Interaction of Acetylcholinesterase with Neurexin-1β regulates Glutamatergic Synaptic stability in Hippocampal neurons
- Yun-Yan Xiang†1, 2,
- Haiheng Dong†3,
- Burton B Yang4,
- John F MacDonald1, 2 and
- Wei-Yang Lu1, 2, 3, 5Email author
© Xiang et al.; licensee BioMed Central Ltd. 2014
Received: 13 October 2013
Accepted: 27 February 2014
Published: 5 March 2014
Excess expression of acetylcholinesterase (AChE) in the cortex and hippocampus causes a decrease in the number of glutamatergic synapses and alters the expression of neurexin and neuroligin, trans-synaptic proteins that control synaptic stability. The molecular sequence and three-dimensional structure of AChE are homologous to the corresponding aspects of the ectodomain of neuroligin. This study investigated whether excess AChE interacts physically with neurexin to destabilize glutamatergic synapses.
The results showed that AChE clusters colocalized with neurexin assemblies in the neurites of hippocampal neurons and that AChE co-immunoprecipitated with neurexin from the lysate of these neurons. Moreover, when expressed in human embryonic kidney 293 cells, N-glycosylated AChE co-immunoprecipitated with non-O–glycosylated neurexin-1β, with N-glycosylation of the AChE being required for this co-precipitation to occur. Increasing extracellular AChE decreased the association of neurexin with neuroligin and inhibited neuroligin-induced synaptogenesis. The number and activity of excitatory synapses in cultured hippocampal neurons were reduced by extracellular catalytically inactive AChE.
Excessive glycosylated AChE could competitively disrupt a subset of the neurexin–neuroligin junctions consequently impairing the integrity of glutamatergic synapses. This might serve a molecular mechanism of excessive AChE induced neurodegeneration.
KeywordsProtein interaction Glycosylation Neurodegeneration Synaptic apoptosis
As the key enzyme that hydrolyzes acetylcholine, acetylcholinesterase (AChE) plays a critical role in regulating cholinergic signaling. Neurons in the central nervous system generate two isoforms of AChE: synaptic AChE (AChE-S, also known as “tailed AChE”) and read-through AChE (AChE-R). In adults, AChE-S is the predominant isoform, although AChE-R increases following exposure to a variety of stressors. In the extracellular space, AChE exists in both soluble and membrane-bound forms. Soluble AChE includes monomeric AChE-R, as well as globular monomers and dimers of AChE-S. Membrane-bound AChE consists of AChE-S tetramers tethered to the cell membrane by a proline-rich membrane anchor. Interestingly, membrane-bound AChE-S can be released in response to cholinergic activation. Collective data imply that the isoforms, concentrations and localization of AChE within the brain are dynamically regulated.
In the brain, AChE is produced by cholinergic neurons, cholinoceptive neurons, and astrocytes. Clinical studies have indicated that an increase in anomalous AChE is strongly correlated with the pathogenesis of Alzheimer disease (AD)[7–10]. Specifically, AChE is a major component of amyloid-β (Aβ) plaques, and N- glycosylated AChE is increased in the cerebrospinal fluid of patients with AD. In particular, AChE binds to Aβ, thus promoting both the formation of Aβ fibrils and the occurrence of neurotoxicity. Moreover, augmenting AChE expression in the brains of transgenic mice that show neurodegeneration accelerates Aβ plaque formation. However, the molecular mechanism or mechanisms by which anomalous AChE contributes to the pathogenesis of AD remain uncertain.
A progressive loss of synapses in the cortex and hippocampus is characteristic of early-stage AD. Synaptic development and stability are regulated by the interaction of neurexin and neuroligin, transmembrane proteins that are expressed in the pre- and post-synaptic membrane domains of neurons, respectively[17, 18]. These two proteins connect via their ectodomains to form a trans-synaptic junction. Neurexin and neuroligin also interact, via their cytoplasmic tails, with the PDZ domains of specific scaffolding proteins in the pre- and post-synaptic compartments, respectively. In this way, the neuroligin–neurexin junctions promote trans-synaptic adhesion and assist in the assembly of pre- and post-synaptic specializations. Interestingly, the molecular sequence and three-dimensional structure of the ectodomain of neuroligins are homologous to the corresponding aspects of AChE. We previously showed that over-expression of AChE alters the expression of neurexins and neuroligins and decreases the number of glutamatergic synapses in hippocampal neurons. The objective of the present study was to determine if increased expression of AChE leads to a decrease in the neurexin–neuroligin junctions and consequently to a reduction in glutamatergic synapses.
Interaction between AChE and neurexins in Hippocampal neurons
Regulation of AChE–neurexin interaction by protein glycosylation
Mammalian neurons express both AChE-R and AChE-S, with each isoform displaying distinctive properties in molecular assemblies. To study which AChE isoform interacts with neurexin-1β, we expressed Nrxn-1β-1’-His with either hAChE-S or hAChE-R in HEK293 cells. We began with outlining the expression profiles of these proteins in the transfected cells.
To study the glycosylation pattern of AChE in mammalian cells, lysate of HEK293 cells transfected with AChE-R was treated with N- or O-glycohydrolases, both separately and in combination (Figure 2C). In another set of experiments, HEK293 cells transfected with AChE-S were treated with the N-glycosylase inhibitor tunicamycin (Figure 2D). Notably, immunoblotting of AChE-R from the cell lysate treated with the N-glycohydrolase PNGase F (Figure 2C) or from the lysate of AChE-S transfected cells treated with tunicamycin (Figure 2D) disclosed a single protein band, representing non-glycosylated AChE monomers. Specifically, the molecular weight of non-glycosylated AChE-R was about 64 kDa (Figure 2C), whereas the molecular weight of non-glycosylated AChE-S was about 62 kDa (Figure 2D). In contrast, immunoblotting AChE from the cell lysates treated with the O-linked glycohydrolases O-glycosidase and sialidase, separately or in combination, revealed two protein bands with the same molecular weights as the control (Figure 2C). These results confirm the previously reported finding that AChE molecules are highly modified by N-glycosylation[26, 30, 31], but not by O-glycosylation.
We also studied the glycosylation pattern of neurexin-1β in HEK293 cells. Our immunoblotting assays showed that in the total cell lysates treated with the O-glycohydrolases O-glycosidase and sialidase, the 73-kDa band of neurexin-1β disappeared while the density of the 58-kDa band of neurexin-1β increased dramatically (Figure 3C, left panel). These results indicate that the 73 kDa neurexin-1β band represents O-glycosylated forms. Notably, treating the transfected cells with tunicamycin (Figure 3C, right panel) and treating the lysates of transfected cells with PNGase F (Figure 3C, left panel) caused a slight reduction in the molecular weight of all neurexin-1β protein bands, from 55, 58 and 73 kDa, respectively, to about 53, 56 and 71 kDa, respectively. These results imply that short sugar chains are linked to O-glycosylated forms of neurexin-1β proteins by N-glycosylation, with the 53-kDa band representing the non-glycosylated form. Collectively, our results confirm a previous finding that neurexin-1β has minor N-glycosylation, and the various molecular weights of neurexin-1β primarily reflect various degrees of O-glycosylation. In addition, our assays indicate that a large amount of neurexin-1β proteins located in the cell membrane is O-glycosylated.
Modulation of AChE–neurexin interaction by β-neurexin splicing and AChE ligand
Interaction of neurexins with neuroligins decreases when the 30 amino acid insert SS4 is present in the laminin G domain of β-neurexins. To determine whether SS4 affects the interaction AChE with neurexin-1β, we co-immunoprecipitated the lysates of two sets of HEK293 cells: one set of cells transfected with hAChE-S and Nrxn-1β-1’-His (without SS4) and another set of cells transfected with hAChE-S and Nrxn-1β-3’-His (with SS4) using anti-AChE. Similar to the non-O-glycosylated Nrxn-1β-1’ (Figure 4D, lanes 1 and 2), non-O-glycosylated Nrxn-1β-3’ molecules were also co-precipitated by anti-AChE, displaying as two bands at molecular weights of about 57 and 60 kDa, respectively (Figure 4D, lanes 3 and 4). However, at the same quantity of cell lysate proteins, the amount of co-precipitated Nrxn-1β-3’ (Figure 4D, lane 3) was less than that of co-precipitated Nrxn-1β-1’ (Figure 4D, lane 1). This result implies that alternative splicing of the SS4 in Nrxn-1β regulates the interaction between AChE–neurexin to some extent.
Surface anionic residues expressed on the esterase side of AChE allow this molecule to interact with various proteins[35–38]. To study whether some AChE ligands and/or inhibitors regulate interactions between AChE and neurexin, we examined co-immunoprecipitates of lysates of A549 cells transfected with hAChE-S combined with either Nrxn-1β-1’-His or with Nrxn-1β-1’-His in the absence or presence of the AChE inhibitor physostigmine (10 μM, added to the culture medium). Interestingly, physostigmine enhanced co-precipitation of AChE-S with neurexin-1β-1’ and with neurexin-1β-3’ (Figure 4D, lanes 2 and 4), which suggests that the AChE ligand may structurally regulate the interaction of AChE with neurexin.
AChE interacts only with neurexin-1β located in cell membrane
To test our hypothesis that AChE interacts with the ectodomain of β-neurexin, we transfected one set of HEK293 cells with Nrxn-1β-1’-His and another set of HEK293 cells with AChE-S. Sixteen hours after transfection, we co-cultured the two sets of transfected cells for another 24–32 hours in the absence or presence of physostigmine. Immunoprecipitating the lysate of these co-cultured cells with anti-AChE led to co-precipitation of the 55-kDa Nrxn-1β-1’ protein, which was confirmed by blotting His (Figure 4E, lane 2). Again, physostigmine increased the band density of co-precipitated Nrxn-1β-1’ (Figure 4E, lane 3). This result confirms that AChE interacts with the ectodomain of neurexin-1β. In another experiment, we mixed the lysate of cells transfected with AChE-S with the lysate of cells transfected with Nrxn-1β-1’-His. In this test, anti-AChE did not co-precipitate any Nrxn-1β-1’ from the cell lysate mixture, even in the presence of physostigmine (not shown). Together, these combined results suggest that AChE interacts only with β-neurexins located on the cell membrane.
Excess AChE decreases the neurexin–neuroligin association
Next, we tested whether the disruption of the neurexin–neuroligin association caused by excess AChE leads to interruption of synaptic stability. Axonal terminals that pass through non-neuronal cells transfected with neuroligin-1 initiate presynaptic differentiation, expressing presynaptic proteins and forming presynaptic structures; such synaptogenic activities are initiated by the interaction between β-neurexin and neuroligin. Using this cellular model, we examined whether excess AChE in the extracellular space could alter the neurexin-neuroligin interaction induced presynaptic maturation. As previously reported, we found that the axonal neurites of embryonic hippocampal neurons developed synapsin-immunoreactive presynaptic buttons on HEK293 cells expressing neuroligin-1 (Figure 5B, middle row), and such button-like presynaptic structures were not formed by axonal neurites on control HEK293 cells (Figure 5B, top row). This result confirms that neuroligin-1 does indeed initiate development of presynaptic structures. Importantly, we found that culturing the neuroligin-1-expressing HEK293 cells in the AChE-S-conditioned medium (with 5 μM physostigmine) greatly decreased the number of synapsin-immunoreactive presynaptic buttons on neuroligin-expressing cells (Figures 5B and C). Together, these results imply that excess extracellular AChE could inhibit synaptic development or interrupt synaptic stability, by reducing the association of β-neurexin with neuroligin.
Excess AChE reduces glutamate-induced currents in Hippocampal neurons
Excess extracellular AChE decreases glutamatergic synapses in primary neurons
The activity and expression levels of AChE control the amount of extracellular acetylcholine, which critically regulates glutamatergic synaptic transmission. AChE has non-catalytic functions in vitro[40, 41] and in vivo, some of which likely involve protein–protein interactions. Consistent with this notion, the present study revealed that excess N-glycosylated AChE alters the structure and function of glutamatergic synapses through its interaction with non-O-glycosylated neurexins and a consequent reduction in the association between neurexin and neuroligin. These findings delineate a molecular mechanism whereby excess glycosylated AChE could contribute to neurological disorders in the brain. Previous studies have shown that increased expression of AChE in cortical neurons reduces the number of synapses and the levels of β-neurexins both in vivo[43, 44] and in vitro. These results suggest crosstalk between AChE and neurexin. We hypothesized that these two proteins might interact physically and anticipated that they would be co-located in primary neurons. Indeed, our immunocytochemical assays showed that many AChE assemblies in neurites were co-localized with neurexin clusters (Figure 1A-1), which implies a potential in situ association between the two molecules. In addition, AChE could be reciprocally co-precipitated with neurexin-1β from the lysates of cultured neurons (Figure 1B, middle lane). Furthermore, as previously reported, treating neurons with the selective AChE inhibitor BW284c51 enhanced the expression of AChE (Figure 1B) and increased the co-precipitation of AChE with neurexin (Figure 1C, right lane). Together, these results imply that interactions of AChE with neurexin occur in primary neurons.
The interaction between AChE and neurexin was further substantiated by assaying lysates of HEK293 cells that had been transfected with hAChE-R or AChE-S, either separately or in combination with Nrxn-1β-1’ or with Nrxn-1β-3’. Under natural conditions, AChE-R formed only monomers, whereas AChE-S existed as monomers and possibly dimers (Figures2A and 2B). As previously reported, under denaturing conditions (i.e., in the presence of N-glycohydrolase), both isoforms of AChE appeared as glycosylated monomers with reduced molecular weight (Figure 2C). Under denaturing conditions, neurexin-1β in cell lysates and membrane fractions also exhibited glycosylated forms (Figures 3A and B). Specifically, a large amount of neurexin-1β proteins in HEK293 cells had large molecular weights (73 kDa) as they were associated with both N- and O-linked glycans, while a lesser quantity of neurexin-1β exhibited smaller molecular weights (55 and 58 kDa) because they had only N-glycosylation.
Remarkably, monomers of both AChE-S and AChE-R were reciprocally co-immunoprecipitated only with the N-glycosylated (55 and 58 kDa) neurexin-1β proteins, not with the O-glycosylated (73 kDa) forms (Figures 4A and B). These results are in accord with those of an earlier study in which no interaction of AChE with the 72-kDa neurexin-1β was detected. However, our observation of co-immunoprecipitation of neuronal AChE variants with non-O-glycosylated β-neurexins was novel. Previous studies showed that AChE-S and AChE-R differ in structure of C-terminals and have inverse effects on amyloid fibrils formation[47, 48], implying that the two neuronal AChE variants may have distinctive roles in AD pathology. Therefore, the significance of interactions between the non-O-glycosylated β-neurexins and the two AChE variants awaits further studies.
The AChE–β-neurexin interaction requires N- glycosylation of either AChE or neurexin-1β, because there was no co-precipitation of neurexin-1β with AChE when the N-glycosylases were inhibited (Figure 4C, lane 4). In addition, co-precipitation of AChE and neurexin was observed in the lysate of co-cultured cells that had been transfected with either AChE-S or Nrxn-1β-1’ before co-culturing (Figure 4E); in contrast, co-precipitation was not observed in a mixture of lysates from cells that were separately transfected with either AChE-S or Nrxn-1β-1’ (not shown). These results indicate that AChE monomers interact with the extracellular domain of β-neurexins, specifically those located in the cell membrane.
Although the association between neurexin and neuroligin is essential for both excitatory and inhibitory synapses, neuroligin varies in terms of the isoforms present at excitatory and inhibitory synapses. Specifically, neuroligin-1 is primarily localized at glutamatergic synapses, whereas neuroligin-2 is largely restricted to GABAergic synapses. In the present study, AChE exhibited greater affinity for neurexin-1β-1’ (lacking the SS4 insert) (Figure 4D). Given that neurexin-1β-1’ has a higher affinity for neuroligin-1 and a lower affinity for neuroligin-2, it is plausible that AChE preferentially disrupts the interaction between neurexin-1β-1’ and neuroligin-1 at glutamatergic synapses. Indeed, increased expression of AChE reduces the cell surface clusters of glutamate receptor subunits but increases the total proteins of neuroligin, glutamate receptor subunits and postsynaptic density protein 95 (PSD-95) in hippocampal neurons, which together imply that excess AChE decreases glutamatergic synapses and thus allows cellular accumulation of postsynaptic proteins. Nevertheless, the issue as to whether AChE does not disrupt the association between neurexin-1β and neuroligin-2 but selectively interrupts the association between neurexin-1β and neuroligin-1, requires more detailed studies.
Bi-directional signaling by adhesion molecules in the pre- and post-synaptic compartments determines the appropriate differentiation of synaptic structures. The interaction of neurexins and neuroligins mediates signaling across the synapse and ultimately shapes the properties of neural networks. Previous studies have demonstrated that glycosylation of neurexin-1β is required for such interactions. In the current study, the majority of membrane-targeted β-neurexins were modified by both O- and N-glycosylation, whereas a small number of β-neurexins in the membrane were linked only with N-glycans (Figure 3). Interestingly, AChE monomers interacted only with the non-O-glycosylated β-neurexins (Figures 3 and4), and such interactions might fine-tune synaptic stability (Figures 7 and8), probably possibly through modulation of the neurexin–neuroligin association (Figure 5).
Another important outcome of this study was the finding that the AChE-neurexin interaction requires AChE N-glycosylation (Figure 4C, lane 4). Given that N- glycosylated AChE is significantly increased in the cerebrospinal fluid of patients with AD, and that the expression of AChE is negatively regulated by miR-132, which largely decreases in late-onset AD patients, it is plausible that the interaction between AChE and neurexin increases in the brains of AD patients, leading to damage at the glutamatergic synapses. We propose that under normal physiological conditions, a low concentration of N-glycosylated AChE is present at glutamatergic synapses, which has little effect on the synaptic stability (Figure 9). However, under pathological conditions such as AD, the quantity of N-glycosylated AChE monomers in the brain increases greatly, to the point where the monomers interact with β-neurexins, adversely affecting the structure and function of a subset of glutamatergic synapses. Such action of excessive AChE may also link to other cognitive diseases, for example autism, because alterations in cholinergic activity and/or in neuroligin-neurexin association in the brain lead to autism spectrum disorders.
In summary, our studies demonstrated that excess glycosylated AChE could interact with non-O-glycosylated neurexin-1β, thus competitively disrupting a subset of the neurexin–neuroligin junctions and consequently impairing the integrity of some glutamatergic synapses. Our findings may provide a molecular mechanism of excessive AChE induced neurodegeneration.
Complementary DNA construction
Complementary DNA (cDNA) encoding full-length human AChE-S (hAChE-S), inactive hAChE-S (hAChE-Sin) and human AChE-R (hAChE-R) cloned into the pL5CA expression vector were gifts from Dr. Hermona Soreq at the Hebrew University of Jerusalem. cDNA encoding a full-length rat neuroligin-1 cloned in the pCMV5 expression vector (pCMVNL1), cDNA encoding a rat neurexin-1β lacking alternatively spliced sequence 4 (SS4) (neurexin-1β-1’) from pCMVN1β-1 and cDNA encoding a full-length rat neurexin-1β containing SS4 (neurexin-1β-3’) from pCMVN1β-3 were gifts from Dr. Thomas C. Südhof at Stanford University. To obtain better immunobiochemical signals for neurexins, the neurexin cDNA samples were inserted into a pcDNA3 expression vector tagged with 6-His[71, 72]. Briefly, the cDNA for full-length neurexin-1β-1’ and neurexin-1β-3’ was amplified by polymerase chain reaction using platinum Pfx DNA polymerase (Invitrogen, Carlsbad, CA) from pCMVN1ß-1 and pCMVN1ß-3 cDNA, respectively. The product of the polymerase chain reaction was inserted into the BamHI-XbaI site of the pcDNA3, positioned in frame upstream to the 6-His epitope and followed by a stop codon. All constructs were re-sequenced, with confirmation of the absence of nucleotide errors and the in-frame context of the neurexin cDNA with 6-His. cDNA encoding His-tagged rat neurexin-1β from those vectors was named neurexin-1β-1’-His (Nrxn-1β-1’-His) and neurexin-1β-3’-His (Nrxn-1β-3’-His), respectively.
Human embryonic kidney 293 (HEK293) cells were maintained in Dulbecco’s modified Eagle medium (DMEM) supplemented with 10% fetal calf serum in a 37°C humidified atmosphere containing 5% CO2. Cells at 75% confluence were transiently transfected with cDNA encoding hAChE-S, hAChE-Sin or hAChE-R or with the expression vector alone, using Lipofectamine 2000 transfection reagent (Invitrogen), according to the manufacturer’s instructions. Twelve hours after transfection, the DMEM was replaced with fresh B27-supplemented Neurobasal medium (1:50, Invitrogen). Twenty-four hours later, the hAChE-conditioned media and the hAChE-free conditioned medium (from cells transfected with expression vector alone) were collected. Previous work has shown that recombinant hAChE is secreted from transiently transfected HEK293 cells as a soluble globular enzyme. The presence of active hAChE in the conditioned medium was confirmed by an AChE activity assay according to Ellman’s method, as previously described. The presence of catalytically inactive hAChE-S (hAChE-Sin) in its conditioned medium was confirmed by immunoblot assays.
Culture of Hippocampal neurons
Neuronal cell dissociation and culture were performed as previously described[21, 74]. Briefly, hippocampal cells from Wistar rat embryos at day 18 (E18) were isolated by mechanical trituration. The dissociated cells were cultured on dishes or coverslips coated with poly-d-lysine (Sigma, Oakville, Canada) at a density of 3 × 10 cells/cm2 in standard plating medium containing B27-supplemented Neurobasal medium, 0.5 mM l-glutamine, 25 μM glutamic acid, 0.5 mM sodium pyruvate and 0.5% fetal bovine serum. The hippocampal cells were incubated for 18 hours at 37°C in an atmosphere containing 5% CO2, after which the plating medium was replaced with culture medium containing B27-supplemented Neurobasal medium and l-glutamine (0.5 mM). This culture medium supports neuronal growth while restricting the growth of other cell types. According to the requirements of specific experiments, the neurons were treated and used at various days in vitro (DIV).
To investigate whether an increase in AChE expression affects neuronal function, two sets of cultured hippocampal neurons at the fifth DIV were transfected (using Lipofectamine 2000 transfection agent) with cDNA, one set with cDNA encoding hAChE-S and the other set with cDNA encoding hAChE-R, along with a green fluorescent protein (GFP)-encoding vector. Neurons transfected with both the pL5CA expression vector and the GFP-encoding vector were used as controls. Three hours after transfection, the transfection medium was replaced with fresh B27-supplemented Neurobasal medium. To eliminate the catalytic action of excessive AChE, the AChE inhibitors physostigmine (10 μM, Sigma) or 1, 5-bis (4-allyldimethylammoniumphenyl)-pentan-3-one dibromide (BW284c51, 5 μM, Sigma) was added to the media. Twelve to fourteen hours after transfection, a fluorescence microscope was used to identify the transfected neurons (labeled with GFP fluorescence), and the transfection rate was calculated. To study whether excess AChE impairs neuronal function by an extracellular mechanism, other sets of cultured hippocampal neurons at the fifth DIV were treated with AChE-conditioned media or medium to which purified hAChE-S had been added (Sigma, C-1682; generated from the same hAChE cDNA used in this study) in the presence of physostigmine (10 μM).
Immunocytochemical assays in cultured neurons
Immunocytochemical assays were performed as previously described[21, 74], with minor modifications. Briefly, live cultured hippocampal neurons at the 11th DIV, with or without BW284c51 treatment (5 μM, for 3 days), were incubated with anti-AChE antibody (Chemicon, Temecula, CA, diluted 1:100 in the medium) for 2 hours. After washing with phosphate-buffered saline (PBS), the neuronal cells were fixed with 3.7% paraformaldehyde and 4% sucrose in PBS for 10 minutes. Following incubation with a Cy3-conjugated donkey anti-mouse secondary antibody (Jackson ImmunoResearch Laboratories, West Grove, PA), the cells were permeabilized with 0.1% Triton X-100 for 10 minutes, blocked in 5% normal donkey serum for 1 hour and then incubated with anti-neurexin antibody (Santa Cruz Biotechnology, Santa Cruz, CA, 1:100) at 4°C overnight. Following three gentle washes, cells were incubated with fluorescein isothiocyanate-conjugated donkey anti-goat secondary antibody (Jackson ImmunoResearch Laboratories) for 1 hour. For immunocytochemical assays of the glutamate receptor subunit GluR2 (GluA2) and the presynaptic vesicular protein synapsin, cultured neurons at the ninth DIV were treated with AChE-conditioned medium or with AChE-free conditioned medium in the presence of 10 μM physostigmine. At the 12th DIV, the treated neurons were fixed with 3.7% paraformaldehyde and 4% sucrose in PBS for 15 minutes and were then permeabilized in 0.1% Triton X-100 for 10–15 minutes. Following 1 hour of blocking with 5% goat serum, the cells were incubated with anti-GluR2 or anti-synapsin (Chemicon, 1:1000).
Visual fields under a confocal microscope (Carl Zeiss, Gottingen, Germany) were randomly selected by blindly moving the cell-culture coverslip. Dual immunofluorescence was captured in two-channel mode, as previously described. Digital images were obtained with a 63× objective lens. Multiple electronic images of cells were obtained and saved in a computer for analysis. For both control and treated neurons, the number of immunofluorescent protein particles was counted and the length of neurites was measured using Image J software (NIH Image, NIH, Bethesda, MD). This information was used to calculate the density of immunoreactive protein clusters, expressed as number of clusters per 20 μm length of dendrite. For colocalization analysis, confocal microscopic images of the two channels were background-subtracted and the threshold of fluorescent punctate structures at neuronal dendrites was set to the level at least twofold greater than the background. As previously described, colocalization was measured by means of Image J as the fraction of the image filed labeled for one channel that was also labeled for the second channel.
Co-immunoprecipitation of neurexin and AChE from cultured neurons
At the seventh DIV, the cultured hippocampal neurons, with or without BW284c51 treatment (5 μM, for 3 days), were lysed in a buffer containing 20 mM Tris–HCl (pH 7.5), 150 mM NaCl, 0.5% Triton X-100 and protease inhibitors. Cell lysate (500–1000 μl, concentration 1 μg/μl) was incubated with Protein A-Sepharose beads (Sigma) at 4°C for 30 minutes to remove nonspecific binding proteins. The cleared lysate was then incubated with anti-neurexin antibody (Santa Cruz Biotechnology) or anti-AChE antibody (BD Biosciences, Franklin Lakes, NJ) overnight at 4°C, to allow reciprocal co-immunoprecipitation of neurexin and AChE. For controls, cell lysate was incubated with the same amount of normal IgG (Santa Cruz Biotechnology) or without added antibody. After incubation with Protein A-Sepharose beads for 2 hours, the immunoprecipitates were washed three times with ice-cold lysis buffers, and the binding proteins were eluted with sample buffer. The AChE inhibitor BW284c51 (5 μM) was included in all buffers used for immunoprecipitation. The general procedures for Western blotting were the same as previously described. Briefly, after electro-transfer of the precipitates to nitrocellulose membrane (Bio-Rad, Hercules, CA), AChE or neurexin in the immunoprecipitated material was probed by immunoblotting with anti-AChE antibody (BD Biosciences) or anti-neurexin antibody (Santa Cruz Biotechnology).
Transfection of HEK293 cells with neurexin-1β and hAChE cDNA
To study whether specific AChE isoforms interact with neurexin-1β, HEK293 cells were transiently transfected with plasmid DNA encoding neurexin-1β and specific isoforms of hAChE, using Lipofectamine 2000 transfection agent according to the manufacturer’s protocol. Briefly, HEK293 cells at 70%–80% confluence were co-transfected with cDNA encoding Nrxn-1β-1’-His and either hAChE-S or hAChE-R. As controls, some cells were transfected with Nrxn-1β-1’-His, hAChE-S or hAChE-S-R cDNA alone. To study whether AChE interacts extracellularly with Nrxn-1β-1’-His on the cell membrane, one set of HEK293 cells was transfected with hAChE-S and another set with Nrxn-1β-1’-His. Five hours later, the HEK293 cells transfected with Nrxn-1β-1’-His were gently stripped off and then re-seeded onto the HEK293 cells transfected with hAChE-S (or onto cells transfected with control vector), at a ratio of 1:1.5. For all transfection operations, equal amounts of transfected DNA were obtained by adding vector DNA, and the catalytic action of AChE was blocked by adding physostigmine (10 μM) to the medium.
Characterization of transfected proteins in HEK293 cells
To detect AChE variants, HEK293 cells were lysed in a buffer containing 20 mM Tris–HCl (pH 7.5), 150 mM NaCl, 1% Triton X-100 and proteinase inhibitors. Immunoblotting of the cell lysate or the culture medium collected from the transfected cells was performed under non-reducing conditions. Specifically, the protein sample was applied to 10% gel using the loading buffer without the reducing agent, as described previously.
To study the glycosylation profiles of proteins expressed in HEK293 cells, protein samples obtained from the lysates of transfected cells or from the culture medium were denatured and incubated with peptide N-glycosidase F (PNGase F), O-glycosidase and /or sialidase using Enzymatic CarboRelease Kit (QA-Bio, Palm Desert, CA) for 3 hours at 37°C according to the manufacturer’s protocol and then processed for Western blotting. To study the effect of N-linked glycosylation on the interaction between AChE and β-neurexins, the transfected cells were treated (5 hours after transfection) with tunicamycin (0.5 μg/ml, Sigma), a selective inhibitor of N-glycosylase, or the equivalent volume of dimethyl sulfoxide (vehicle control). Cells were lysed 40–48 hours after transfection, and co-immunoprecipitation was performed as described above.
Membrane surface proteins in transfected HEK293 cells were examined by surface biotination of intact cells with EZ-Link Sulfo-NHS-SS-Biotin reagent (Pierce Biotechnology, Rockford, IL) according to the manufacturer’s protocol. Briefly, intact cells were washed and then incubated in the reagent (0.5 mg/ml in PBS, pH 8.0) for 1 hour on ice. Unbound biotin was quenched by incubation in 50 mM Tris, pH 8.0, for 10 minutes on ice. Cells were washed two times with ice-cold PBS and then lysed. The biotinylated proteins were precipitated by rocking with streptavidin beads (Pierce) overnight at 4°C. The beads were washed three times in lysis buffer, and bound proteins were eluted in sodium dodecyl sulfate sample buffer. The membrane proteins were confirmed by immunoblotting with specific antibodies.
Co-immunoprecipitation of protein samples from transfected HEK293 cells
Transfected HEK293 cells were used for co-immunoprecipitation assays 40–48 hours after transfection. Briefly, the transfected cells were lysed in ice-cold 1% Triton X-100 and 0.5% sodium deoxycholate in PBS supplemented with protease inhibitors. AChE and neurexin were co-immunoprecipitated by incubating the cleared lysates with anti-AChE antibody (Santa Cruz Biotechnology) or anti-His antibody (QIAGEN, Hilden, Germany) for 3 hours at 4°C. Physostigmine (10 μM) was included in all buffers used for immunoprecipitation. Neurexin or AChE in the immunoprecipitated material was probed by immunoblotting with anti-His followed by anti-mouse light-chain-specific secondary antibody (Jackson ImmunoResearch Laboratories) or with AChE antibody (Santa Cruz Biotechnology). To control for efficiency of transfection, the expression levels of all proteins were assessed by Western blotting. The blot films were scanned with a GS800 densitometer (Bio-Rad).
To investigate whether increased extracellular AChE interrupts the neurexin–neuroligin association, HEK293 cells were co-transfected with cDNA encoding Nrxn-1β-1’-His and neuroligin-1, and the transfected HEK293 cells were cultured in AChE-S-conditioned medium or AChE-free conditioned medium. Twenty-four hours after co-transfection, HEK293 cells were lysed as previously described, with minor modification, in a buffer containing (in mM) 20 Tris–HCl (pH 7.5), 100 NaCl, 4 KCl and 5 CaCl2, as well as 2% CHAPS cell lysis buffer and protease inhibitors, at 4°C. The cell lysate was cleared as described above and then incubated with anti-His antibody (QIAGEN), and the precipitated neuroligin was confirmed by immunoblotting with anti-neuroligin antibody (Synaptic Systems, Göttingen, Germany).
Co-culture of neurons with neuroligin-expressing HEK293 cells
HEK293 cells plated at low density on poly-D-lysine coated glass coverslips were cultured in DMEM. Five hours after plating, the medium was replaced with neuron plating medium, and dissociated E18 hippocampal cells (3 × 10 cells/cm) were plated onto the HEK293 cells. On the fifth day of co-culture, the cells were transfected with rat neuroligin-1 cDNA and the GFP-encoding vector, using Lipofectamine 2000 transfection agent. Five hours after transfection, the medium was replaced with AChE-conditioned medium or AChE-free conditioned medium in the presence of 10 μM physostigmine. Two days after transfection of neuroligin-1, the cells were processed according to the procedures used for neurons (see above) and then incubated with anti-synapsin (Chemicon, 1:1000) at 4°C overnight. Following incubation with Cy3-conjugated secondary antibodies at 4°C for 1 hour, the coverslips were rinsed and then mounted for confocal microscopic examination.
Patch-clamp recordings in cultured neurons
Control and treated neurons were used for patch-clamp recordings 40–48 hours after treatment. Transfected neurons were identified by green fluorescence, and a sample of these neurons was randomly selected for recordings. The procedures for voltage-clamp recording were as previously described. Briefly, recordings were obtained by means of an Axopatch-1D amplifier (Axon Instruments, Foster City, CA) with holding potential of −60 mV. The extracellular solution contained (in mM): 145 NaCl, 1.3 CaCl2, 5.4 KCl, 25 HEPES and 28 glucose, with pH 7.4 and osmolarity about 315 mOsm. The patch electrodes, made with thin-walled glass tubes, were filled with a solution containing (in mM) 150 KCl, 10 HEPES, 1 CaCl2, 2 MgCl2, 2 tetraethylammonium and 4 ATP, with pH 7.35 and osmolarity 310 mOsm. To study the effects of AChE on the function of the major transmitter receptors in neurons, glutamate-evoked and γ-aminobutyric acid (GABA)-evoked currents were studied. Rapid application of the receptor agonist was achieved with a computer-controlled, multibarrel-perfusion system (SF-77B, Warner Instruments, Hamden, CT). Electrical signals were digitized, filtered (1–2 kHz) and acquired on-line by means of the data acquisition and analysis software Clampex (Axon Instruments). The peak amplitude of evoked currents was measured off-line using Clampfit software (Axon Instruments). For recording of miniature excitatory postsynaptic currents (mEPSCs), 0.5 μM of tetrodotoxin and 20 μM of bicuculline methiodide were included in the ECS. All recordings were performed at room temperature (22-24°C). In each recording, at least 120- mEPSC events were collected for analysis. The amplitude and frequency of mEPSCs were analyzed using the program Mini-analysis (Synaptosoft Inc., Decatur, GA).
Statistical analyses were performed using Student’s unpaired or paired t tests as appropriate. Data are expressed as mean ± standard error of the mean (SEM). A p value < 0.05 was considered significant.
The authors sincerely thank Dr. Thomas C. Südhof for providing the complementary DNA (cDNA) encoding neurexin-1β and neuroligin-1 and Dr. Hermona Soreq for supplying the cDNA encoding synaptic and read-through acetylcholinesterase. This study was supported by the Canadian Institutes of Health Research (grants MOP-84517 and FRN 94359 to WYL).
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