Abstract
The molecules that specify domains on the neuronal plasma membrane for the delivery and accumulation of vesicles during neurite outgrowth and synapse formation are unknown. We investigated the role of the sec6/8 complex, a set of proteins that specifies vesicle targeting sites in yeast and epithelial cells, in neuronal membrane trafficking. This complex was found in layers of developing rat brain undergoing synaptogenesis. In cultured hippocampal neurons, the sec6/8 complex was present in regions of ongoing membrane addition: the tips of growing neurites, filopodia, and growth cones. In young axons, the sec6/8 complex was also confined to periodic domains of the plasma membrane. The distribution of synaptotagmin, synapsin1, sec6, and FM1–43 labeling in cultured neurons suggested that the plasma membrane localization of the sec6/8 complex preceded the arrival of synaptic markers and was downregulated in mature synapses. We propose that the sec6/8 complex specifies sites for targeting vesicles at domains of neurite outgrowth and potential active zones during synaptogenesis.
Neurons undergo a characteristic sequence of developmental events culminating in the formation of synapses. Initially, neurons polarize, elaborating functionally and morphologically distinct axons and dendrites (Dotti et al., 1988; Craig and Banker, 1994). This polarization arises, in part, through the specific intracellular trafficking of lipid and protein components, via vesicle intermediates, to appropriate locations in the cell (Calakos and Scheller, 1996). Vesicle trafficking is crucial for the membrane addition, which allows dynamic restructuring of axonal and dendritic plasma membrane in the process of neurite outgrowth. An important neurobiological question is how the vesicle-mediated membrane addition that underlies neurite outgrowth is accomplished. Studies of solubleN-ethylmaleimide-sensitive factor attachment protein receptors (SNAREs), a family of proteins which may negotiate vesicle and target membrane interactions, have provided much insight into the molecular mechanisms of secretion (Scheller, 1995; Sudhof, 1995). Vesicles are endowed with v-SNAREs of the vesicle-associated membrane protein (VAMP) family, which allow them to interact specifically with t-SNAREs of the syntaxin family located on the target membrane (Hay and Scheller, 1997). These interactions may be crucial mediators of membrane fusion events (Broadie et al., 1995; Hanson et al., 1997; Lin and Scheller, 1997; Weber et al., 1998). However, SNAREs of the syntaxin family are broadly localized along the plasma membrane (see Fig. 3) and thus are probably not important for targeting of vesicles to specific domains (Galli et al., 1995). The molecules that define targeting domains for polarized constitutive secretion in neurons have yet to be described.
Targeting of vesicles to synaptic sites during development may use similar mechanisms as those involved in vesicle fusion underlying membrane outgrowth. Before contact with a postsynaptic target, axons possess mobile vesicle clusters bearing synaptotagmin, which fuse with the plasma membrane after stimulation (Matteoli et al., 1992;Kraszewski et al., 1995; Dai and Peng, 1996). Thus, growing axons must contain the molecular machinery required for constitutive exocytosis, endocytosis, and activity-dependent vesicle release. However, it is unclear how vesicles become clustered at synapses. Although vesicle fusion in axons might occur anywhere along the plasma membrane, there must be membrane targets that signal the clustering of vesicles for synapse formation. Furthermore, it is unclear how sites of vesicle exocytosis are modified as the neuron forms stable contacts with postsynaptic partners.
One candidate for a vesicle targeting signal important in polarized exocytosis is the mammalian sec3/5/6/8/10/15/exo70/exo84 (sec6/8 or exocyst) complex. Supporting evidence comes from studies of the yeastSaccharomyces cerevisiae, mammalian epithelial cells (see Fig. 9), and rat brain. Most of the components of the yeast sec6/8 complex were initially discovered in a screen for secretory mutants in yeast and are homologs of members of the mammalian complex (Novick et al., 1980; Bowser and Novick, 1991; Bowser et al., 1992; Potenza et al., 1992; Ting et al., 1995; Hsu et al., 1996; TerBush et al., 1996;Guo et al., 1997; Hazuka et al., 1997; Kee et al., 1997). The yeast sec6/8 complex is associated with the plasma membrane and is highly concentrated at sites of active vesicle exocytosis: at the tip of a new growing bud (TerBush and Novick, 1995; Drubin and Nelson, 1996; TerBush et al., 1996; Finger and Novick, 1997; Finger et al., 1998) and just before cytokinesis at the neck of budding cells (Monde’sert et al., 1997). As in yeast, members of the mammalian sec6/8 complex associate to form a stable 17S particle, which is present in rat brain (Hsu et al., 1996) and epithelial cells (Grindstaff et al., 1998). In polarized Madin–Darby canine kidney (MDCK) epithelial cells, antibodies directed against rat sec8 block vesicle secretion at the basolateral membrane (Grindstaff et al., 1998). The sec6/8 complex is believed to act at the plasma membrane, upstream of the membrane fusion machinery, and is expressed in all tissues examined, suggesting an important role in constitutive vesicle targeting (Ting et al., 1995; Hazuka et al., 1997; Kee et al., 1997). These data are consistent with the hypothesis that the sec6/8 complex plays a role in the accumulation of vesicles at the plasma membrane, which is essential for polarized vesicle targeting.
We provide evidence that in addition to a role in the polarized exocytosis underlying neurite outgrowth, the sec6/8 complex is important for the formation of synapses. In slices of brain tissue and in cultured hippocampal neurons, the sec6/8 complex was highly expressed in regions undergoing neurite outgrowth and synaptogenesis. During synaptogenesis, expression of the sec6/8 complex along axons preceded the arrival of synaptic markers and then, later in development, colocalized with synapsin1 and FM1–43. However, in older neurons, sec6/8 complex localization at synapses was greatly reduced. These data point to roles for the sec6/8 complex in targeted vesicle secretion important for neurite outgrowth, as well as the development of synaptic release sites, and suggest that the complex is an early, transient marker for potential synapses.
MATERIALS AND METHODS
Brain sectioning and immunolabeling. Brains were removed from embryonic day 18 (E18) embryos, immediately submerged in 4% paraformaldehyde (PF) in PBS for 4 hr, and then transferred to 20% sucrose–4% PF in PBS for 24 hr. Sixteen micrometer sections were cut using a cryostat, and sections were applied to Superfrost*/Plus slides (Fisher Scientific, Pittsburgh, PA). Adult and postnatal day 5 (P5) rats were perfused intracardially with 4% PF in PBS. The brains were removed and submerged in 4% PF in PBS for 1 hr, then transferred to 20% sucrose–4% PF in PBS for 36 hr, and sectioned (35 μm) on a freezing microtome. Sections from both fixation methods were then washed and blocked–permeabilized in 10 mm Tris, 30 mm NaCl (TBS), pH 7.2, containing 10% normal goat serum (NGS) and 0.3% Triton X-100 for 1 hr. Primary antibodies were applied for 16 hr at room temperature (RT) in TBS containing 5% NGS and 0.3% Triton X-100. After washing in TBS, secondary antibodies were applied for 3 hr at RT. Sections were then rinsed with TBS, placed on slides (adult and P5 sections), placed under coverslips, and visualized with a scanning laser confocal microscope designed by Drs. Stephen J Smith and Noam Ziv (Stanford University, Stanford, CA).
Preparation of hippocampal neuron cultures. Embryonic hippocampal cell cultures were prepared from the hippocampi of 18- to 19-d-old fetal rats as described previously (Banker and Cowan, 1977;Fletcher et al., 1991). Hippocampi were treated with 0.05% trypsin and 0.53 mm EDTA for 15 min at 37°C, and cells were dissociated by triturating with a silicon-coated fire-polished pipette. Dissociated cells were plated at ∼5000 cells/cm2in neuronal medium [Earle’s MEM containing: glucose (6 mg/ml), apo-transferrin (100 μg/ml), ovalbumin (0.1%), NaPyruvate (1 mm), putrescine (100 μm), insulin (5 μg/ml), progesterone (20 nm), and selenium dioxide (30 nm)] supplemented with 10% equine serum (HyClone, Logan, UT). These cells were then allowed to attach to poly-l-lysine-coated coverslips for 2–6 hr, after which the coverslips were placed in cultures of previously prepared astroglia in neuronal medium. Neurons were fed once every 7 d. In some experiments, cultures were prepared from the hippocampi of 3-d-old postnatal rats as described previously (Malgaroli et al., 1995).
Immunocytochemistry of cultured cells. Cells were fixed by one of three methods. Some cultures were submerged in 4% PF and 120 mm sucrose in PBS for 20 min, extracted in −20°C methanol for 6 min, dehydrated, and rehydrated in 0.1 mglycine in PBS. In some experiments, the PF or methanol step was omitted. The best method of fixation varied with the antibody used and was adjusted appropriately. Cells were probed with a variety of antibodies diluted in PBS containing 0.4% saponin–2% NGS and 1% bovine serum albumin in PBS. The 9H5 monoclonal antibody was used for sec6 labeling (Kee et al., 1997). The 2E12 monoclonal antibody was used for sec8 labeling (Hsu et al., 1998). An affinity purified rabbit polyclonal antibody directed against bovine brain synapsin1 (1a and 1b) was purchased from Chemicon (Temecula, CA). A rabbit polyclonal antibody raised against bovine brain MAP2 was purchased from Biogenesis (Sandown, NH). The rabbit polyclonal antibody to synaptotagmin was made by Ken Miller (Stanford University) and was described in Jacobsson et al. (1994). After incubation with primary antibodies for either 1 hr at RT or overnight at 4°C, the cells were rinsed three times for 5 min in PBS and incubated with secondary antibodies for 1 hr at RT. Secondary antibodies were purchased from Jackson ImmunoResearch (West Grove, PA) and included dichlorotriazinyl amino fluorescein (DTAF)-conjugated AffiniPure goat anti-mouse IgG, Texas Red-conjugated AffiniPure donkey anti-rabbit IgG, and Cy5-conjugated AffiniPure goat anti-mouse IgG. Finally, cells were washed three times for 5 min, mounted onto slides, and visualized using either a Zeiss (Oberkochen, Germany) Axiophot or scanning laser confocal microscope.
Functional labeling of presynaptic axon terminals with FM1–43 and retrospective immunocytochemistry. FM1–43 loading was performed essentially as described by Ryan and Smith (1995). Coverslips with 8–9 days in vitro (div) embryonic hippocampal neurons were mounted in microscope chambers using vacuum grease and fitted with electrodes. After mounting onto the microscope, cultured neurons were constantly superfused at 34°C with a solution of 119 mm NaCl, 2.5 mm KCl, 2 mmCaCl2, 2 mm MgCl2, and 25 mm HEPES, pH 7.4, containing 50 μmd-2-amino-5-phosphonovaleric acid and 10 μm6-cyano-7-nitroquinoxaline-2,3-dione. Neurons were stimulated in the presence of 15 μm FM1–43 (Molecular Probes, Eugene, Oregon) with 300 field pulses of 30 mA at 10 Hz and then allowed to endocytose the dye for 30 sec. After 15–20 min of washing with dye-free superfusion solution, confocal images were obtained using custom multisite software (Drs. Noam Ziv and Stephen J Smith). FM1–43 was then unloaded from vesicles by stimulation in the absence of the dye. After unloading, the neurons were imaged again and then immediately fixed and labeled as described above. The same fields were then imaged for immunofluorescence and compared with the signal collected from the FM1–43 images.
Quantitative analyses methods. Cultures of different ages labeled with antibodies to synapsin1 and sec6 were used for quantification of the colocalization of sec6 and synapsin1. Synapsin1-positive sites were counted and scored for the presence of sec6 immunofluorescence by visualizing 10–20 fields containing cell bodies at each age through the 40× objective of a Zeiss Axiophot microscope. At least 1000 synapsin1 sites were counted for each age. Each field was quantified and averaged as shown in Figure 7. Alternatively, confocal images were obtained at the same days in vitro and >15 fields were analyzed at each age for colocalization using the Metamorph program (Universal Imaging Corporation, West Chester, PA). The Metamorph colocalization program is expected to give conservative estimates of colocalization for two reasons. (1) Maximal levels will be less because the sec6/8 complex and synapsin1 do not overlap exactly (see Figs. 4, 5); thus, the colocalization will never be 100%. (2) The Metamorph program will include dendritic contributions to sec6 immunofluorescence (see Fig.6L); thus, at later ages, the colocalization will be greater. These two predictions were borne out in Figure 7 in which the colocalization decreases from ∼80 to 40%. Nevertheless, this unbiased automated method substantiated the results obtained by counting, thus confirming the trend of less colocalization with age. The time course of decrease of colocalization with age was similar using the two quantification techniques; both showed a half-maximal colocalization at ∼7–8 div.
Colocalization analysis of FM1–43, synapsin1, and sec6 fluorescence was also performed using the Metamorph program and is presented in Tables 1,2. A total of 300 sec6 sites and 80 FM1–43 sites, which both loaded and unloaded, were counted.
A histogram of the frequency distribution of distances between sec6/8 puncta was accomplished using the VIEW program (written by Drs. Noam Ziv and Stephen J Smith) (data not shown). The average distance was calculated from this distribution.
Reagents. Unless otherwise stated, all reagents were obtained from Sigma (St. Louis, MO) or Life Technologies (Grand Island, NY).
RESULTS
sec6 expression is abundant in regions of the cerebral cortex undergoing synaptogenesis
To determine whether the sec6/8 complex plays a role in polarized neurite outgrowth and/or synaptogenesis during development of the cerebral cortex, brains from rats of different ages were sectioned and labeled with antibodies to sec6, synaptotagmin, and/or synapsin1. At all ages, similar results were obtained with synaptotagmin and synapsin1 (data not shown). Because sec6 and sec8 are stable components of the sec6/8 complex (Hsu et al., 1996), either sec6 or sec8 antibodies were used to analyze its distribution. In fetal brains, synaptogenesis is confined to regions of the developing cortex, termed the subplate, and the marginal layer (Chun and Shatz, 1988, 1989). In sections of brain from E18 rats, high levels of sec6 immunoreactivity were restricted to the subplate layer and the marginal layer (Fig.1A). These two layers were also specifically labeled by antibodies to synaptotagmin (Fig. 1B).
Soon after birth, synaptogenesis occurs throughout the cortex. Indeed, synaptotagmin and sec6 immunofluorescence were broadly distributed throughout the cortex of P5 rat brains (Fig.1D,E). Although the intensity of synaptotagmin labeling is low at P5, it is clearly above an IgG background, which has been subtracted from the images shown. The correlated change in sec6 and synaptotagmin labeling from E18 to P5 suggests that the sec6/8 complex is located at sites of developing synapses. Interestingly, the intensity of sec6 labeling was greatly decreased in adult compared with P5 animals (Fig.1E,G) whereas the intensity of synaptotagmin labeling was increased (Fig.1D,F), suggesting that the sec6/8 complex may either be greatly reduced in its abundance and therefore not required for mature neuronal function or modified and not recognized by the antibody. The presence of high levels of sec6/8 complex in brain regions undergoing synaptic development suggests a role for the sec6/8 complex in neurite outgrowth and synaptogenesis.
The sec6/8 complex is located in the terminals of growing neurites and in periodic domains of axons
The subcellular distribution of the sec6/8 complex in neurons was analyzed to determine whether it plays a role in the development of neuronal polarity and/or synaptic structures. Primary cultures of embryonic hippocampal neurons provide a useful system in which to study these phenomena. These cells exhibit polarized axonal and dendritic domains regardless of contact with other cells and can be grown separately from glia, making visualization of fine processes possible (Banker and Cowan, 1977; Fletcher et al., 1991). Furthermore, as neurons mature and contact each other, they develop functional synapses (Bartlett and Banker, 1984). Neurons at various stages of development were decorated with antibodies directed against sec6 and sec8 to discern where the sec6/8 complex was distributed with respect to active vesicle exocytosis.
At 2 div, neurons that have not yet formed synapses (Fletcher et al., 1991) exhibited intense sec6 labeling of the cell body, dendritic growth cones, axonal branch points, and axonal growth cones (Fig.2A,B). Labeling of the cell body probably represented a soluble pool of the complex before its targeting to the plasma membrane. The six shorter processes with sec6 at their terminal growth cones in Figure2B are likely immature dendrites (Dotti and Banker, 1987). This pattern of sec6/8 complex labeling is consistent with a role in targeting of vesicles to sites of exocytosis in developing neurons, such as growth cones.
Interestingly, sec6 (Fig. 2B) and sec8 immunofluorescence (Fig. 2D) were observed along axons in a periodic pattern, indicating that the sec6/8 complex was located in discrete domains along the axon. The average distance between these domains was 3.2 ± 1.1 μm. Labeling with antibodies to syntaxin1 (Fig.3A,C), β-catenin (data not shown), and the septin CDC10 protein (Hsu et al., 1998) using identical fixation and immunocytochemical techniques did not reveal a similar pattern of periodic staining, ruling out the possibility of fixation and/or labeling artifacts. These domains were further characterized by double labeling with antibodies to sec6 and synaptotagmin, a vesicle marker. Fields containing single axons were selected and visualized at high magnification. The sec6 staining was located peripherally in a “shell” around the vesicle marker (Fig.4A,B), suggesting that the periodic discrete domains of sec6 were present only on the plasma membrane. This plasma membrane labeling is consistent with previous biochemical experiments, which demonstrated the existence of a pool of the sec6/8 complex bound to the plasma membrane (Hsu et al., 1996). Filopodia originating from both the growth cone and the axon also contained punctate sec6 immunofluorescence (Fig.4B–D). All areas of sec6/8 complex labeling are likely locations of membrane trafficking activity in growing axons.
Older cultures (6–9 div) were double-labeled with antibodies to MAP2 (a dendritic marker) and sec6 to determine whether the sec6/8 complex is present in dendrites, as well as axons. Although some lighter, diffuse sec6 labeling was observed in dendrites and the cell body (Figs. 5,6H), more intense sec6 staining was found predominantly in MAP2-negative axons (data not shown). The diffuse dendritic and cell body labeling could represent the soluble pool reported previously (Hsu et al., 1996).
The sec6/8 complex marks sites along axons that can become synapses
The discrete labeling pattern of the sec6/8 complex in the axons of very young neurons suggests that it may be a molecular spatial landmark for vesicle delivery to nascent presynaptic specializations. To investigate this idea, cultures were labeled with antibodies directed against sec6 and synapsin1 at 6 div, a time when many initial contacts are forming between presynaptic and postsynaptic neurons (Fletcher et al., 1991). We used the presence of focal points of synapsin1 immunofluorescence as a marker for synapses (Bartlett and Banker, 1984; Fletcher et al., 1991; Ryan et al., 1993). Many axons were found growing around cell bodies and dendrites, likely establishing the initial stages of synapse formation (Fig.5A–C). sec6 was distributed in a periodic manner in these axons (Fig. 5B). In axonal regions labeled by sec6 antibodies, many, but not all, of the sec6 domains also contained synapsin1 immunofluorescence (Fig.5A,C). In these regions, synapsin1 labeling was not observed in between, but only coincident with, the periodic sec6 labeling along axons, suggesting that sec6/8 complex sites are synaptic precursors.
Unexpectedly, many axonal regions containing synapsin1-immunoreactive synapses did not contain sec6 labeling. These regions likely contain mature synapses devoid of the sec6/8 complex because they are observed apposed to dendrites (Nomarski image not shown). Synapsin1-positive sec6-negative regions were observed along entire axons (Fig.6L), suggesting that the axonal regions imaged were in different developmental stages. The observations that, in younger axonal processes (3 div), synapsin1 was not found in the absence of sec6 and that a high number of sec6 labeled axons were present indicate that synapsin1 does not accumulate in the absence of sec6 and that sec6 accumulation precedes that of synapsin1.
To investigate the relationship between sec6/8 complex labeled axonal domains and mature synapses, we studied the time course of sec6/synapsin1 coexpression in neuronal cultures of different ages. In young cultures (4 div), many axons were found growing around cell bodies and dendrites (Fig.6A,E,I). sec6 was distributed in the typical periodic manner in these axons. Although a small percentage of the sec6 labeled axonal domains contained faint synapsin1 staining, the sites of axodendritic contact contained intense synapsin1 labeling (Nomarski image not shown). At older stages of development (6–12 div), more synapsin1 sites were observed (Fig. 6B–D), with decreased colocalization with sec6 (Fig. 6J–L). At 12 div, many synapsin1 labeled sites without sec6 staining were present in axons that run along diffusely sec6-labeled dendrites (Fig. 6L). Some axons at 12 div still contained labeling of sec6 but not of synapsin1 (Fig. 6L, left), likely representing axons that had not yet contacted dendrites. These results suggest that the sec6/8 complex is present in the presynaptic component of newly formed, but not mature, synapses.
To more rigorously determine the relationship between synapsin1 and sec6, immunofluorescence was quantified at different developmental ages. A large number of fields (see Materials and Methods) were imaged using either conventional or scanning laser confocal microscopy in each of several different labeled preparations of hippocampal cultures. Synapsin1-immunoreactive sites were counted at low magnification and scored for the presence or absence of sec6 immunofluorescence. Colocalization decreased from ∼100 to 20% between 3 and 12 div (Fig. 7, solid line). Similar results were observed using a less precise, automated method (Fig. 7, dashed line) (see Materials and Methods for details). Colocalization of the sec6 immunoreactivity in synapsin1 sites remained at ∼20% later in culture because axons were continually growing in embryonic hippocampal cultures and synaptogenesis occurs at both early times and later ages (Fletcher et al., 1994). These data support the hypothesis that the sec6/8 complex tags regions of the plasma membrane for potential delivery of synaptic vesicles but is downregulated in mature synapses.
The sec6/8 complex is not required for functional local cycling of synaptic vesicles
Mature synapses are characterized by specialized local vesicle cycling in the presynaptic region, where vesicles are repeatedly exocytosed and endocytosed (Ryan and Smith, 1995). To test whether synapsin1 and/or sec6 sites support functional vesicle cycling, we monitored vesicle recycling with the vital dye FM1–43 (Ryan and Smith, 1995; Betz et al., 1996). Cultures, aged 8–9 div were stimulated with field electrodes in the presence of Ca2+ and FM1–43 and then washed for 20 min and imaged. Cells were then stimulated in the absence of FM1–43 to unload the endocytosed dye. After imaging, cells were fixed and labeled with antibodies to sec6 and synapsin1, and the same cell fields were imaged for immunofluorescence. The three fluorescence signals were compared for each FM1–43-, sec6-, or synapsin1-positive site.
We quantified the incidence of colocalization between sec6, synapsin1, and FM1–43 (Tables 1, 2). At this intermediate time during synaptogenesis, we expected to observe presynaptic specializations in a variety of stages of maturity. As shown in Figure8, sites at which FM1–43 was taken up through endocytosis were usually labeled by the synapsin1 antibody (>82%). sec6-positive sites were scored for the presence of FM1–43 and/or synapsin1 (Table 1). Sixty-six percent of sec6 sites did not contain either FM1–43 or synapsin1 (Fig. 8, 1), indicating that most regions containing the sec6/8 complex are not functional synapses. Exocytosis of vesicles may still occur at these synapsin1-negative locations, but these vesicles would not be detected using FM1–43, which only detects locally confined clusters of vesicles undergoing cycles of exocytosis and endocytosis. In fact, only 4% of sec6 sites contained FM1–43 in the absence of synapsin1; these likely fall within experimental error of the fixation–immunostaining technique. Fourteen percent of sec6 sites contained synapsin1 but not FM1–43 (Fig. 8, 2). These may represent newly formed nonfunctional synapses. Sixteen percent of sec6 sites contained both synapsin1 and FM1–43 (Fig. 8, 3), indicating that the sec6/8 complex can be present in functional synapses.
To investigate the significance of the sec6/8 complex in mature synapses, functional synapses were scored for the presence of the sec6/8 complex (Table 2). Only 33% of synapsin1–FM1–43 sites contained sec6 labeling (Fig. 8, 4), confirming that the sec6/8 complex is not required or is modified in functioning synapses. Synapses containing sec6, synapsin1, and FM1–43 may represent immature synapses because the majority of FM1–43/synapsin1 sites do not contain sec6. These results are consistent with the hypothesis that the sec6/8 complex marks axonal locations that have the capacity to become synapses. As sites mature, the sec6/8 complex is no longer required, and vesicles will cycle locally in the absence of the sec6/8 complex.
DISCUSSION
Previous studies have promoted the hypothesis that the sec6/8 complex plays a role in specifying sites of exocytosis important for polarized secretion in yeast and MDCK cells. Such a role likely extends to neurons, highly polarized cells where targeting mechanisms are crucial for organized membrane trafficking. We have tested this hypothesis by analyzing the distribution of the mammalian sec6/8 complex in neural tissue and cultured neurons during various stages of development of polarity and synaptogenesis. Our results suggest that the sec6/8 complex defines domains of membrane addition and synaptogenesis in growing axons.
Exactly where vesicles fuse with axonal plasma membrane in developing neurons is ambiguous. Conflicting reports have implicated either the cell body or the terminal growth cone as the important site of vesicle addition for axonal growth (Popov et al., 1993; Craig et al., 1995). It is also possible, in the hippocampal culture system, that membrane addition can occur along the axon, as well as in growth cones (Futerman and Banker, 1996). Additionally, Golgi-derived immature synaptic vesicles may fuse at multiple sites along the axon as they travel toward their ultimate synaptic destination (Nakata et al., 1998). These processes may require machinery for vesicle fusion along the plasma membrane. Thus, it is possible that the sec6/8 complex is required along growing axons to mediate targeted exocytosis of constitutive and synaptic vesicles.
The results presented here provide the first description of a set of proteins that demarcates domains of the neuronal plasma membrane as sites of possible vesicle exocytosis underlying the development of presynaptic specializations. The sec6/8 complex was observed in periodic axonal domains in cultured hippocampal neurons, reminiscent of previously observed periodic synaptic vesicle exocytosis domains. These periodic regions of potential exocytosis in axons that have not contacted target cells have been described in embryonic hippocampal cultures (Matteoli et al., 1992), dorsal root ganglion neurons (Nakata et al., 1998), and in developing cortical neurons in brain (although these fetal neurons may have postsynaptic partners) (Chun and Shatz, 1989). The periodic distribution of the sec6/8 complex may ensure an appropriate nonoverlapping distribution of synapses in adult neurons. Because the arrival of the sec6/8 complex precedes the appearance of synaptic vesicle clusters, we propose that the sec6/8 complex signals the accumulation of components of the presynaptic terminal at predetermined sites along axons. This may be achieved via the targeting of vesicles containing presynaptic plasma membrane proteins. Probably only a fraction of sec6/8 sites become synapses because they did not always colocalize with vesicle markers or functional vesicle cycling. Other molecules may be required for deciding at which sec6/8 sites vesicles will accumulate in the process of synaptogenesis. Perhaps there are also negative signals that prevent such accumulation in areas immediately surrounding the domains demarcated by the sec6/8 complex. Thus, the sec6/8 complex may be part of a signaling pathway in developing axons important for organizing the compartmentalization of components necessary for presynaptic functioning.
The distribution of the sec6/8 complex is interesting in the context of previous studies in hippocampal cultures, which have demonstrated that parts of the presynaptic specialization are organized early, before functional synapses are formed. Axons have been shown to be competent to rapidly form synapses, suggesting that the presynaptic components are organized before contacts with postsynaptic cells are established (Fletcher et al., 1994). This idea is supported by electron microscopy and live-imaging experiments, which have demonstrated the presence of nonsynaptic vesicle clusters in axons. These clustered vesicles can undergo cycling at the plasma membrane in response to activity and can move in bulk throughout the axon in both anterograde and retrograde directions (Matteoli et al., 1992; Kraszewski et al., 1995; Dai and Peng, 1996; Nakata et al., 1998), indicating that vesicles are capable of accumulating in axons in the absence of contacts with other cells but that contact with a dendrite is necessary for stabilization of a vesicle cluster at a synapse (Kraszewski et al., 1995; Dai and Peng, 1996). The distribution of the sec6/8 complex in axons and filopodia suggest that it may be important for clustering mobile vesicle pools at sites of axodendritic contacts.
The data presented here in neurons is redolent of the observations in yeast and MDCK cells in which the sec6/8 complex is located at sites of and required for polarized secretion (TerBush and Novick, 1995; Finger et al., 1998; Grindstaff et al., 1998) (Fig.9A,B) . One obvious difference between the present and previous data is the downregulation observed in differentiated neurons, which is not seen in polarized MDCK cell monolayers. Polarized MDCK cells are not terminally differentiated but, instead, are continually testing their intercellular connections for retention of polarity as evidenced by the rapid turnover of E-cadherin (5 hr) (Shore and Nelson, 1991). A steady supply of the sec6/8 complex is therefore probably required for targeted exocytosis. The epitope recognized by the sec6 antibody may be modified or occluded by other proteins during synapse development. Alternatively, in mature synapses, the sec6/8 complex may not be needed because the large scale recruitment of vesicles to the synapse no longer occurs. Synaptic vesicles in mature synapses may be able to retain their molecular components, with minimal contribution from the cell body. However, the sec6/8 complex may still be required for neuronal function in adult brain, although its immunoreactivity, and probably abundance, is greatly reduced. For example, the sec6/8 complex may be required for the trafficking of vesicles to new synapses and, as a result, may be present in those cells that sprout new axon terminals or are undergoing axonal growth as a mechanism of synaptic plasticity. A low level of the sec6/8 complex may also be required for the constitutive secretion of Golgi-derived vesicles serving homeostatic functions in neurons. Thus, the sec6/8 complex may be important for general secretion mechanisms used by all cells, and it may have been adapted to serve neuron-specific functions.
In the context of these data, we propose a model of the role for the sec6/8 complex in vesicle targeting in developing neurons (Fig.9C). In very young neurons, the sec6/8 complex is present in the growth cones of all processes extending from the cell body. The sec6/8 complex is also clustered in periodic regions along the length of the developing axon. Eventually, immature synaptic vesicles and associated proteins (synaptotagmin, synapsin1, etc.) are clustered in some sec6/8 complex-containing domains. Once an axon contacts a dendrite (Ziv and Smith, 1996), the synapse is stabilized, leading to downregulation of the sec6/8 complex. A pool of mature synaptic vesicles is left behind at presynaptic active zones. It is possible that the need for the sec6/8 complex is obviated by postsynaptic signals. At this stage in culture, the distal tip of the axon may still be growing and forming synapses, thus preserving the need for the sec6/8 complex in the axon in addition to a possible role in constitutive secretion. Furthermore, a diffuse pool of the sec6/8 complex remains in the cell body, the dendrites, and perhaps axons directing constitutive secretion.
An important future topic of research will be the description of the molecular mechanisms underlying the targeting and localization of the sec6/8 complex to potential presynaptic sites. If, as proposed, the sec6/8 complex is involved in establishing potential active zones for synaptic vesicle docking and fusion, it may be possible to use the proteins of the complex as molecular handles with which to characterize other molecules involved in axonal differentiation and synapse formation. The activation of the sec6/8 complex in response to experience in adult brain may result in the formation of new synapses. One prediction is that the sec6/8 complex would rapidly respond to molecules that signal either stabilization or modification of synapses. Such a regulatory switch would, through the sec6/8 complex, redirect membrane flow in nerve terminals from constitutive to local recycling (Xie and Poo, 1986; Zoran et al., 1991). Identification of these sec6/8 complex interacting proteins will provide important insights into the biochemical basis of neural circuitry development and plasticity.
Footnotes
We thank Drs. Svend Davanger and Erika Piedras-Renteria for assistance with hippocampal neuron cultures and experimental techniques; Drs. Susan McConnell and Alex Zhang for aid obtaining and analyzing brain section data; Dr. Charles F. Stevens for discussions; Dr. Jack Waters for help with FM1–43 experiments; Drs. Stephen J Smith, Cindy Adams, Jamie Jontes, and Susanne Ahmari for benefaction with confocal microscopy and discussion; and Drs. Cindy Adams, Richard Lin, Eva Ogielska, Rytis Prekeris, and Martin Steegmaier for critical reading of this manuscript.
Correspondence should be addressed to Dr. Richard H. Scheller at the above address.