SNARE proteins (soluble NSF‐attachment protein receptors) are thought to be central components of the exocytotic mechanism in neurosecretory cells, but their precise function remained unclear. Here, we show that each of the vesicle‐associated SNARE proteins (v‐SNARE) of a chromaffin granule, synaptobrevin II or cellubrevin, is sufficient to support Ca2+‐dependent exocytosis and to establish a pool of primed, readily releasable vesicles. In the absence of both proteins, secretion is abolished, without affecting biogenesis or docking of granules indicating that v‐SNAREs are absolutely required for granule exocytosis. We find that synaptobrevin II and cellubrevin differentially control the pool of readily releasable vesicles and show that the v‐SNARE's amino terminus regulates the vesicle's primed state. We demonstrate that dynamics of fusion pore dilation are regulated by v‐SNAREs, indicating their action throughout exocytosis from priming to fusion of vesicles.
Neuronal SNAREs (soluble NSF‐attachment protein receptors) include synaptobrevin, which resides on vesicles and the plasma membrane proteins, syntaxin and SNAP‐25 (Chen and Scheller, 2001; Jahn et al, 2003). At synapses, null mutants of any of the three SNARE proteins exhibit a strong inhibition of action potential‐evoked transmitter release (Schulze et al, 1995; Deitcher et al, 1998; Schoch et al, 2001; Washbourne et al, 2002), an observation that agrees well with the finding that these proteins are specifically targeted by clostridial neurotoxins, which are potent inhibitors of neurotransmitter release. Morphological evidence showed that docking of secretory vesicles at the plasma membrane is not impaired after genetic ablation or proteolysis of SNARE proteins, implicating a ‘postdocking’ role of these proteins in the exocytotic pathway (Hunt et al, 1994; Broadie et al, 1995). Recent studies on SNAP‐25 in chromaffin cells using either single amino‐acid substitutions, site‐specific antibodies or expression of splice variants in knockout cells suggest that the function of this protein provides the molecular basis for ‘priming’ of secretory vesicles, a reaction that transfers morphologically docked vesicles into an exocytosis‐competent state (Xu et al, 1999; Wei et al, 2000; Sorensen et al, 2003; Nagy et al, 2004). Still, neither SNAP‐25 deficiency nor the lack of synaptobrevin II abolishes spontaneously occurring vesicle fusion or secretion when a long‐lasting Ca2+ stimulus is applied, raising the question of whether remaining exocytosis occurs with the help of an alternative SNARE complex or by a SNARE‐independent mechanism (Yoshihara et al, 1999; Schoch et al, 2001; Washbourne et al, 2002; Sorensen et al, 2003). Furthermore, data from other systems have indicated that SNAREs may act before fusion and are not directly involved in executing fusion (Tahara et al, 1998; Ungermann et al, 1998).
To gain new insight into the mode of SNARE function in exocytosis, we examined alternative v‐SNAREs in the same exocytotic pathway. In following this strategy, we analyzed how structurally homologous v‐SNAREs of a chromaffin granule, synaptobrevin II (sybII) and cellubrevin (ceb, also referred to as VAMP 2 and VAMP 3, respectively), contribute to catecholamine secretion from chromaffin cells (Baumert et al, 1989; Elferink et al, 1989; McMahon et al, 1993). Ceb shares a high degree of similarity with sybII, is expressed in a wide variety of tissues and is also a substrate for the proteolytic action of tetanus toxin (McMahon et al, 1993; Galli et al, 1994). Previous studies identified ceb on secretory vesicles of neuroendocrine cells (Chilcote et al, 1995) and glia cells (Bezzi et al, 2004) but also implicated the protein in the fusion of endosome‐derived, transferrin receptor‐containing vesicles that undergo exocytosis constitutively and in a Ca2+‐independent manner (Galli et al, 1994). To study the functional impact of these v‐SNARE proteins in Ca2+‐triggered exocytosis, we took advantage of recently developed mouse strains, being deficient either for sybII (Schoch et al, 2001) or for ceb (Yang et al, 2001) and, in addition, generated a new double v‐SNARE null mouse.
Our experiments demonstrate that secretion is abolished only in the absence of both sybII and ceb, without affecting biogenesis or docking of granules, indicating that one of these v‐SNAREs is absolutely required for Ca2+‐dependent granule exocytosis. We provide evidence that sybII is the major, if not the only, v‐SNARE acting in wild‐type cells, but is efficiently substituted by ceb in sybII knockouts (ko), suggesting that v‐SNAREs act promiscuously in genetically deficient but specifically in wild‐type cells. Furthermore, membrane capacitance measurements and carbon fiber amperometry are used to elucidate how the individual v‐SNARE proteins regulate Ca2+‐triggered stimulus–secretion coupling and exocytotic membrane merger.
Granule exocytosis in isolated chromaffin cells was synchronized using flash photolysis of caged Ca2+ (NP‐EGTA), and changes in the intracellular calcium concentration ([Ca]i) were measured with a combination of calcium indicators (Fura‐2 and Furaptra). Photolytic ‘uncaging’ of Ca2+ leads to a step‐like increase in [Ca]i that stimulates granule exocytosis, which is detected by measuring the membrane capacitance at high time resolution (Figure 1). The secretory response of a wild‐type chromaffin cell to such a stimulus can be roughly divided into two kinetically distinct phases (Heinemann et al, 1994; Voets et al, 1999): an initial phase (also referred to as exocytotic burst), reflecting the exocytosis of granules from a release‐ready state and a subsequent sustained phase that is thought to represent refilling of the just emptied pool by recruitment of new vesicles into the exocytosis‐competent state (‘priming’). At high [Ca]i, priming is immediately followed by fusion producing a sustained increase in membrane capacitance. At resting levels of [Ca]i, the balance between ‘forward‐directed’ priming and ‘backward‐directed’ depriming reactions should determine the pool size of release‐ready organelles (Voets, 2000; Rettig and Neher, 2002).
Synaptobrevin II deficiency versus cellubrevin deficiency
In the absence of synaptobrevin II (sybII ko), Ca2+‐triggered secretion from chromaffin cells is only moderately diminished (Figure 1A). This finding was unexpected considering the observation that poisoning of wild‐type cells with tetanus toxin (TeNT) leads to a complete loss of exocytosis (Xu et al, 1998). Indeed, expression of TeNT in sybII ko cells abolishes secretion, showing that an alternative toxin substrate, most likely ceb, mediates sybII‐independent exocytosis. The analysis of wild‐type and mutant cells reveals that loss of sybII diminishes the exocytotic burst size (Figure 1B). Both components of the exocytotic burst, the fast phase (RRP, readily releasable pool) and the slow phase (SRP, slowly releasable pool), are similarly affected, but no corresponding change in the sustained phase of the exocytotic response is observed. Thus, lack of sybII facilitates depriming of the vesicles leading to the observed reduction of RRP and SRP size. In contrast, the kinetic rates of the exocytotic burst (τRRP, τSRP; Figure 1B) and the delay between flash and onset of the response (wt: 4.4±0.77 ms; sybII ko: 5.01±0.5 ms) remain unchanged, showing that the alternative v‐SNARE component enables bona fide Ca2+‐triggered exocytosis. The same effects are measured for a second flash (given with a 2 min interval), indicating that differences in ‘depriming’ of wild‐type and sybII ko granules are robust and remain even after strong stimulation of exocytosis.
Astonishingly, lack of cellubrevin (ceb ko) has no profound effect on secretion (Figure 1C and D), neither the first nor the second flash response shows significant alterations compared with controls. Therefore, sybII is either sufficient or can readily compensate for the lack of ceb in the exocytotic mechanism. To address this issue further, we determined the expression levels of sybII and ceb on the background of the different v‐SNARE knockout phenotypes in cultured chromaffin cells (Supplementary Figure A and B). The data show that, in the absence of sybII, ceb's expression level is significantly upregulated, on average by 36%. Similarly, the mean immunosignal tlsbfor sybII is increased by about 27% when ceb is absent. These observations are compatible with the view that sybII and ceb are functionally interchangeable and can act in the same exocytotic pathway.
Double v‐SNARE deficiency
To test whether cellubrevin mediates secretion in sybII ko cells, we generated a mouse strain that is deficient for both proteins (double v‐SNARE null mouse, dko; see Materials and methods). In fact, Ca2+‐evoked secretion from dko cells is nearly abolished (Figure 2A). The flash‐evoked response from these mutant cells exhibits no significant exocytotic burst (less than 7% of control measured at 0.5 s after stimulation). This result suggests that each of the two v‐SNAREs is sufficient to establish a standing pool of release‐ready organelles. In close correlation, strong immunoreactive bands for both, sybII and ceb are observed with Western blots of wild‐type adrenal gland homogenate prepared at embryonic stage E18.5 (Figure 2C). Furthermore, TI‐VAMP (toxin‐insensitive VAMP; Coco et al, 1999) but not synaptobrevin I, the other known TeNT substrate, was detectable on immunoblots. Treatment of dko cells with TeNT led to no further reduction of the signal (Figure 2A), implicating TeNT‐insensitive VAMPs like TI‐VAMP or VAMP 8 (Paumet et al, 2000) in mediating the small remaining response and excluding synaptobrevin I that may be expressed below the detection limits of the immunoblot analysis. Western blot analysis of adrenal gland and of brain homogenate furthermore reveals that double v‐SNARE deficiency causes no compensatory changes in the expression levels of other synaptic proteins (Figure 2D and E).
Using electron microscopy, we investigated whether removal of the two v‐SNAREs affects number, size or spatial distribution of chromaffin granules (Figure 3A). dko cells exhibit the same density of vesicles as observed in controls (wt: 2.9±0.2 vesicles/μm2; dko: 3.1±0.3 vesicles/μm2), indicating that lack of the v‐SNAREs does not interfere with the de novo synthesis of the secretory organelles (Figure 3B). The size distribution of double v‐SNARE‐deficient vesicles closely resembles that observed for wild‐type vesicles (vesicle radius: wt: 65±18 nm; ceb ko: 66±16; dko: 66±15 nm; Figure 3C) and measurement of the granule‐to‐plasma membrane distance revealed neither significant changes in the number of morphologically docked vesicles (<50 nm) nor in the overall spatial distribution of the granules (Figure 3D). Thus, sybII and ceb are not required for biogenesis and docking of secretory organelles in chromaffin cells.
v‐SNARE deficiencies with other stimuli
The distinct functional consequences of the v‐SNARE deficiencies are similarly evident for a physiological stimulus of granule exocytosis (Figure 4A–C). Exocytosis triggered by a train of depolarizations is reduced in sybII ko cells, unchanged in ceb ko cells and almost abolished in dko cells. This finding holds for the first capacitance response (within the stimulus train; Figure 4D), which mainly reflects exocytosis of release‐ready vesicles (Voets et al, 1999). In contrast, amplitudes of the corresponding depolarization‐induced Ca2+ currents are unaffected in all studied genotypes. Thus, granule exocytosis triggered by Ca2+ influx through voltage‐gated Ca2+ channels exhibits the same dependence on the different v‐SNARE proteins as observed with photolytic ‘uncaging’ of Ca2+, putting no constraints on a preferred use of sybII during depolarizing stimuli, as one might expect from the strong inhibition of depolarization‐induced release in sybII ko neurons (Schoch et al, 2001).
To study whether changes in the capacitance response observed for the different knockout phenotypes mirror indeed alterations in granule exocytosis, we used amperometry to measure catecholamine secretion directly. Wild‐type cells respond to rapid application of high‐potassium‐containing solution with a strong increase in the frequency of amperometric spikes (48±3 events/application; Figure 4E). For dko cells, 10 out of 16 cells showed no exocytotic event with such a stimulus. On average, only 1±0.5 event/application is observed, corroborating the result that Ca2+‐triggered granule exocytosis is abolished in the absence of both v‐SNAREs (Figure 4H). A similarly strong block of exocytosis is found upon poisoning of wild‐type cells with TeNT (0.8±0.4 events/application, n=10, data not shown). Figure 4I plots the amplitude of the flash‐evoked capacitance response versus the mean number of amperometric spikes recorded for the different v‐SNARE deficiencies. The combined set of data reveals a linear relationship, suggesting that changes in the Ca2+‐triggered capacitance increase can be attributed to alterations in the frequency of granule exocytosis (r2=0.98). In contrast to other SNARE knockouts (Yoshihara et al, 1999; Schoch et al, 2001; Sorensen et al, 2003), a strong impairment of the release machinery in dko cells is also observed when a massive and long‐lasting Ca2+ stimulus is used (Supplementary Figure C). In these experiments, cells were perfused with high‐Ca2+‐containing solution (10 μM free [Ca2+]i) and secretion was examined simultaneously with amperometry and membrane capacitance measurements. dko cells did not show a significant increase in either membrane capacitance (4% of control) or frequency of amperometric signals (6% of control). Taken together, double v‐SNARE deficiency produces a nearly complete loss of Ca2+‐dependent granule exocytosis.
Expression of synaptobrevin II and cellubrevin restores secretion in dko cells
To test whether the observed effects are specific for the absence of the individual v‐SNAREs, we acutely overexpressed the proteins in dko cells using the Semliki forest virus system (Liljestrom and Garoff, 1991). Expression of sybII completely restores the flash‐evoked response of dko cells to the level found in ceb ko cells, the littermate control (Figure 5A). Thus, except for the lack of the v‐SNARE proteins, the release machinery remains intact in mutant cells, agreeing well with our biochemical and morphological results (Figures 2 and 3). A large amount of secretory activity is also regained by expression of ceb in dko cells resembling the sybII ko phenotype (Figure 1A). Evidently, the alternating expression of the individual v‐SNAREs in dko cells creates a mirror image of the single‐knockout phenotypes.
By measuring the change in protein levels upon overexpression in dko cells, we found that sybII and ceb levels increase on average more than 14‐fold compared with endogenous levels in wild‐type cells (Supplementary Figure A and B), indicating that molecular differences rather than different expression levels of the proteins determine the phenotypes. Consistent with this result, secretion from cells heterozygous for sybII, analyzed either with amperometry or with capacitance measurements, was indistinguishable from wild‐type responses (data not shown).
The cytoplasmic domains of sybII and ceb are nearly identical but exhibit one amino‐acid exchange A37N and a nonconserved amino terminus (aa 1–32, numbers refer to sybII; Figure 6A). To test whether these structural determinants regulate the vesicle's priming stability, we exchanged the amino‐terminal domains (aa 1–37) of the v‐SNAREs. Indeed, expression of the chimera protein Syb‐N (sybII N‐terminus+ceb) in dko cells (Figure 6B and C) supports a larger secretory response and a larger exocytotic burst than the Ceb‐N chimera (ceb N‐terminus+sybII). Notably, Syb‐N‐mediated exocytosis closely resembles the ceb ko response (Figure 6B, gray line). For Ceb‐N, the RRP and the SRP components are significantly reduced, whereas the kinetic rates of the exocytotic burst are unchanged. These results indicate that the amino‐terminal domain of the v‐SNARE protein controls the priming stability of chromaffin granules.
Synaptobrevin II promotes faster fusion pore expansion than cellubrevin
To determine whether the functional differences between sybII and ceb extend to the level of membrane merger, we took advantage of the high‐time resolution of amperometry (Figure 7A). For each amperometric spike, evoked by high‐K+ depolarization in wild‐type and single‐knockout cells, quantal size, amplitude and kinetic parameters were determined. As shown in Figure 7B and C, neither the amount of transmitter released from a granule nor the peak amplitude of the oxidative current spike changes in the absence of one of the v‐SNARE proteins. Exocytosis starts with the formation of a fusion pore that restricts initial transmitter efflux from the vesicle generating a ‘foot’ signal, which precedes the amperometric spike (Chow et al, 1992; Bruns and Jahn, 1995; Albillos et al, 1997; Figure 7A). This initial phase of release is significantly altered in the absence of sybII. Fusion events, recorded in sybII ko cells, exhibit a much longer ‘foot’ duration (Figure 7F–H) leading to an increase in charge and in maximum current amplitude of the ‘foot’ signal as expected for prolonged fusion pore expansion (Table I, mean of median values determined for each cell). In contrast, the kinetic properties of the main phase of transmitter discharge are unaffected (Figure 7D and E), rendering the possibility unlikely that experimental inconsistencies, such as variable cell‐electrode spacing, are responsible for the prolongation of the fusion pore signal. Thus, lack of sybII specifically delays the moment when the slow expansion of the fusion pore proceeds to a more rapid expansion mode (spike phase). In contrast, ‘foot’ signals recorded from ceb‐deficient cells are identical to those of wild‐type cells (Figure 7F–H), indicating that chromaffin granules equipped only with ceb fuse more slowly with the plasma membrane than sybII‐carrying granules. Expression of sybII in sybII ko cells fully restores the wild‐type phenotype (Figure 7G and H), whereas expression of ceb failed to accelerate fusion pore expansion. Therefore, not the number of v‐SNARE proteins, but their molecular properties determine the fusion pore dynamics. We conclude that v‐SNAREs act at a late stage of exocytosis regulating the timing of fusion pore dilation.
Functional redundancy of v‐SNAREs in Ca2+‐dependent granule exocytosis
In this study, we show that the presence of one of the v‐SNARE proteins, sybII or ceb, suffices chromaffin granules to perform bona fide Ca2+‐dependent exocytosis. The fidelity by which ceb promotes stimulus–secretion coupling was unexpected, considering that this protein is virtually undetectable in neurons, but it is in line with the high degree of sequence homology to sybII within the SNARE domain, which mediates the interaction with other SNARE partners (Sutton et al, 1998). This result, together with recent studies in yeast and Drosophila (Bhattacharya et al, 2002; Liu and Barlowe, 2002; Vilinsky et al, 2002), suggests functional redundancy among SNARE proteins as a more widespread phenomenon than expected from the hypothesis that these proteins encode for compartmental specificity in intracellular membrane transport (McNew et al, 2000). For example, experiments in yeast have shown that Ykt6p, a v‐SNARE protein functioning at late stages of the secretory pathway, compensates for the lack of Sec22p, which is required for ER–Golgi transport (Liu and Barlowe, 2002). The ubiquitously expressed Drosophila v‐SNARE syb, which might be comparable with ceb, is able to substitute, at least upon strong overexpression, for the neuronal isoform (n‐Syb) in n‐Syb nulls by supporting some evoked exocytosis at the neuromuscular junction (Bhattacharya et al, 2002). Our experiments in chromaffin cells, using high‐resolution membrane capacitance measurements together with a well‐defined Ca2+ stimulus, extend these findings. Particularly, ceb's property to support a standing pool of release‐ready organelles with unchanged stimulus–secretion coupling identifies this protein as a true functionally redundant v‐SNARE for rapid Ca2+‐triggered exocytosis. Still, our results also provide evidence that sybII is the preferred, if not the only, v‐SNARE acting in the secretion of wild‐type chromaffin cells. First, lack of sybII attenuates secretion and, furthermore, its overexpression (but not of ceb) in double v‐SNARE‐deficient cells rescues the exocytotic response to wild‐type levels showing that sybII is required and functionally sufficient as cognate v‐SNARE. Second, ceb supports exocytosis only with reduced efficiency, but its removal causes no increase in secretion, as expected if both proteins would compete in the exocytotic mechanism. One might speculate that secretion has reached an upper limit under wild‐type conditions preventing any further increase of the response upon removal of ceb. However, overexpression of ceb in wild‐type cells produces no reduction of the secretory response (Supplementary Figure E), reinforcing the view that ceb does not compete with sybII in the exocytosis of wild‐type cells. Taken together, these results suggest that ceb plays a minor, if any, role in granule exocytosis of wild‐type cells, but efficiently substitutes for sybII in its absence. The different contribution of ceb to secretion from sybII ko and wild‐type cells suggests a precise control that functionally segregates the individual v‐SNARE components in the full context of the protein machinery but fails under genetically deficient conditions. Most likely, structures outside of the highly homologous SNARE domain encode for the preferential use of sybII. Its long, nonconserved amino terminus is well suited to confer specificity and to direct initial contact upon membrane‐bridging SNARE interactions. Taken together, v‐SNAREs fulfill an essential role in exocytosis in which they are promiscuous and exhibit independently regulatory elements, which contribute to specificity of v‐SNARE action in wild‐type cells. Interestingly, the nearly complete loss of secretion, even with long‐lasting Ca2+ stimuli, clearly distinguishes double v‐SNARE deficiency from other SNARE knockout phenotypes (Yoshihara et al, 1999; Schoch et al, 2001; Sorensen et al, 2003), likely because it removes the majority of promiscuously acting SNAREs in the exocytotic pathway.
v‐SNARE specifics provide insight into the mode of SNARE function in exocytosis
Two distinct properties of granule exocytosis are affected by v‐SNARE proteins—the number of granules that readily undergo exocytosis and the mode of fusion pore expansion once exocytosis has been initiated. In neurons, sybII deficiency strongly reduces the response to hypertonic sucrose stimulation that measures the pool of readily releasable vesicles (Schoch et al, 2001). Both, the single‐knockout phenotypes and the rescue experiments in dko cells show that sybII supports a larger exocytotic burst than ceb. Since the sustained rate of secretion (reflecting ‘priming’) remains unchanged, the increased pool size in the presence of sybII is best explained by reduced ‘depriming’ of release‐ready granules. Importantly, the effects observed for the two cognate v‐SNAREs are remarkably similar to those found for different t‐SNARE variants of SNAP‐25, SNAP‐25A and SNAP‐25B (Sorensen et al, 2003). This suggests that the assembled (or assembling) SNARE complexes control the pool of release‐ready organelles and by this may provide the platform for auxiliary proteins to regulate exocytosis competence either by controlling the availability of SNAREs or their direct association. We find that structural components within the amino‐terminal domain (aa 1–37) of the v‐SNARE protein comprise key factors that regulate the priming stability of chromaffin granules. It remains to be shown whether the single amino‐acid difference (A37N) at the very N‐terminal end of the SNARE domain or the neighboring, nonconserved amino terminus (aa 1–32) is responsible for the differential regulation of the primed vesicle pool by the two v‐SNAREs. In any case, our results extend recent indications that SNAREs may partially assemble at their amino‐terminal ends in the exocytosis‐competent state, as judged from a differential sensitivity of neurotransmitter release to poisoning with TeNT and BoNT‐B (Hua and Charlton, 1999).
Previous studies led to opposing views on the mode of SNARE action in exocytosis, suggesting that these proteins are either dispensable before fusion (Tahara et al, 1998; Ungermann et al, 1998) or have an executive role (Weber et al, 1998; McNew et al, 2000). In the latter studies, using a lipid dequenching assay, SNAREs reconstituted in liposomes have been shown to be essential and sufficient for fusion on the time scale of minutes to hours, leaving the question unanswered whether SNARE action directly links lipid mixing to full membrane merger and fusion pore opening or simply generates a hemifused state from which liposomes may fuse in a SNARE‐independent fashion. We show that sybII and ceb differentially regulate the dynamics of the exocytotic fusion pore on a millisecond timescale. Thus, v‐SNARE function remains visible after initiation of exocytosis and is therefore intimately tied to the mechanism that makes vesicles fuse. Recent models hypothesize that SNARE proteins ‘zip’ from their membrane distant amino‐terminal ends toward the membrane proximal carboxy termini (for review, see Chen and Scheller, 2001). While differences in the amino‐terminal sequence of the v‐SNAREs alter the priming stability, their nonconserved carboxy‐terminal transmembrane domains (TMDs, amino‐acid identity 44%) may be responsible for the fusion pore effect. The TMDs of sybII and syntaxin directly interact via contiguous areas of interfacial residues (Margittai et al, 1999; Laage et al, 2000) that are only partially conserved within the TMD of ceb (Figure 6A). Since fusion of membranes likely involves the transition of a trans‐SNARE complex to its cis‐orientation (all proteins within the same membrane), alterations of SNARE assembly between their carboxy‐terminal TMDs can perturb local membrane curvature and fusion pore dilation.
In summary, the comparative analysis of different v‐SNAREs favors a model of sequential v‐SNARE action in rapid Ca2+‐triggered exocytosis, in which the amino terminus regulates v‐SNARE engagement and priming stability of the vesicles, the highly conserved SNARE motif ensures unperturbed initiation of exocytosis and the TMD controls the organelle's fusogenic properties.
Materials and methods
Mutant mice and cell culture
SybII and ceb mutant mice were maintained as heterozygotes by continuous crossbreeding with C57BL/6. ceb ko animals are viable and fertile. Thus, crossbreeding of the v‐SNARE‐deficient mouse strains allowed us to obtain animals that are heterozygous for sybII and homozygous knockouts for ceb. From the offspring of this generation, dko mutants were recovered at the expected Mendelian ratio (1.0:1.82:0.96; 109 animals, 19 preparations). These animals die at birth and exhibit a phenotype that compares well with the sybII ko phenotype (Schoch et al, 2001), having a tucked posture with neither spontaneous movements nor sensorimotor reflexes (Figure 2B). All analyses were performed on littermates at E17.5–18.5 derived from the heterozygote matings. Preparation and culturing of embryonic mouse chromaffin cells was performed as described (Sorensen et al, 2003). Recordings were performed at room temperature on days 1–3 of culture.
Whole‐cell capacitance measurements and caged Ca2+ photolysis
Recordings were performed with patch pipettes and an EPC‐9 amplifier (HEKA, Lambrecht, Germany). The Ringer's solution contained (in mM) 130 NaCl, 4 KCl, 2 CaCl2, 1 MgCl2, 10 HEPES, 48 glucose, pH 7.3 with NaOH. For measuring depolarization‐induced secretion, the pipette solution contained (in mM) 120 Cs‐glutamate, 8 NaCl, 0.18 CaCl2, 0.28 BAPTA, 1 MgCl2, 2 Mg‐ATP, 0.5 Na2GTP, 10 HEPES–CsOH, pH 7.3, 350 nM calculated free [Ca2+]i. Voltage‐dependent Ca2+ currents were isolated by blocking K+ and Na+ currents with TEA‐Cl (20 mM) and TTX (0.5 μM) added to the extracellular solution.
For ratiometric measurements of [Ca2+]i, a mixture of indicator dyes FURA‐2 and Furaptra (Molecular Probes, Eugene, OR) was excited at 340/380 nm with a monochromator (Polychrome IV, TILL Photonics, Planegg, Germany). Whole‐cell recordings with test solutions of defined calcium concentrations were used for in vivo calibration of the ratiometric Ca2+ signals. NP‐EGTA (supplied by G Ellis‐Davies, MCP Hahnemann University, Philadelphia, PA) was photolysed by a flash of ultraviolet light (xenon flash lamp, Rapp OptoElectronics, Hamburg, Germany) focused through a Zeiss objective (× 40, Fluar, 1.3) of an inverted microscope (Axiovert 200, Zeiss, Germany). The monochromator light was used to adjust [Ca2+]i after the flash by photolysing small amounts of NP‐EGTA. The pipette solution for flash experiments contained (in mM) 90 Cs‐aspartate, 10 NaCl, 4.63 CaCl2, 5 NP‐EGTA, 0.2 FURA‐2, 0.3 Furaptra, 2 Mg‐ATP, 0.3 Na2GTP, 40 HEPES, 17.5 d‐glucose, pH 7.3. For Ca2+ infusion of cells (10 μM free Ca2+), the pipette solution contained (in mM) 90 Cs‐aspartate, 10 NaCl, 10 DPTA, 6.8 CaCl2, 0.2 FURA‐2, 0.3 Furaptra, 2 Mg‐ATP, 0.3 Na2GTP, 40 HEPES, 17.5 d‐glucose, pH 7.3. Data were acquired with the Pulse software (HEKA, Lambrecht, Germany) and capacitance measurements were performed according to the Lindau–Neher technique (sine wave stimulus: 1000 Hz, 35 mV peak‐to‐peak amplitude, DC‐holding potential −70 mV). Current signals were digitized at 20 kHz and membrane capacitance was analyzed with customized IgorPro routines (Wavemetrics, Lake Oswego, OR). The flash‐evoked capacitance response was approximated with the following function: f(x)=A0+A1(1−exp(−(t)/τ1))+A2(1−exp(−(t)/τ2))+k(t), where A0 represents the cell capacitance before the flash. The parameters A1, τ1 and A2, τ2 represent the amplitudes and time constants of RRP and SRP, respectively.
Carbon fiber electrodes (Pan‐T650, 5 μm diameter, Amoco, Greenville, SC) were prepared as described (Bruns, 2004). Amperometric currents were recorded with EPC‐7 amplifier (HEKA, Lambrecht, Germany, electrode voltage +800 mV), filtered at 3 kHz (eight‐pole Bessel) and digitized gap‐free (25 kHz). For data collection and evaluation, the programs pClamp6 (Axon instruments, Foster City, CA) and AutesW (NPI Electronics, Tamm, Germany) were used. Signals were again digitally filtered at 3 kHz and analyzed with a customized event detection routine (Bruns et al, 2000). The analysis was restricted to events with a peak amplitude >4 pA and a total charge ranging from 10 to 1000 fC. The start of the ‘foot’ signal is defined as the time point where the current amplitude exceeds two times the standard deviation of the average baseline noise and it ends at the inflection point between the slowly increasing ‘foot’ signal and the more rapidly increasing spike current (Figure 7A). External solutions were delivered from a multichannel perfusion pipette (Bruns et al, 2000). Data were collected from release events stimulated by two applications of high K+‐containing Ringer's solution (in mM: 50 NaCl, 80 KCl, 2 CaCl2, 1 MgCl2, 48 glucose, 10 HEPES–NaOH, pH 7.3) given with an interval of 1 min. Stimulation periods were bracketed by superfusion of cells with Ringer's solution.
Chromaffin cells (plated on Thermanox coverslips, Nunc, Rochester, NY) were fixed with 3% glutaraldehyde and 2% paraformaldehyde in 0.1 M cacodylate buffer (pH 7.4), osmicated with 2% OsO4 in 0.1 M cacodylate buffer (pH 7.4) for 1 h at 4°C and serially dehydrated in ethanol followed by infiltration with Embed‐812 (EMS, München, Germany; polymerization 60°C, 48 h). Ultrathin sections (gray/silver interference color) were counterstained (2% uranyl acetate and lead citrate, 0.4 mg/ml, pH 12.0) and analyzed with a Philips Tecnai12 Biotwin electron microscope. The morphometric analyses were performed on randomly selected cells from three wild‐type, three ceb ko and four dko animals. Images acquired with a MegaView III CCD camera (Soft Imaging System, Münster, Germany) were analyzed with the Metamorph software (Universal Imaging, West Chester, PA). The number and spatial distribution of chromaffin granules were evaluated on micrographs (× 30 000 magnification, digitally zoomed to × 122 500) covering the entire cell's cytoplasmic region. The granule diameter was measured on micrographs (magnification × 49 000, digitally zoomed to × 205 000) as described (Bruns et al, 2000).
cDNAs encoding for sybII, ceb and TeNT light chain were subcloned into the viral plasmid pSFV1 (Invitrogen, San Diego, CA) upstream of an internal ribosome entry site that is followed by an open reading frame encoding for the enhanced green fluorescent protein (EGFP). EGFP labeling was used to identify infected cells. Preparation of virus particles was performed as described (Ashery et al, 1999).
Western blotting and immunocytochemistry
Whole mouse brain or adrenal gland extracts from embryos (E17.5–18) were prepared by homogenization in solution containing (in mM) 100 NaCl, 10 HEPES, 2 EDTA, 1 DTT, 2% Triton X‐100, pH 7.3. Homogenates were incubated on ice for 30 min and insoluble material was removed by centrifugation (Beckmann SS34; 13 000 r.p.m., 15 min, 4°C). Samples were separated by SDS–PAGE, analyzed by immunoblotting and immunoreactive bands were visualized with enhanced chemiluminescence. Mouse monoclonal antibodies against synaptobrevin II (69.1), syntaxin (HPC‐1), SNAP‐25 (71.2), synaptotagmin (41.1), synaptophysin, synaptotagmin 1 and NSF as well as rabbit sera raised against synaptobrevin I were kindly provided by R Jahn (Göttingen, Germany). The monoclonal antibody against TI‐VAMP and the rabbit serum against ceb were kindly provided by T Galli (Paris, France). ECL‐processed films were scanned and protein bands were densitometrically quantified using Metamorph software. Antibodies directed against sybII and ceb were affinity‐purified.
To determine changes in protein levels of sybII or ceb, chromaffin cells were processed for immunolabeling as described (Hannah et al, 1998). Epifluorescence pictures were acquired with an Imago‐CCD camera (TILL Photonics, Martinsried, Germany) and were analyzed using the Metamorph software. For quantification of the immunosignal, the average intensity of the fluorescent immunolabel was determined within an area of interest that comprises the outer cell perimeter.
Supplementary data are available at The EMBO Journal Online.
We express our gratitude to Drs E Neher and D Stevens for valuable discussions. We thank J Pessin (Stony Brook, NY) for providing the ceb ko animals and Drs G Nagy and J Sorensen for helping us to set up the mouse chromaffin cell culture. We are grateful to K Klingler, J Metzger, D Weber, M Wirth, K Wissel and C Bick for excellent technical assistance. The work was supported by grants from the DFG (SFB 530) and from the European Commission (QLG3‐CT‐2001‐02430) to DB and by HOMFOR.
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