Nakata T, Terada S, Hirokawa N
Department of Cell Biology and Anatomy, Graduate School of Medicine, University of Tokyo, Hongo, Tokyo, Japan, 113.
J Cell Biol. 1998 Feb 9;140(3):659-74. doi: 10.1083/jcb.140.3.659.
Newly synthesized membrane proteins are transported by fast axonal flow to their targets such as the plasma membrane and synaptic vesicles. However, their transporting vesicles have not yet been identified. We have successfully visualized the transporting vesicles of plasma membrane proteins, synaptic vesicle proteins, and the trans-Golgi network residual proteins in living axons at high resolution using laser scan microscopy of green fluorescent protein-tagged proteins after photobleaching. We found that all of these proteins are transported by tubulovesicular organelles of various sizes and shapes that circulate within axons from branch to branch and switch the direction of movement. These organelles are distinct from the endosomal compartments and constitute a new entity of membrane organelles that mediate the transport of newly synthesized proteins from the trans-Golgi network to the plasma membrane.
新合成的膜蛋白通过快速轴突运输到达其靶点,如质膜和突触小泡。然而,它们的运输小泡尚未被识别。我们利用光漂白后绿色荧光蛋白标记蛋白的激光扫描显微镜,成功地在高分辨率下可视化了活轴突中质膜蛋白、突触小泡蛋白和反式高尔基体网络残留蛋白的运输小泡。我们发现,所有这些蛋白都由各种大小和形状的管状小泡细胞器运输,这些细胞器在轴突内从一个分支循环到另一个分支,并改变运动方向。这些细胞器与内体区室不同,构成了一种新的膜细胞器实体,介导新合成蛋白从反式高尔基体网络向质膜的运输。