Watanabe Shigeki, Trimbuch Thorsten, Camacho-Pérez Marcial, Rost Benjamin R, Brokowski Bettina, Söhl-Kielczynski Berit, Felies Annegret, Davis M Wayne, Rosenmund Christian, Jorgensen Erik M
Department of Biology and Howard Hughes Medical Institute, University of Utah, Salt Lake City, Utah 84112-0840, USA.
Neuroscience Research Center Charité Universitätsmedizin Berlin, Berlin 10117, Germany.
Nature. 2014 Nov 13;515(7526):228-33. doi: 10.1038/nature13846. Epub 2014 Oct 8.
Ultrafast endocytosis can retrieve a single, large endocytic vesicle as fast as 50-100 ms after synaptic vesicle fusion. However, the fate of the large endocytic vesicles is not known. Here we demonstrate that these vesicles transition to a synaptic endosome about one second after stimulation. The endosome is resolved into coated vesicles after 3 s, which in turn become small-diameter synaptic vesicles 5-6 s after stimulation. We disrupted clathrin function using RNA interference (RNAi) and found that clathrin is not required for ultrafast endocytosis but is required to generate synaptic vesicles from the endosome. Ultrafast endocytosis fails when actin polymerization is disrupted, or when neurons are stimulated at room temperature instead of physiological temperature. In the absence of ultrafast endocytosis, synaptic vesicles are retrieved directly from the plasma membrane by clathrin-mediated endocytosis. These results may explain discrepancies among published experiments concerning the role of clathrin in synaptic vesicle endocytosis.
超快速内吞作用能够在突触小泡融合后50 - 100毫秒内迅速回收单个大的内吞小泡。然而,这些大的内吞小泡的命运尚不清楚。在此我们证明,这些小泡在刺激后约一秒转变为突触内体。内体在3秒后分解为被膜小泡,而这些被膜小泡在刺激后5 - 6秒又转变为小直径的突触小泡。我们利用RNA干扰(RNAi)破坏网格蛋白的功能,发现网格蛋白对于超快速内吞作用并非必需,但对于从内体生成突触小泡却是必需的。当肌动蛋白聚合被破坏时,或者当神经元在室温而非生理温度下受到刺激时,超快速内吞作用就会失败。在没有超快速内吞作用的情况下,突触小泡通过网格蛋白介导的内吞作用直接从质膜回收。这些结果可能解释了已发表实验中关于网格蛋白在突触小泡内吞作用中作用的差异。