Coco S, Verderio C, De Camilli P, Matteoli M
CNR Cellular and Molecular Pharmacology Center, Department of Medical Pharmacology, Milano, Italy.
J Neurochem. 1998 Nov;71(5):1987-92. doi: 10.1046/j.1471-4159.1998.71051987.x.
Using an immunocytochemical assay to monitor synaptic vesicle exocytosis/endocytosis independently of neurotransmitter release, we have investigated some aspects of vesicle recycling in hippocampal neurons at different developmental stages. A calcium- and depolarization-dependent exocytotic/endocytotic recycling of synaptic vesicles was found to take place in neurons already before the formation of synaptic contacts. The analysis of synaptic vesicle recycling at different calcium concentrations revealed the presence of two release components: the first one activated by low calcium concentrations and sustaining vesicle recycling before synaptogenesis, and a second one activated by high calcium concentrations, which is specifically turned on after the establishment of synaptic contacts. These data suggest that formation of synapses correlates with the activation of a putative low-affinity calcium sensor, which allows synaptic vesicle exocytosis to be triggered and turned off over extremely short time scales, in response to large increases in the level of intracellular calcium.
我们使用免疫细胞化学分析方法独立于神经递质释放来监测突触小泡的胞吐作用/内吞作用,研究了不同发育阶段海马神经元中突触小泡循环利用的某些方面。发现在突触接触形成之前,神经元中就已经发生了依赖于钙和去极化的突触小泡胞吐/内吞循环利用。对不同钙浓度下突触小泡循环利用的分析揭示了存在两种释放成分:第一种由低钙浓度激活,在突触发生之前维持突触小泡循环利用;第二种由高钙浓度激活,在突触接触建立后特异性开启。这些数据表明,突触的形成与一种假定的低亲和力钙传感器的激活相关,该传感器能够响应细胞内钙水平的大幅升高,在极短的时间尺度内触发并关闭突触小泡的胞吐作用。