Faculty of Pharmacy, Iwakimeisei University, Chuoudai, Iwaki, Japan.
Eur J Neurosci. 2010 Aug;32(3):335-46. doi: 10.1111/j.1460-9568.2010.07300.x.
Endocytosis at the presynaptic terminal is initiated by Ca(2+) influx through voltage-gated Ca(2+) channels. At the Drosophila neuromuscular junction, we demonstrated two components of endocytosis linked to distinct Ca(2+) channels. A voltage-gated Ca(2+) channel blocker, (R)-(+)-Bay K8644 (R-BayK), selectively blocked one component (R-BayK-sensitive component) without affecting exocytosis, while low concentrations of La(3+) preferentially depressed the other component (La(3+) -sensitive component). In a temperature-sensitive mutant, shibire(ts), at non-permissive temperatures, dynamin clusters were found immunohistochemically at the active zone (AZ) during the R-BayK-sensitive endocytosis, while they were detected at the non-AZ during the La(3+)-sensitive endocytosis. Immunostaining of the Ca(2+) channel alpha(2)delta subunit encoded by straightjacket (stj) was found within the AZ, and a mutation in stj depressed the R-BayK-sensitive component but enhanced the La(3+) -sensitive one, indicating that the alpha(2)delta subunit is associated with the R-BayK-sensitive Ca(2+) channel. Filipin bound to the non-AZ membrane and inhibited the La(3+) -sensitive component, but not the R-BayK-sensitive one. We concluded that the R-BayK-sensitive component of endocytosis occurred at the AZ and termed this AZ endocytosis. We also concluded that the La(3+) -sensitive component occurred at the non-AZ and termed this non-AZ endocytosis. These two types of endocytosis were modulated by various drugs towards opposite directions, indicating that they were differentially regulated. During high-frequency stimulation, AZ endocytosis operated mainly in the early phase, whereas non-AZ endocytosis operated in the late phase. Thus, intense synaptic transmission is coordinately maintained by synaptic vesicle recycling initiated by Ca(2+) influx through the two types of Ca(2+) channel.
突触前末梢的内吞作用是由电压门控钙离子通道的钙离子内流引发的。在果蝇的神经肌肉接点,我们证明了与两种不同钙离子通道相联系的内吞作用的两个组成部分。电压门控钙离子通道阻断剂(R)-(+)-Bay K8644(R-BayK),选择性地阻断一个组成部分(R-BayK 敏感成分)而不影响胞吐作用,而低浓度的镧(La)优先抑制另一个组成部分(La 敏感成分)。在温度敏感突变体 shibire(ts)中,在非许可温度下,在用 R-BayK 敏感内吞作用时,在活性区(AZ)处用免疫组织化学法发现了动力蛋白簇,而在用 La 敏感内吞作用时,在非-AZ 处发现了动力蛋白簇。在直筒夹克(stj)编码的钙离子通道的 alpha2delta 亚基上的免疫染色在 AZ 内被发现,并且在 stj 中的突变降低了 R-BayK 敏感的成分,但增强了 La 敏感的成分,表明 alpha2delta 亚基与 R-BayK 敏感的钙离子通道有关。鬼笔环肽结合到非-AZ 膜上并抑制了 La 敏感的成分,但不抑制 R-BayK 敏感的成分。我们得出结论,内吞作用的 R-BayK 敏感成分发生在 AZ 中,并称这种内吞作用为 AZ 内吞作用。我们还得出结论,La 敏感的成分发生在非-AZ 中,并称这种内吞作用为非-AZ 内吞作用。这两种类型的内吞作用被各种药物以相反的方向调节,表明它们受到不同的调节。在高频刺激期间,AZ 内吞作用主要在早期阶段起作用,而非-AZ 内吞作用在晚期阶段起作用。因此,强烈的突触传递通过钙离子内流通过两种类型的钙离子通道引发的突触小泡再循环而被协调地维持。