Université de Paris, SPPIN-Saints Pères Paris Institute for the Neurosciences, CNRS, Paris, France.
Department of Cell Biology and Physiology, Washington University, St. Louis, United States.
Elife. 2020 Mar 31;9:e52137. doi: 10.7554/eLife.52137.
Central mammalian synapses release synaptic vesicles in dedicated structures called docking/release sites. It has been assumed that when voltage-dependent calcium entry is sufficiently large, synaptic output attains a maximum value of one synaptic vesicle per action potential and per site. Here we use deconvolution to count synaptic vesicle output at single sites (mean site number per synapse: 3.6). When increasing calcium entry with tetraethylammonium in 1.5 mM external calcium concentration, we find that synaptic output saturates at 0.22 vesicle per site, not at 1 vesicle per site. Fitting the results with current models of calcium-dependent exocytosis indicates that the 0.22 vesicle limit reflects the probability of docking sites to be occupied by synaptic vesicles at rest, as only docked vesicles can be released. With 3 mM external calcium, the maximum output per site increases to 0.47, indicating an increase in docking site occupancy as a function of external calcium concentration.
哺乳动物中枢突触在称为停靠/释放位点的专用结构中释放突触小泡。人们一直认为,当电压依赖性钙内流足够大时,突触输出达到每个动作电位和每个位点释放一个突触小泡的最大值。在这里,我们使用反卷积技术在单个位点上计算突触小泡输出(每个突触的平均位点数:3.6)。当在外钙浓度为 1.5 mM 的情况下用四乙铵增加钙内流时,我们发现突触输出在每个位点 0.22 个囊泡处达到饱和,而不是在每个位点 1 个囊泡处饱和。用钙依赖性胞吐作用的现有模型拟合结果表明,0.22 个囊泡的限制反映了在休息时停靠位点被突触小泡占据的概率,因为只有停靠的囊泡才能被释放。在外钙浓度为 3 mM 时,每个位点的最大输出增加到 0.47,表明作为外钙浓度函数的停靠位点占有率增加。