Graduate School of Brain Science, Doshisha University, Kyotanabe, Kyoto, Japan.
J Physiol. 2019 Aug;597(16):4373-4386. doi: 10.1113/JP278040. Epub 2019 Jul 25.
We used presynaptic capacitance measurements at the hippocampal mossy fibre terminal at room temperature to measure Ca-dependence of exo- and endocytotic kinetics. The readily releasable pool (RRP) of synaptic vesicles was released with a time constant of 30-40 ms and was sensitive to Ca buffers, BAPTA and EGTA. Our data suggest that recruitment of the vesicles to the RRP was Ca-insensitive and had a time constant of 1 s. In addition to the RRP, the reserve pool of vesicles, which had a similar size to RRP, was depleted during repetitive stimulation. Our data suggest that synaptic vesicle endocytosis was also Ca-insensitive.
Hippocampal mossy fibre terminals comprise one of the cortical terminals, which are sufficiently large to be accessible by patch clamp recordings. To measure Ca-dependence of exo- and endocytotic kinetics quantitatively, we applied presynaptic capacitance measurements to the mossy fibre terminal at room temperature. The time course of synaptic vesicle fusion was slow, with a time constant of tens of milliseconds, and was sensitive to Ca buffers EGTA and BAPTA, suggesting a loose coupling between Ca channels and synaptic vesicles. The size of the readily-releasable pool (RRP) of synaptic vesicles was relatively insensitive to Ca buffers. Once the RRP was depleted, it was recovered by a single exponential with a time constant of ∼1 s independent of the presence of Ca buffers, suggesting Ca independent vesicle replenishment. In addition to the RRP, the reserve pool of vesicles was released slowly during repetitive stimulation. Endocytosis was also insensitive to Ca buffers and had a slow time course, excluding the involvement of rapid vesicle cycling in vesicle replenishment. Although mossy fibre terminals are known to have various forms of Ca-dependent plasticity, some features of vesicle dynamics are robust and Ca-insensitive.
我们在室温下使用海马苔藓纤维末梢的突触前电容测量来测量外排和内吞动力学的钙依赖性。突触小泡的易释放池(RRP)以 30-40ms 的时间常数释放,并对 Ca 缓冲剂 BAPTA 和 EGTA 敏感。我们的数据表明,囊泡向 RRP 的募集是钙不敏感的,时间常数为 1s。除了 RRP 之外,储备池的囊泡在重复刺激期间也被耗尽,其大小与 RRP 相似。我们的数据表明,突触囊泡内吞作用也是钙不敏感的。
海马苔藓纤维末梢是皮层末梢之一,其大小足以通过膜片钳记录进行测量。为了定量测量外排和内吞动力学的钙依赖性,我们在室温下对苔藓纤维末梢进行了突触前电容测量。突触小泡融合的时程较慢,时间常数为数十毫秒,对 Ca 缓冲剂 EGTA 和 BAPTA 敏感,表明 Ca 通道和突触小泡之间的偶联松散。突触小泡易释放池(RRP)的大小对 Ca 缓冲剂相对不敏感。一旦 RRP 耗尽,它就会通过一个时间常数约为 1s 的单指数恢复,而与 Ca 缓冲剂的存在无关,这表明囊泡补充是钙独立的。除了 RRP 之外,储备池的囊泡在重复刺激期间也会缓慢释放。内吞作用也对 Ca 缓冲剂不敏感,时程较慢,排除了快速囊泡循环在囊泡补充中的参与。尽管苔藓纤维末梢已知具有各种形式的 Ca 依赖性可塑性,但囊泡动力学的某些特征是稳健的且钙不敏感的。