underlined) were as follows: CTTTCTCGGGGTTCGTGGAAAGG, AAATGGGACGACGTGTCTCATGG and GCGATGTACTTATTAACTGCGGG. These protospacers were cloned into BsaI-digested pDR274 vector (Addgene ID #42250) and the resulting plasmids served as templates for in vitro transcription. The sgRNAs were transcribed using a MEGAshortscript T7 Transcription Kit (Thermo Fisher Scientific K.K., Tokyo, Japan) and purified using a mini Quick Spin Column (Roche Diagnostics K.K., Tokyo, Japan). All procedures were performed according to the manufacturers’ instructions.

Embryo collection and electroporation

Cas9 mRNA and sgRNA were delivered by electroporation to C57BL/6J embryos at the pronuclear stage as described previously with slight modifications [48]. Briefly, the embryos were washed three times with Opti-MEM I (Thermo Fisher Scientific) supplemented with 0.1% polyvinylalchol (PVA) and once with 0.1% PVA-Opti MEM I containing Cas9 mRNA (400 ng/μl) and the three sgRNAs (100 ng/μl each). Then the embryos ware placed in a line in the gap of an electrode (LF501PT1–10, BEX, Tokyo, Japan) filled with RNA-containing 0.1% PVA-Opti-MEM I (total 5 μl in volume) and electroporation was performed using a CUY21EDIT II electroporator (BEX). After electroporation, the embryos were immediately collected from the electrode chamber and transferred into oviducts of 0.5-day-post-coitum recipients.

Generation and genotyping and of Lamp5 KO mice

Genomic DNA was extracted from mouse tail biopsies to serve as templates for genotyping PCR. The PCR primers for the Lamp5 locus were as follows: Fw, AATATGAGTTTGGTGGCGGT; Rv, TCATTGCATTCGCTCGGTAA. The genotypes of the founder generation were determined by sequencing the amplified PCR fragment directly. One allele of a founder male had a deletion spanning from exon 2 to 6 (Fig. 4a-b), which resulted in truncation of most of the encoded polypeptide (Fig. 4c). This male was mated with C57BL/6J females to obtain F1 mice. For biochemical and behavioral analyses, we used F2 and F3 generation of the mice.


An anti-LAMP5 polyclonal antibody was raised in rabbit against the peptide “QVQIPRDRSQYKHM”, corresponding to the cytoplasmic tail of LAMP5 (Fig. 4c). We confirmed the specificity of the antibody to LAMP5 by immunoblotting and immunohistochemistry with Lamp5 KO samples (Fig. 4d and Additional file 1). An anti-LAMP5 guinea pig polyclonal antibody (#412005) was purchased from Synaptic Systems (Goettingen, Germany). This antibody was used only for co-immunostaining of brainstem and spinal cord slices (Fig. 3). An anti-β-actin (#A2228) mouse monoclonal antibody was purchased from Sigma-Aldrich Japan (Tokyo, Japan). An anti-VGAT/VIAAT mouse monoclonal antibody (#131011) was purchased from Synaptic Systems. An anti-VGAT/VIAAT guinea pig polyclonal antibody, and anti-VGluT1 and anti-VGluT2 goat polyclonal antibodies were kindly provided by Dr. Masahiko Watanabe (Hokkaido University). Horseradish peroxidase (HRP)-conjugated anti-rabbit IgG (H + L) (#474–1506) secondary antibody was purchased from KPL (Gaithersburg, MD, USA), and HRP-conjugated anti-rabbit IgG (H + L) (#711–035-152) and anti-mouse IgG (H + L) (#715–035-152) secondary antibodies were from Jackson ImmunoResearch (West Grove, PA, USA). Alexa Fluor 488-labeled donkey anti-rabbit IgG (H + L) (#A21206), goat anti-guinea pig IgG (H + L) (#A11073) and donkey anti-goat IgG (H + L) (#705–035-003) secondary antibodies were purchased from Thermo Fisher Scientific. Cy3-labeled donkey anti-guinea pig IgG (H + L) (#706–165-148) and Cy5-labeled donkey anti-mouse IgG (H + L) (#715–175-151) secondary antibodies were purchased from Jackson ImmunoResearch.

Western blotting

To analyze LAMP5 expression in brains and spinal cords, brains were dissected from male mice and homogenized using a motor-driven glass Teflon homogenizer in RIPA buffer [50 mM Tris-HCl (pH 8.0), 150 mM NaCl, 1% Triton X-100, 0.5% sodium deoxycholate and 0.1% SDS] supplemented with cOmplete ULTRA (Sigma Aldrich). The homogenate was centrifuged at 13,000×g for 20 min with a tabletop centrifuge. The supernatant was used for further analysis. All protein samples were electrophoretically resolved in 8% gels by SDS-PAGE and electroblotted onto Immobilon-P PVDF membranes (Merck, Darmstadt, Germany). If not otherwise specified, 10 μg of proteins was loaded to each lane. The blots were processed at room temperature by immersion for 1 h in blocking buffer consisting of 5% (w/v) skimmed milk (Megmilk Snow Brand, Sapporo, Japan) in 1× TBS containing 0.1% (v/v) Tween 20 (TBST), then exposing them to primary antibody in blocking buffer for 1 h, washing them with TBST and, finally, exposing them to HRP-conjugated secondary antibody in blocking buffer for 1 h. After washing with TBST, bound antibody was detected using Immobilon Western Chemiluminescent HRP substrate (Merck) or ECL Prime (GE Healthcare Japan, Tokyo, Japan). Images were obtained using ImageQuant LAS 4000 mini (GE Healthcare Japan).

Reverse transcription PCR

Total RNA was extracted from freshly frozen brain tissues using an RNeasy Mini Kit (QIAGEN, Tokyo, Japan) and reverse transcribed using a PrimeScirpt RT-PCR Kit (Takara Bio, Shiga, Japan) with oligo dT primer. cDNA was amplified with Ex Taq (Takara Bio). The sequences of the primers used in RT-PCR for Lamp5 and Gapdh were as follows: Lamp5-Fw, TCACCATGATCCTGTCCGCA; Lamp5-Rv, CCCATGTGCTTGTACTGGGAA; Gapdh-Fw, CCGTGTTCCTACCCCCAATGTGTCC; Gapdh-Rv, GCCATGTAGGCCATGAGGTCCACCAC. For semi-quantitative analysis, the number of thermal cycles was determined so that the amplification was not saturated. PCR products were electrophoretically resolved on 1% agarose gels and stained with ethidium bromide.


Forty-micrometer-thick sagittal sections of male mouse brains were rinsed once with PBS and immersed in blocking buffer [1 × PBS containing 0.2% (v/v) Triton X-100 and 2–5% (v/v) donkey serum (D9663, Sigma-Aldrich)] for 30 min before incubation with primary antibody in blocking buffer for 2 h or overnight at room temperature. The sections were then washed three times with PBS and incubated with secondary antibody for 2 h at room temperature. After three washes with PBS, the sections were mounted using VECTASHIELD Mounting Medium (Vector Laboratories, Burlingame, CA, USA). Images were obtained using a fluorescence microscope (BZ-8000, KEYENCE, Osaka, Japan) and a confocal laser microscope (SP5, Leica microsystems, Wetzlar, Germany). For quantitative analysis of immunoreactivity, images were obtained using a confocal microscope with the pinhole open to be the maximum and were processed using Image J software (v.1.51) [49]. Regions of interest (ROIs) were drawn manually by visual inspection. A rectangular ROI was also chosen in an area where a specimen was not present to serve as a background. Background-subtracted mean gray values for each mouse were pooled and averaged across mice of each genotype. At least three sections per mouse were used.

Behavioral tests

Lamp5 KO males and littermate control males were subjected to behavioral tests. Cohort A (n = 8 for each genotype) was subjected to open field, elevated plus maze, rotarod and tactile startle response tests in this order at 12 weeks of age. Cohort B (n = 5 for each genotype) was subjected to auditory startle response and prepulse inhibition (PPI) tests at 13 weeks of age. All mice were habituated to the testing room for at least 1 h before each experiment.

Open field test

Mice were placed in the center of the open field (75 cm diameter) and allowed to explore freely the arena for 5 min under bright light conditions (600 lx). Their movement was recorded via a camera mounted above the arena, and their activity was measured automatically using Smart 3.0 video tracking software (Panlab, Barcelona, Spain). The open field was divided into an inner circle (50 cm diameter), and an outer area surrounding the inner circle. Measurements included total distance traveled and time spent in the inner and outer sections. The open field arena was cleaned with 70% ethanol and wiped with paper towels between each trial.

Elevated plus maze test

The elevated plus-maze consisted of two open arms (29.5 cm long × 6 cm wide), two closed arms surrounded by wall (15 cm high) and a central platform (6 cm × 6 cm) halfway between all arms. The entire apparatus was elevated to height of 55 cm above floor level. Mice were placed in the central platform facing an open arm and allowed to move freely through the maze for 10 min under moderate light conditions (25 lx). Their behavior was recorded via a camera mounted above the apparatus. Time spent in the open and closed arms was measured. The maze was cleaned with 70% ethanol and wiped with paper towels between each trial.

Rotarod test

The rotarod (Muromachi Kikai, Tokyo, Japan) consisted of a gritted metal roller (3 cm in diameter). A mouse was placed on the rotating roller and the time it remained on the roller was measured. The rotation speed of the roller was initially 4 rpm and increased linearly to 40 rpm over 300 s. One trial was carried out per day and the test was conducted for four consecutive days.

Startle response test and PPI test

The startle response was measured using an SR-Lab system (San Diego Instruments, San Diego, CA, USA). A mouse was placed in a small/medium animal enclosure (12.7 cm, 3.8 cm inner diameter) under moderately bright light conditions (260 lx) and was allowed to acclimate for 10 min. The movement of the animal in the startle chamber was measured by a piezoelectric accelerometer mounted under the enclosure at the sampling rate of 1 kHz. For the tactile startle response test, animals were subjected to 20 startle trials and five no-stimulus trials. In each startle trial, animals received an air-puff at the pressure of 0.1 MPa from a tube installed through a hole on the top of the enclosure. The puff of air lasted 100 msec. During the session, including the acclimation period, background white noise of 73 dB was continually present to reduce responses induced by noise from the air tubing. For the auditory startle response and PPI test, the animal then received 20 startle trials, 10 no-stimulus trials and 40 PPI trials. The inter-trial intervals were between 10 and 20 s and the total session lasted 17 min. The startle trial consisted of a single 120 dB white noise burst lasting 40 ms. The PPI trial consisted of a prepulse (20 ms burst of white noise at 69, 73, 77 or 81 dB intensity) followed, 100 ms later, by the startle stimulus (120 dB, 40 ms white noise). Each of the four prepulse trials (69, 73, 77 or 81 dB) was presented 10 times. Five consecutive startle trials were presented at the beginning and end of the session. The remainder of sixty different trials was presented pseudorandomly, ensuring that each trial was presented 10 times and that no two consecutive trials were identical. During the session, including the acclimation period, background white noise of 65 dB was continually present. The recording started 20 ms after startle stimulus onset and lasted for 60 ms. The largest amplitude in the recording window was taken as the startle amplitude for the trial. Basal startle amplitude was determined as the mean startle amplitude of the 20 startle trials. PPI (%) was calculated as follows: 100 × (pulse-alone response – prepulse-pulse response)/pulse-alone response, in which the prepulse-pulse response was the mean of the 10 PPI trials (69, 73, 77 or 81 dB) and the pulse-alone response was the basal startle amplitude.

Auditory brainstem response

ABR was recorded from mouse cohort A after the series of behavioral analyses as described previously [50]. Briefly, mice were anesthetized with ketamine hydrochloride (50 mg/kg, i.p.) and xylazine hydrochloride (10 mg/kg, i.p.). Before the ABR measurements, the external auditory canals and tympanic membranes were confirmed to be normal in all mice. Subdermal needle electrodes were placed on the vertex (active electrode), in the postauricular area of the measured ear (reference electrode), and in the postauricular area of the opposite ear (ground electrode). ABRs were evoked with tone-bursts (5 ms duration at 4, 8, 16, and 31.25 kHz) and measured by a recording system (Neuropack Ʃ MEB2208, Nihon Kohden). A speaker was placed 10 cm from the tragus of the stimulated ear. ABRs from 500 trials were averaged at each sound intensity. ABR thresholds were estimated by changing the intensity in 5 bB steps and finding the lowest sound intensity where reliable response peaks were detected. Peak amplitudes of ABR waves I, II and V were defined as follows: wave I, height from the baseline (0 ms); wave II, height from the subsequent trough; wave V, height from the previous trough.



Auditory brainstem response


Central nervous system


Clustered regularly interspaced short palindromic repeat


Dorsal parts of the cochlear nucleus


Deoxyribonucleic acid


Embryonic day


Gamma-Aminobutyric acid


Glyceraldehyde-3-phosphate dehydrogenase


Horse raddish peroxidse


Knock out


Lysosome-associated membrane protein


Lateral superior olive


Medial nucleus of the trapezoid body


Medial olivocochlear system


Messenger ribonucleic acid


Medial superior olive


Postnatal day


Polyacrylamide gel electrophoresis


Protospacer adjacent motif


Phosphate-buffered saline


Polymerase chain reaction


Caudal pontine reticular formation


Prepulse inhibition


Principal sensory nucleus of the trigeminal




Posteroventral cochlear nucleus


Polyvinylidene difluoride


Ribonucleic acid


Region of interest


Reverse transcription


Sodium dodecyl sulfate


Single guide ribonucleic acid


Substantia nigra par reticulata


Superior olivary complex


Superior paraolivary nucleus


Tris-buffered saline


Ventral parts of the cochlear nucleus


Vesicular GABA transporter


Vesicular glutamate transporter


Vesicular inhibitory amino acid transporter


Ventral part of the nucleus of lateral lemniscus


Ventral nucleus of the trapezoid body


Ventral pallidum


wild type


  1. Nishimura T, Kato K, Yamaguchi T, Fukata Y, Ohno S, Kaibuchi K. Role of the PAR-3–KIF3 complex in the establishment of neuronal polarity. Nat Cell Biol. 2004;6(4):328–34.

    CAS  PubMed  Google Scholar 

  2. Horiguchi K, Hanada T, Fukui Y, Chishti AH. Transport of PIP3 by GAKIN, a kinesin-3 family protein, regulates neuronal cell polarity. J Cell Biol. 2006;174(3):425–36.

    CAS  PubMed  PubMed Central  Google Scholar 

  3. Kapitein LC, Hoogenraad CC. Which way to go? Cytoskeletal organization and polarized transport in neurons. Mol Cell Neurosci. 2011;46(1):9–20.

    CAS  PubMed  Google Scholar 

  4. Wang T, Liu Y, Xu XH, Deng CY, Wu KY, Zhu J, et al. Lgl1 activation of Rab10 promotes axonal membrane trafficking underlying neuronal polarization. Dev Cell. 2011;21(3):431–44.

    CAS  PubMed  Google Scholar 

  5. Lalli G. RalA and the exocyst complex influence neuronal polarity through PAR-3 and aPKC. J Cell Sci. 2009;122(10):1499–506.

    CAS  PubMed  Google Scholar 

  6. Lalli G. Regulation of neuronal polarity. Exp Cell Res. 2014;328(2):267–75.

    CAS  PubMed  Google Scholar 

  7. Jahn R, Fasshauer D. Molecular machines governing exocytosis of synaptic vesicles. Nature. 2012;490(7419):201–7.

    CAS  PubMed  PubMed Central  Google Scholar 

  8. Sadakata T, Shinoda Y, Sekine Y, Saruta C, Itakura M, Takahashi M, et al. Interaction of calcium-dependent activator protein for secretion 1 (CAPS1) with the class II ADP-ribosylation factor small GTPases is required for dense-core vesicle trafficking in the trans-Golgi network. J Biol Chem. 2010;285(49):38710–9.

    CAS  PubMed  PubMed Central  Google Scholar 

  9. Sadakata T, Sekine Y, Oka M, Itakura M, Takahashi M, Furuichi T. Calcium-dependent activator protein for secretion 2 interacts with the class II ARF small GTPases and regulates dense-core vesicle trafficking. FEBS J. 2012;279(3):384–94.

    CAS  PubMed  Google Scholar 

  10. Sadakata T, Kakegawa W, Shinoda Y, Hosono M, Katoh-Semba R, Sekine Y, et al. CAPS1 deficiency perturbs dense-Core vesicle trafficking and Golgi structure and reduces presynaptic release probability in the mouse brain. J Neurosci. 2013;33(44):17326–34.

    CAS  PubMed  Google Scholar 

  11. Shinoda Y, Ishii C, Fukazawa Y, Sadakata T, Ishii Y, Sano Y, et al. CAPS1 stabilizes the state of readily releasable synaptic vesicles to fusion competence at CA3-CA1 synapses in adult hippocampus. Sci Rep. 2016;6:31540.

    CAS  PubMed  PubMed Central  Google Scholar 

  12. Anggono V, Huganir RL. Regulation of AMPA receptor trafficking and synaptic plasticity. Curr Opin Neurobiol. 2012;22(3):461–9.

    CAS  PubMed  PubMed Central  Google Scholar 

  13. Kakegawa W, Katoh A, Narumi S, Miura E, Motohashi J, Takahashi A, et al. Optogenetic control of synaptic AMPA receptor endocytosis reveals roles of LTD in motor learning. Neuron. 2018;99(5):985–98.

    CAS  PubMed  Google Scholar 

  14. Malinow R, Malenka RC. AMPA receptor trafficking and synaptic plasticity. Annu Rev Neurosci. 2002;25:103–26.

    CAS  PubMed  Google Scholar 

  15. Jahn R, Scheller RH. SNAREs — engines for membrane fusion. Nat Rev Mol Cell Biol. 2006;7(9):631–43.

    CAS  PubMed  Google Scholar 

  16. D'Adamo P, Masetti M, Bianchi V, More L, Mignogna ML, Giannandrea M, et al. RAB GTPases and RAB-interacting proteins and their role in the control of cognitive functions. Neurosci Biobehav Rev. 2014;46:302–14.

    CAS  PubMed  Google Scholar 

  17. Sato A, Sekine Y, Saruta C, Nishibe H, Morita N, Sato Y, et al. Cerebellar development transcriptome database (CDT-DB): profiling of spatio-temporal gene expression during the postnatal development of mouse cerebellum. Neural Netw. 2008;21(8):1056–69.

    PubMed  Google Scholar 

  18. The Brain Transcriptome Database. Accessed 10 Apr 2014.

  19. Wilke S, Krausze J, Buessow K. Crystal structure of the conserved domain of the DC lysosomal associated membrane protein: implications for the lysosomal glycocalyx. BMC Biol. 2012;10:62.

    CAS  PubMed  PubMed Central  Google Scholar 

  20. David A, Tiveron M-C, Defays A, Beclin C, Camosseto V, Gatti E, et al. BAD-LAMP defines a subset of early endocytic organelles in subpopulations of cortical projection neurons. J Cell Sci. 2007;120(2):353–65.

    CAS  PubMed  Google Scholar 

  21. Tiveron M-C, Beurrier C, Ceni C, Andriambao N, Combes A, Koehl M, et al. LAMP5 fine-tunes GABAergic synaptic transmission in defined circuits of the mouse brain. PLoS One. 2016;11(6):e0157052.

    PubMed  PubMed Central  Google Scholar 

  22. Schuske K, Palfreyman MT, Watanabe S, Jorgensen EM. UNC-46 is required for trafficking of the vesicular GABA transporter. Nat Neurosci. 2007;10(7):846–53.

    CAS  PubMed  Google Scholar 

  23. Lein ES, Hawrylycz MJ, Ao N, Ayres M, Bensinger A, Bernard A, et al. Genome-wide atlas of gene expression in the adult mouse brain. Nature. 2007;445(7124):168–76.

    CAS  PubMed  Google Scholar 

  24. The Allen Mouse Brain Atlas. Accessed 15 May 2014.

  25. The Allen Developing Mouse Brain Atlas. Accessed 18 Sept 2017.

  26. Kanjhan R, Noakes PG, Bellingham MC. Emerging roles of Filopodia and dendritic spines in Motoneuron plasticity during development and disease. Neural Plast. 2016;2016:3423267.

    PubMed  Google Scholar 

  27. Vaughn JE, Henrikson CK, Grieshaber JA. A quantitative study of synapses on motor neuron dendritic growth cones in developing mouse spinal cord. J Cell Biol. 1974;60(3):664–72.

    CAS  PubMed  PubMed Central  Google Scholar 

  28. Vaughn JE, Sims T, Nakashima M. A comparison of the early development of axodendritic and axosomatic synapses upon embryonic mouse spinal motor neurons. J Comp Neurol. 1977;175(1):79–100.

    CAS  PubMed  Google Scholar 

  29. Vaughn JE, Barber RP, Sims TJ. Dendritic development and preferential growth into synaptogenic fields: a quantitative study of Golgi-impregnated spinal motor neurons. Synapse. 1988;2(1):69–78.

    CAS  PubMed  Google Scholar 

  30. Vaughn JE. Fine structure of synaptogenesis in the vertebrate central nervous system. Synapse. 1989;3(3):255–85.

    CAS  PubMed  Google Scholar 

  31. Tepper JM, Sharpe NA, Koos TZ, Trent F. Postnatal development of the rat neostriatum: electrophysiological, light- and electron-microscopic studies. Dev Neurosci. 1998;20(2–3):125–45.

    CAS  PubMed  Google Scholar 

  32. Lane PW, Ganser AL, Kerner AL, White WF. Spasmodic, a mutation on chromosome 11 in the mouse. J Hered. 1987;78(6):353–6.

    CAS  PubMed  Google Scholar 

  33. Ryan SG, Buckwalter MS, Lynch JW, Handford CA, Segura L, Shiang R, et al. A missense mutation in the gene encoding the alpha 1 subunit of the inhibitory glycine receptor in the spasmodic mouse. Nat Genet. 1994;7(2):131–5.

    CAS  PubMed  Google Scholar 

  34. Saul B, Schmieden V, Kling C, Mulhardt C, Gass P, Kuhse J, et al. Point mutation of glycine receptor alpha 1 subunit in the spasmodic mouse affects agonist responses. FEBS Lett. 1994;350(1):71–6.

    CAS  PubMed  Google Scholar 

  35. Chai CK. Hereditary spasticity in mice. J Hered. 1961;52(5):241–3.

    Google Scholar 

  36. Kingsmore SF, Giros B, Suh D, Bieniarz M, Caron MG, Seldin MF. Glycine receptor beta-subunit gene mutation in spastic mouse associated with LINE-1 element insertion. Nat Genet. 1994;7(2):136–42.

    CAS  PubMed  Google Scholar 

  37. Gomeza J, Ohno K, Hulsmann S, Armsen W, Eulenburg V, Richter DW, et al. Deletion of the mouse glycine transporter 2 results in a hyperekplexia phenotype and postnatal lethality. Neuron. 2003;40(4):797–806.

    CAS  PubMed  Google Scholar 

  38. Feng GP, Tintrup H, Kirsch J, Nichol MC, Kuhse J, Betz H, et al. Dual requirement for gephyrin in glycine receptor clustering and molybdoenzyme activity. Science. 1998;282(5392):1321–4.

    CAS  PubMed  Google Scholar 

  39. Kirsch J, Wolters I, Triller A, Betz H. Gephyrin antisense oligonucleotides prevent glycine receptor clustering in spinal neurons. Nature. 1993;366(6457):745–8.

    CAS  PubMed  Google Scholar 

  40. Grillon C. Models and mechanisms of anxiety: evidence from startle studies. Psychopharmacology. 2008;199(3):421–37.

    CAS  PubMed  Google Scholar 

  41. Ciuman RR. The efferent system or olivocochlear function bundle — fine regulator and protector of hearing perception. Int J Biomed Sci. 2010;6(4):276–88.

    PubMed  PubMed Central  Google Scholar 

  42. Galambos R. Suppression of auditory nerve activity by stimulation of efferent fibers to cochlea. J Neurophysiol. 1956;19(5):424–37.

    CAS  PubMed  Google Scholar 

  43. Desmedt JE, Monaco P. Mode of action of the efferent olivo-cochlear bundle on the inner ear. Nature. 1961;192:1263–5.

    CAS  PubMed  Google Scholar 

  44. Fex J. Auditory activity in centrifugal and centripetal cochlear fibres in cat. A study of a feedback system. Acta Physiol Scand Suppl. 1962;189:1–68.

    CAS  PubMed  Google Scholar 

  45. Wiederhold ML, Kiang NY. Effects of electric stimulation of the crossed olivocochlear bundle on single auditory-nerve fibers in the cat. J Acoust Soc Am. 1970;48(4):950–65.

    CAS  PubMed  Google Scholar 

  46. Liberman MC, Brown MC. Physiology and anatomy of single olivocochlear neurons in the cat. Hear Res. 1986;24(1):17–36.

    CAS  PubMed  Google Scholar 

  47. Yoshimi K, Kunihiro Y, Kaneko T, Nagahora H, Voigt B, Mashimo T. ssODN-mediated knock-in with CRISPR-Cas for large genomic regions in zygotes. Nat Commun. 2016;7:10431.

    CAS  PubMed  PubMed Central  Google Scholar 

  48. Hashimoto M, Takemoto T. Electroporation enables the efficient mRNA delivery into the mouse zygotes and facilitates CRISPR/Cas9-based genome editing. Sci Rep. 2015;5:11315.

    CAS  PubMed  PubMed Central  Google Scholar 

  49. Schneider CA, Rasband WS, Eliceiri KW. NIH image to ImageJ: 25 years of image analysis. Nat Methods. 2012;9(7):671–5.

    CAS  PubMed  PubMed Central  Google Scholar 

  50. Fujimoto C, Iwasaki S, Urata S, Morishita H, Sakamaki Y, Fujioka M, et al. Autophagy is essential for hearing in mice. Cell Death Dis. 2017;8(5):e2780.

    CAS  PubMed  PubMed Central  Google Scholar 

Download references


The authors thank Dr. M Watanabe (Hokkaido University) for providing antibodies. We acknowledge support by the CDBIM animal facilities. We thank Jeremy Allen, PhD, from Edanz Group ( for editing a draft of this manuscript.


This work was supported by JSPS KAKENHI Grant Number 17H03563 and 17 K14973.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Author information

Authors and Affiliations



MK designed, performed and analyzed all the experiments except ABR and wrote the paper. SU, SO and TY arranged and performed the ABR measurement and analyzed the results. YS provided technical assistance and contributed to preparation of the Figs. AA and KN contributed to generation and behavioral analysis of the Lamp5 mutant mice. TF conceived and coordinated the study. All authors reviewed the results, revised the paper and approved the final version of manuscript.

Corresponding author

Correspondence to Teiichi Furuichi.

Ethics declarations

Ethics approval

All animals were treated according to the recommendations and the protocols approved by the Animal Care and Use Committee of Tokyo University of Science and by the Animal Welfare Committee of the University of Tokyo.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no conflicts of interest with the contents of this article.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Additional file

Additional file 1:

Specificity of the anti-LAMP5 antibody in immunohistochemical staining. (PNG 348 kb)

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, 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 ( applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Koebis, M., Urata, S., Shinoda, Y. et al. LAMP5 in presynaptic inhibitory terminals in the hindbrain and spinal cord: a role in startle response and auditory processing. Mol Brain 12, 20 (2019).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: