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The Journal of Neuroscience, November 15, 2000, 20(22):8377-8383

The Readily Releasable Pool of Vesicles in Chromaffin Cells Is Replenished in a Temperature-Dependent Manner and Transiently Overfills at 37°C

Vera Dinkelacker, Thomas Voets, Erwin Neher, and Tobias Moser

Department of Membrane Biophysics, Max-Planck-Institute for Biophysical Chemistry, D-37077 Göttingen, Germany

	ABSTRACT

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

Maturation of exocytic vesicles to the release-ready state is regulated by several factors, including intracellular calcium concentration ([Ca²⁺]_int) and the state of protein phosphorylation. Here we investigated the effects of temperature on the recovery from depletion of the readily releasable pool (RRP) of vesicles in adrenal chromaffin cells. Exocytosis and [Ca²⁺]_int were monitored by combined membrane capacitance and fura-2 measurements. At higher temperatures, a faster pool refilling and a larger RRP size were observed. The time constants of the recovery from depletion ranged from 3.6 to 1.1 sec (22 and 37°C, respectively) yielding a Q₁₀ of 2.3. The changes of the Ca²⁺ signal between the different temperatures could not account for the differences in recovery kinetics. At 32 and 37°C, we observed a transient overfilling of the RRP after pool depletion, which stands in clear contrast to the sustained secretory depression seen at lower temperatures. The overshoot in RRP size was very prominent in cells with lower basal [Ca²⁺]_int, hence with a large difference between prestimulus and poststimulus [Ca²⁺]_int. In cells with higher basal [Ca²⁺]_int, the pool was larger under steady-state conditions but showed less overfilling on stimulation. We conclude that vesicle maturation is markedly accelerated at physiological temperature, thus allowing for a rapid adaptation of the pool size to the relatively short-lived Ca²⁺ transient.

Key words: exocytosis; chromaffin cells; capacitance; vesicle pools; refilling; temperature; calcium

	INTRODUCTION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

The regulation of a readily releasable pool (RRP) of vesicles has for a long time been discussed as a major mechanism of exocytic plasticity in both neuroendocrine cells and presynaptic terminals (for review, see Zucker, 1999). In this context, the depression of the secretory response and ensuing recovery is interpreted as refilling of a depleted RRP. Previous studies of this recovery process were performed in various preparations (Stevens and Tsujimoto, 1995; Moser and Neher, 1997b; von Gersdorff and Matthews, 1997; Wang and Kaczmarek, 1998; Moser and Beutner, 2000) and revealed regulation by Ca²⁺ and protein kinases (Smith et al., 1998; Stevens and Sullivan, 1998; Gomis et al., 1999). Adrenal chromaffin cells are embryonically derived from precursors of sympathetic neurons and release catecholamines into the bloodstream using the same conserved fusion machinery that is found in the CNS (Morgan and Burgoyne, 1997). These cells offer the advantage of allowing simultaneous monitoring of cytosolic Ca²⁺ and high time resolution measurements of secretion. For these reasons, they have been extensively studied as a model system for neurosecretion.

Several studies indicated that temperature has substantial influence on exocytosis. Chromaffin cells under continuous stimulation displayed increased initial amounts and rates of secretion at 37°C compared with room temperature (Kao and Westhead, 1984; Park et al., 1999). Thomas et al. (1993b) investigated the influence of temperature on secretion evoked by flash photolysis of Ca²⁺ using high resolution membrane capacitance measurements in pituitary melanotrophs. They reported a strong enhancement of a slow secretory component most likely reflecting increased supply of release-ready vesicles. This conclusion was also drawn from a study of temperature effects on insulin release from pancreatic B-cells induced by trains of depolarizations (Renstrom et al., 1996).

The objective of the present study was to monitor the replenishment of release-ready vesicles in a more direct and highly time-resolved manner, considering both the temperature and the Ca²⁺ dependence of the process. To mimic in vivo conditions, membrane capacitance measurements (C_m) were performed in the perforated-patch configuration, which preserves mobile cytosolic components. [Ca²⁺] was recorded simultaneously using fura-2 AM. We examined the recovery time course of the RRP from depolarization-induced depletion in isolated bovine adrenal chromaffin cells at 22, 27, and 32°C and at physiological temperature (37°C). Our intention was to distinguish the genuine temperature effects on vesicle dynamics from the indirect effects mediated by changes in Ca²⁺ signaling. Previous work has shown that the RRP refilling is enhanced at increased intracellular [Ca²⁺]. Here we show that the process is highly temperature dependent, such that above 32°C, the pool size rapidly adapts to the short-lived rise in [Ca²⁺]_int.

	MATERIALS AND METHODS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

Chromaffin cell culture. Chromaffin cells were prepared by digestion of adult bovine adrenal medulla in collagenase type I (0.5 mg/ml; Worthington Enzymes, Freehold, NJ) and cultured for 1-4 d. Additional details are described in Smith (1999). After enrichment on a Percoll gradient, cells were plated in DMEM, 1 × GMS-X (a defined serum substitute; Life Technologies, Bethesda, MD), penicillin, and streptomycin at a density of ~4.4 × 10³/mm². Cultures were maintained at 37°C and 10% CO₂.

Solutions. During recordings, cells were constantly superperfused at a rate of ~1 ml/min with a Ringer's solution of the following composition (in mM): 150 NaCl, 10 HEPES, 10 glucose, 2.8 KCl, 2 MgCl_2, 2 CaCl₂ (recovery at 32 and 37°C), or 10 CaCl₂ (all other conditions). The osmolarity was adjusted to 310 mOsm with mannitol, and pH was adjusted to 7.2 with NaOH. The standard perforated patch solution contained (in mM): 145 Cs-glutamate, 10 HEPES, 8 NaCl, 1 MgCl_2, 0.53 amphotericin B; pH was adjusted to 7.2 with CsOH, and osmolarity was 300 mOsm. Amphotericin B was prepared as described by Smith and Neher (1997). Pipettes were tip-dipped in amphotericin-free solution for 2-10 sec and back-filled with freshly mixed amphotericin-containing solution. The liquid junction potential between the extracellular Ringer's and the pipette filling solution was measured to be ~13 mV, and all potentials were adjusted accordingly. All chemicals were obtained from Sigma (St. Louis, MO), with the exception of CsOH (Aldrich, Milwaukee, WI) and amphotericin B (Calbiochem, La Jolla, CA), or as noted otherwise.

Electrophysiological measurements. Pipettes of ~2-3 M resistance were pulled from borosilicate glass, partially coated with a silicone compound (G. E. Silicones, Bergen Op Zoom, The Netherlands), and lightly fire-polished. For acquisition we used an EPC-9 amplifier and "PULSE" software running on an Apple Macintosh. C_m was estimated by the Lindau-Neher technique (for review, see Gillis, 1995) implemented as the "Sine + D.C." feature of the Pulse lock-in module. An 800 Hz, 35 mV peak amplitude sinewave was applied to a holding potential of 83 mV, and the reversal potential of the lock-in module was set to 0 mV. Data were acquired through a combination of the high time resolution PULSE software and the lower time resolution X-Chart plug-in module to the PULSE software. Briefly, membrane current was sampled at 10 kHz shortly (100 msec) before, during, and after the depolarizations, and C_m was calculated with a resolution of 800 Hz. Data acquired between high time resolution PULSE protocols were typically sampled at 12 Hz with the lower time resolution X-Chart plug-in.

Capacitance increases caused by depolarizations were determined from the high time resolution C_m traces as the difference between mean C_m measured in a 13 msec window starting 38 msec after the depolarization minus the mean prestimulus C_m, also measured over a 13 msec window. The first 38 msec of the post-depolarization capacitance was neglected to avoid influences of nonsecretory capacitance transients (Horrigan and Bookman, 1994).

Temperature control. Temperatures were adjusted by flow-heating and heating of the objective lens (TC-344B, Warner, Hamden, CT) as well as heating the microscope stage (Luigs and Neumann, Ratingen, Germany). Without heating the objective lens, a pronounced temperature difference of up to 3°C was observed between the edge and the center of the coverslip. Temperature was measured close to the recorded cell. Experiments were performed at either 22, 27, 32, or 37°C.

Cytosolic Ca²⁺ measurements. After the cells were preincubated in growth medium containing 1 µM fura-2 AM (Molecular Probes, Eugene, OR) for 20 min at 37°C, cellular Ca²⁺ concentrations were measured in the perforated-patch configuration by excitation of the dye with light alternated between 360 and 390 nm using a monochromator-based system (TILL Photonics, Planegg, Germany). Once the experimental protocol was finished, the perforated patch was ruptured, causing the intracellular fura-2 to dialyze out of the cell, allowing for the measurement of the autofluorescence of the cell. The autofluorescence values at 360 and 390 nm wavelength excitation were subtracted from values measured during the experiment, and the [Ca²⁺]_int was estimated according to Grynkiewicz and colleagues (1985).

	RESULTS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

The secretory response to dual-pulses at different temperatures

Chromaffin cells were stimulated by pairs of depolarizations (Fig. 1). This stimulus, termed a dual-pulse (Gillis et al., 1996), is designed to elicit secretory depression by means of two identical Ca²⁺ current injections given in rapid succession. A value <1 for the ratio (R) of the two capacitance responses (R = C_m2/C_m1) represents secretory depression, presumably because of the depletion of the RRP. The sum (S = C_m1 + C_m2) is a suitable estimate of the size of the RRP of vesicles (Fig. 1A) if depletion is observed. In the temperature range investigated, substantial pool depletion occurred as shown in Figure 1, A and B, as well as Table 1. Nevertheless, Ca²⁺ currents were not always large enough to elicit sufficient depression. Therefore, we limited the analysis to the pairs of dual-pulses with R < 0.7 for the first depleting dual-pulse. This excluded ~40% of the dual-pulses from the data set acquired at 22°C and a comparable percentage at higher temperatures (Table 1).

View larger version (14K): [in this window] [in a new window]   Figure 1.   The secretory response at different temperatures. A, Example of the Ca2+ currents (bottom trace) and capacitance responses (Cm, top trace) to a dual-pulse of a cell held in the perforated patch mode at room temperature (22°C). Two step depolarizations of 100 msec with a 100 msec interval were applied. The depolarization potentials were adjusted such that the two Ca2+ current injections matched closely. Summed response S = 40 fF; ratio R = 0.18. B, Ca2+ currents and capacitance responses of a cell at 37°C. S = 206 fF; R = 0.23. Note the strong increase in capacitance response compared with 22°C and the pronounced Na+ current gating artifact (Horrigan and Bookman, 1994). A slightly diminished Ca2+ current amplitude of the second pulse was tolerated because residual [Ca2+]int is expected to enhance the stimulus strength. C, Exocytosis-Ca2+ relationship. The first capacitance response of a dual-pulse (Cm1) under steady-state conditions was plotted versus the Ca2+ current integral of the corresponding depolarization. Filled black triangles are data at 22°C, filled red squares at 27°C, green circles at 32°C, and filled blue diamonds at 37°C. Exocytic responses to a given Ca2+ stimulus became larger with the rise in temperature.

View this table: [in this window] [in a new window]   Table 1.   Summary of the recovery data (values are given as mean ± SEM)

In Figure 1A, a typical response of a cell at room temperature (22°C) is shown. Experimental parameters were chosen to maximize the stimulus-induced depression; e.g., we used 10 mM [Ca²⁺]_ext to provide for large Ca²⁺ current amplitudes and used long durations of depolarizations (100 msec). At 32 and 37°C, a high percentage of dual-pulses evoked rapid endocytosis (data not shown). In these cases, the C_m measurements, which track net changes in cell surface, do not allow for determination of the exact amount of exocytosis. By lowering [Ca²⁺]_ext from 10 to 2 mM, we were able to drastically reduce the incidence of rapid endocytosis (Fig. 1B, 37°C, 2 mM [Ca²⁺]_ext). This is in line with the previously observed [Ca²⁺] dependence of rapid endocytosis (Artalejo et al., 1995; Smith and Neher, 1997; Engisch and Nowycky, 1998; Mansvelder and Kits, 1998). The use of 10 mM [Ca²⁺]_ext at 22 and 27°C and 2 mM at 32 and 37°C allowed for reliable measurements of the exocytic response. These conditions were used for all of the data presented below.

At 37°C, the secretory response was markedly enhanced as compared with room temperature, despite apparently smaller Ca²⁺ currents (Fig. 1B). The Ca²⁺-exocytosis relationship at the different temperatures was further investigated as shown in Figure 1C. The large range of the Ca²⁺ currents in this analysis most likely originates from rundown during an experiment, possibly also from differences in the size of the chromaffin cells and the set of Ca²⁺ channels. Despite considerable scatter, there is a discernible trend of higher secretion amplitudes for a given Ca²⁺-current magnitude with the rise in temperature. Between 45 and 50 pC, a range that approximates the overall average Ca²⁺ current integral to a 100 msec depolarization, the mean capacitance responses were 36 ± 4 fF at 22°C, 60 ± 2 fF at 27°C, 132 ± 10 fF at 32°C, and 162 ± 15 fF at 37°C.

Recovery from pool depletion at room temperature

To monitor the recovery of the RRP from depletion, we estimated the size of the RRP at resting conditions with an initial dual-pulse. This stimulus had to be strong enough to deplete the pool of release-ready vesicles. A second dual-pulse was applied at varying time intervals to probe the recovery from depletion.

Figure 2A displays the recovery time course, i.e., the RRP size estimates (S) of a representative cell at 22°C as a function of the interpulse interval. The pooled data of the nine cells measured at room temperature and their average changes in cytosolic [Ca²⁺]_int are shown in Figure 2B. Note also the basal Ca²⁺ concentration at 22°C and elevated temperatures as given in Figure 3E.

View larger version (14K): [in this window] [in a new window]   Figure 2.   Analysis of capacitance responses to paired depolarizations. A, Summed capacitance responses of a representative cell at 22°C plotted versus the interpulse interval. The shortest time interval between dual-pulses was 2 sec at 22°C and 0.5 sec for all other temperatures. B, Averaged capacitance responses () and fura-2 AM measured [Ca2+]int () of nine cells. The steady-state pool size is 62 ± 2 fF as determined by an average of the points at 30 sec and longer time intervals. The peak [Ca2+]int was measured within the first 20 msec after the second depolarization.

View larger version (32K): [in this window] [in a new window]   Figure 3.   Properties of the Ca2+ signal at different temperatures. A, Summed Ca2+ current integrals of dual-pulses at different temperatures, including the value at 37°C and 10 mM [Ca2+]ext (n = 7). B, Peak Ca2+ currents at 22 and 37°C (left) as determined from the first of the dual-pulses, 5 msec average at 5 msec after the onset of the current, i.e., after Na+ current inactivation. The final Ca2+ currents (right, 5 msec average at 95-100 msec) attain 70 and 55% of the peak currents at 22 and 37°C, respectively. C, Peak cytosolic [Ca2+] from fura-2 AM measurements (average of the mean of all cells). D, Decay time constants of [Ca2+]int derived from exponential fits of the first five dual-pulses of five cells at each temperature (data not shown); the peak [Ca2+] and the ensuing 3 sec were not included in the fit. E, Basal cytosolic [Ca2+] from fura-2 AM measurements (steady-state values after the first 5 stimulations were averaged over 2 sec).

The recovery of pool size shows a rapid onset while the decaying [Ca²⁺]_int is still high, because of a strong Ca²⁺ enhancement of the vesicle supply [Smith et al. (1998); data acquired at room temperature], whereas steady-state values are slowly approached after [Ca²⁺]_int has decayed to basal values. The steady-state pool size as determined between 30 and 65 sec after the depleting stimulus was 62 ± 2 fF (also see Table 1). Assuming a mean capacitance of ~2 fF per dense-core vesicle in adrenal chromaffin cells (estimates range from 1.3 to 2.7 fF) (Neher and Marty, 1982; Chow et al., 1996; Albillos et al., 1997; Moser and Neher, 1997a), this pool size corresponds to ~30 vesicles.

Ca²⁺ kinetics at different temperatures

To compare the kinetics of the vesicle supply at different temperatures, we had to address the following issue. Pool-depleting depolarizations lead to a rise in [Ca²⁺]_int within the time window of vesicle replenishment. Accordingly, the genuine temperature dependence of the recovery process can only be approximated if the properties of the Ca²⁺ signal remain similar throughout the temperature range investigated. We therefore analyzed the Ca²⁺ currents as well as the resulting changes of cytosolic [Ca²⁺] monitored by fura-2 measurements (Fig. 3A-E).

The summed Ca²⁺ current integral of the paired Ca²⁺ current injections, a measure of the stimulus strength, is shown in Figure 3A. The current integrals were comparable for 22 and 37°C at 10 mM [Ca²⁺]_ext, whereas they were smaller at 37°C and 2 mM [Ca²⁺]_ext (Fig. 3A). Note that we used 10 mM [Ca²⁺]_ext at 22 and 27°C and 2 mM [Ca²⁺]_ext at 32 and 37°C in all of the experiments presented above and for the following set of analysis.

The origins of the smaller Ca²⁺ current integrals at higher temperatures, most obvious at 37°C, are twofold. On one hand, the reduction in external [Ca²⁺] leads to slightly smaller peak Ca²⁺ currents (Fig. 3B). On the other, the Ca²⁺ currents inactivate much faster at 37°C as compared with room temperature (Fig. 3B; see also Fig. 1A,B). Such speeding of the inactivation of Ca²⁺ currents at higher temperatures has also been reported for melanotropic cells (Mansvelder and Kits, 1998). Given the equivalent or smaller Ca²⁺ current integrals as compared with 22°C, the increased amount of secretion at higher temperatures is not the result of a stronger stimulus. Rather, an enhanced effectiveness of Ca²⁺-eliciting exocytosis must be postulated.

Decreased peak values for [Ca²⁺]_int were found at higher temperatures (Fig. 3C), mostly because of the lower [Ca²⁺]_ext at 32 and 37°C. Although faster than at 22°C, the decay time constants did not differ significantly between 27, 32, and 37°C (Fig. 3D). Thus, the observed acceleration of the recovery process at higher temperatures relative to 27°C (see below) cannot be explained by any concomitant change in the kinetics or amplitudes of poststimulus [Ca²⁺].

RRP recovery at elevated temperatures

The time courses of the recovery from pool depletion at different temperatures are shown in Figure 4. The absolute values were corrected for rundown during an experiment by normalizing the S-value of a dual-pulse to the one of the preceding depleting dual-pulse. This preceding stimulus had been applied at resting [Ca²⁺]_int, with a time interval of ~50 sec to its predecessor.

View larger version (12K): [in this window] [in a new window]   Figure 4.   Normalized RRP size at different temperatures. Sum capacitance responses were normalized to the previous dual-pulse, averaged, and plotted versus the interpulse interval. Data points up to 10 sec were fit by a monoexponential. A, 22°C (9 cells), t = 3.6 sec; B, 27°C (5 cells), t = 3.2 sec; C, 32°C (7 cells), t = 1.7 sec. Data points marked with an asterisk are significantly different from the steady-state value (p < 0.02). D, 37°C (8 cells), t = 1.1 sec; data marked by an asterisk are significantly different from steady-state value (p < 0.05). E, Arrhenius plot of the rate constants: rate constants were derived from monoexponential fits in A-D. Their logarithms were plotted versus 1000/T (absolute temperature); the top axis shows the corresponding temperatures in degrees centigrade. The slope of the line fit yields an energy of activation of 63 kJ/mol. The Q10 as calculated from the Arrhenius equation is 2.3 at 22°C.

Assuming that each stimulus releases the same fraction of the pool, the intercept S_int at time 0 is derived according to S_int = S₀ × R², with S₀ = 1 for the normalized data (Gillis et al., 1996). The average ratios R for the different temperatures are given in Table 1. R was 0.45 ± 0.01 at room temperature, including only those dual-pulses that follow the depletion criteria. This yields S_int = 0.20 as an estimate of the relative initial pool size immediately after the dual-pulse.

The decay time constants (_dec) of the cytosolic [Ca²⁺] were shown to be 3-4 sec for the temperatures investigated (Fig. 3D). A time window of 3 × _dec (10 sec) was chosen for analysis of RRP refilling, in which [Ca²⁺] was assumed to be comparably elevated at the different temperatures. For the normalized recovery data acquired at room temperature, exponential fitting in this time window yielded a time constant of 3.6 sec (Fig. 4A).

Raising the temperature led to both an increase in the secretory response and an acceleration of the recovery from pool depletion (Fig. 4 A-D). These effects were moderate at 27°C (Fig. 4B) but very pronounced when reaching higher temperatures. The steady-state RRP size at basal [Ca²⁺] as well as the time constants of the RRP recovery at the different temperatures are summarized in Table 1.

At 32°C, the time constant of recovery was 1.7 sec. The steady-state pool size was more than doubled [151 ± 10 fF corresponding to 75 vesicles (Table 1)]. From the fit at 37°C, a time constant of 1.1 sec is derived. This value has to be taken with some caution because the pool size of the initial depleting stimulus is already restored within <1 sec (Fig. 4D). The fast time course indicates that some vesicle recruitment may already have occurred during the stimulation episode (300 msec), thus limiting the accuracy of our stimulation protocol.

The temperature dependence of the rate constants of recovery (k, the reciprocal of the time constant) was reasonably well fitted by the Arrhenius equation (Fig. 4E):
where E_A represents the energy of activation of the process, R represents the molar gas constant, and A represents an empirical factor (Arrhenius, 1901; Atkins, 1986). This type of relationship suggests that the same reaction step remains rate-limiting over the temperature range investigated. From the E_A value of 63 kJ/mol, the Q₁₀ was calculated according to Q₁₀ = k(T + 10K)/k(T), yielding a value of 2.3 at 22°C.

The Q₁₀ values of chemical reactions generally lie between 2 and 4, whereas those of physical processes such as diffusion range between 1.1 and 1.4 (Precht et al., 1973). Hence, our findings rather point toward a temperature-sensitive protein reaction than to a mere acceleration of vesicle transport attributable to diffusional processes.

The RRP transiently overfills at 32 and 37°C

At elevated temperatures, we observed a marked change in the recovery behavior. At both 32 and 37°C, the RRP size exceeded the level of the previous pulse for a brief period after stimulation and relaxed toward the lower steady-state pool size within ~20 sec (Fig. 4C,D). This prominent overshoot of the RRP size is likely to be a consequence of the marked acceleration of vesicle recruitment at elevated [Ca²⁺]_int (Smith et al., 1998). If elevated temperature further increases the recruitment rate, it is possible that the RRP overfills before [Ca²⁺]_int decays back to baseline; then the overshoot should be more prominent, the larger the difference in prestimulus and poststimulus [Ca²⁺]_int.

To examine this possibility, we divided the cells at 37°C into groups with lower and higher basal [Ca²⁺] (Fig. 5). Four cells with [Ca²⁺]_int <250 nM (mean 189 ± 6 nM) had an average RRP size of 85 ± 10 fF (Fig. 5B). Under the conditions of low basal [Ca²⁺]_int, a very pronounced poststimulus augmentation was observed (Fig. 5A). As soon as 500 msec after the first dual-pulse, the secretory response exceeded the previous response, reaching a maximum of ~1.75 times the steady-state pool size after 2 sec. Approximately 10 sec after the stimulus, when [Ca²⁺] had returned to basal values (Fig. 5B), the C_m response started to decay from the overfilled to the steady-state level. This time course is consistent with the postulated Ca²⁺ enhancement of the vesicle supply.

View larger version (32K): [in this window] [in a new window]   Figure 5.   Refill kinetics at low and high basal [Ca2+]. A, Cells with low basal [Ca2+] (mean 189 ± 14 nM, ) display a very prominent overshoot of the pool size shortly after the stimulus. The values marked with asterisks (at 1, 2, and 5 sec) are significantly different (p < 0.05) from both the steady-state values and the respective values at higher basal [Ca2+] (mean 348 ± 25 nM, n = 4, ). Both populations displayed similar depletion levels as indicated by Sint. The inset shows the rundown-corrected capacitance responses in absolute values. Note that the responses attained within the first 2 sec after depletion were comparable in both data sets. At high basal [Ca2+], however, the pool size continued to rise to the much larger steady-state size. B, RRP size and properties of the Ca2+ signal for cells with low and high basal [Ca2+] (189 nM, black bars; 348 nM, white bars).

Four other cells had a basal [Ca²⁺] between 250 and 400 nM (mean 348 ± 11 nM). Their steady-state RRP size was twice that of the cells at lower basal [Ca²⁺] (170 ± 23 fF) (Fig. 5B), which again is in line with the expected Ca²⁺ effect on the vesicle supply. In this data set, the capacitance response attained within the first 2 sec after depletion was comparable with the one in the cells at lower basal [Ca²⁺] (Fig. 5A, inset). However, the pool size continued to rise to the much larger steady-state size, showing hardly any overshoot during the recovery from depletion.

These findings suggest that the overfilling of the RRP is reflective of the accelerated vesicle transitions at elevated temperatures, which allow for a dynamic adaptation of the RRP to the short-lived rise in [Ca²⁺]_int.

	DISCUSSION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

In this study, we have provided evidence that the maturation of vesicles to the release ready state is markedly enhanced at physiological temperature. As a result, restoration of full exocytic competence is faster and secretory efficiency is higher when compared with room temperature, the condition under which secretion experiments are usually performed. The accelerated vesicle replenishment at elevated temperatures did not originate from a stronger stimulus because the Ca²⁺ signals were comparable to or smaller than those at room temperature.

Our conclusion of a strong temperature dependence of the vesicle supply is in line with the biochemical data of Bittner and Holz (1992), who showed a highly temperature-sensitive step in the secretory process after an ATP-dependent step and preceding the final Ca²⁺-dependent fusion of vesicles. Previous electrophysiological data also support an enhanced recruitment of vesicles at higher temperatures (Thomas et al., 1993b; Renstrom et al., 1996).

In addition, our study provides a quantitative and highly time-resolved description of the RRP recovery from depletion at different temperatures.

Beyond the anticipated acceleration by temperature, the data reveal a transient overfilling of the RRP at 32 and 37°C. This overfilling reflects the Ca²⁺ dependence of the vesicle supply because it is more prominent the larger the difference in prestimulus and poststimulus [Ca²⁺]_int. The RRP size exceeds the steady-state value during the short-lasting elevation of [Ca²⁺]_int and relaxes back toward it once [Ca²⁺]_int has declined to baseline. This dynamic adaptation of the secretory response to the rise in [Ca²⁺]_int stands in clear contrast to the pronounced depression at 22°C, which lasts several seconds. At 32 and 37°C, the time window of depression is hardly perceived. Rather, the quick onset of augmentation is the most prominent feature. This discrepancy sheds some doubt on the simple extrapolation from data acquired at room temperature to the findings at physiological temperature.

The accelerated vesicle replenishment and ensuing transient overfilling at elevated temperatures are indicative of a faster equilibration between the RRP and proximal vesicle pools. When this overshoot was simulated with the two-step model of secretion control (Heinemann et al., 1993; Smith et al., 1998), the relaxation toward the steady-state pool size at basal [Ca²⁺]_int could only be accounted for if both forward and backward rate of exchange between RRP and reserve pool were increased by temperature.

Recently, a refined model of secretion has been proposed (Voets et al., 1999) that is based on the comparison between the vesicle populations released in response to voltage-dependent Ca²⁺ influx and flash-photolysis of caged Ca²⁺. Flash-photolysis elicits a biphasic exocytic burst. In the model, the RRP recruited by depolarizations corresponds to the vesicle population released during the fast component of the burst. The slow component, termed the slowly releasable pool (SRP), remains after RRP depletion. It constitutes an intermediate to the formerly described reserve pool of vesicles. The SRP can only be directly fused during prolonged episodes of high [Ca²⁺]_int and may be involved in the rapid resupply of vesicles to the RRP.

Because our study was focused on depolarization-induced secretion, the observed temperature effects reflect changes of the RRP rather than of the SRP. In a flash photolysis study on melanotrophs, Thomas et al. (1993a,b) did not observe a significant increase of the exocytic burst amplitude when increasing the temperature from 24 to 34°C. Our study, however, reveals an increase of pool size by a factor of 2 when the temperature is raised by 10°C. These findings could be reconciled if the vesicle transitions that we observed originated from a shift between the SRP and the RRP and the flash experiments of Thomas and colleagues (1993a,b) determined the sum of the SRP and the RRP.

How do the data obtained in neuroendocrine cells relate to neurons? The results of Hardingham and Larkman (1998), who found that synaptic connections became successively more reliable with the elevation of temperature, can well be explained with an increased number of readily releasable vesicles at higher temperatures, as described here for neuroendocrine cells. As to the refilling of the RRP, the time constants reported in neuronal preparations range from 3 to 10 sec at room temperature (von Gersdorff and Matthews, 1997; Stevens and Sullivan, 1998; Stevens and Wesseling, 1998; Weis et al., 1999) and at 36°C (Stevens and Tsujimoto, 1995). Interestingly, a recent direct comparison of the recovery process at 25 and 35°C in hippocampal neurons (S. Pyott and C. Rosenmund, unpublished observations) revealed an acceleration by a factor of 3 with the rise in temperature, comparable with our present findings. Despite differences in signal-secretion coupling between synapses and neuroendocrine cells (Chow et al., 1992), this evidence points toward a similar regulation of the size of the RRP.

If not limited by endocytosis, it will be interesting to test whether the temperature-sensitive steps in vesicle maturation can be further resolved by combined flash-photolysis and depolarization experiments. This would also allow for comparison with the quantitative predictions of the model of Voets et al. (1999).

	FOOTNOTES

Received May 22, 2000; revised Aug. 21, 2000; accepted Aug. 24, 2000.

This work was supported by grants of the Deutsche Forschungsgemeinschaft (SFB 523). We thank Dr. Corey Smith for providing analysis routines and for helpful discussions. We thank Drs. Kevin Gillis, Christophe Pouzat, and Ralf Schneggenburger for critical comments on former versions of this manuscript, and we thank F. Friedlein and M. Pilot for expert technical assistance.

Correspondence should be addressed to Vera Dinkelacker, Department of Membrane Biophysics, Max-Planck-Institute for Biophysical Chemistry, Am Fassberg, D-37077 Göttingen, Germany. E-mail: vdinkel{at}gwdg.de.

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Copyright © 2000 Society for Neuroscience  0270-6474/00/20228377-07$05.00/0

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