Midorikawa Mitsuharu, Okamoto Yuji, Sakaba Takeshi
Graduate School of Brain Science, Doshisha University, Kyoto, 6190225, Japan
Graduate School of Brain Science, Doshisha University, Kyoto, 6190225, Japan.
J Physiol. 2014 Aug 15;592(16):3495-510. doi: 10.1113/jphysiol.2014.273243. Epub 2014 Jun 6.
At the mammalian central synapse, Ca(2+) influx through Ca(2+) channels triggers neurotransmitter release by exocytosis of synaptic vesicles, which fuse with the presynaptic membrane and are subsequently retrieved by endocytosis. At the calyx of Held terminal, P/Q-type Ca(2+) channels mainly mediate exocytosis, while N- and R-type channels have a minor role in young terminals (postnatal days 8-11). The role of each Ca(2+) channel subtype in endocytosis remains to be elucidated; therefore, we examined the role of each type of Ca(2+) channel in endocytosis, by using whole-cell patch-clamp recordings in conjunction with capacitance measurement techniques. We found that at the young calyx terminal, when R-type Ca(2+) channels were blocked, the slow mode of endocytosis was further slowed, while blocking of either P/Q- or N-type Ca(2+) channels had no major effect. In more mature terminals (postnatal days 14-17), the slow mode of endocytosis was mainly triggered by P/Q-type Ca(2+) channels, suggesting developmental changes in the regulation of the slow mode of endocytosis by different Ca(2+) channel subtypes. In contrast, a fast mode of endocytosis was observed after strong stimulation in young terminals that was mediated mainly by P/Q-type, but not R- or N-type Ca(2+) channels. These results suggest that different types of Ca(2+) channels regulate the two different modes of endocytosis. The results may also suggest that exo- and endocytosis are regulated independently at different sites in young animals but are more tightly coupled in older animals, allowing more efficient synaptic vesicle cycling adapted for fast signalling.
在哺乳动物的中枢突触中,钙离子(Ca(2+))通过钙离子通道内流,触发突触小泡通过胞吐作用释放神经递质,突触小泡与突触前膜融合,随后通过内吞作用回收。在Held终扣处,P/Q型钙离子通道主要介导胞吐作用,而N型和R型通道在幼嫩终扣(出生后第8 - 11天)中作用较小。每种钙离子通道亚型在内吞作用中的作用仍有待阐明;因此,我们结合电容测量技术,使用全细胞膜片钳记录来研究每种类型的钙离子通道在内吞作用中的作用。我们发现,在幼嫩的Held终扣处,当R型钙离子通道被阻断时,内吞作用的慢速模式进一步减慢,而阻断P/Q型或N型钙离子通道则没有主要影响。在更成熟的终扣(出生后第14 - 17天)中,内吞作用的慢速模式主要由P/Q型钙离子通道触发,这表明不同钙离子通道亚型对内吞作用慢速模式的调节存在发育变化。相比之下,在幼嫩终扣受到强烈刺激后观察到一种快速内吞模式,其主要由P/Q型而非R型或N型钙离子通道介导。这些结果表明,不同类型的钙离子通道调节两种不同的内吞模式。这些结果还可能表明,在幼龄动物中,胞吐和内吞在不同位点独立调节,但在老龄动物中耦合更紧密,从而允许更高效的突触小泡循环以适应快速信号传递。