Yamashita Takayuki, Hige Toshihide, Takahashi Tomoyuki
Department of Neurophysiology, University of Tokyo Graduate School of Medicine, Tokyo 113-0033, Japan.
Science. 2005 Jan 7;307(5706):124-7. doi: 10.1126/science.1103631.
Molecular dependence of vesicular endocytosis was investigated with capacitance measurements at the calyx of Held terminal in brainstem slices. Intraterminal loading of botulinum toxin E revealed that the rapid capacitance transient implicated as "kiss-and-run" was unrelated to transmitter release. The release-related capacitance change decayed with an endocytotic time constant of 10 to 25 seconds, depending on the magnitude of exocytosis. Presynaptic loading of the nonhydrolyzable guanosine 5'-triphosphate (GTP) analog GTPgS or dynamin-1 proline-rich domain peptide abolished endocytosis. These compounds had no immediate effect on exocytosis, but caused a use-dependent rundown of exocytosis. Thus, the guanosine triphosphatase dynamin-1 is indispensable for vesicle endocytosis at this fast central nervous system (CNS) synapse.
利用脑干切片中Held终扣处的电容测量法,研究了囊泡内吞作用的分子依赖性。肉毒杆菌毒素E的终扣内加载显示,被认为是“亲吻-逃离”的快速电容瞬变与神经递质释放无关。与释放相关的电容变化以10至25秒的内吞时间常数衰减,这取决于胞吐作用的幅度。不可水解的鸟苷5'-三磷酸(GTP)类似物GTPγS或富含脯氨酸结构域的发动蛋白-1肽的突触前加载消除了内吞作用。这些化合物对胞吐作用没有立即影响,但导致了胞吐作用的使用依赖性减少。因此,鸟苷三磷酸酶发动蛋白-1对于这个快速中枢神经系统(CNS)突触处的囊泡内吞作用是不可或缺的。