Rab4 regulates formation of synaptic-like microvesicles from early endosomes in PC12 cells

被引:57
作者
de Wit, H
Lichtenstein, Y [1 ]
Kelly, RB
Geuze, HJ
Klumperman, J
van der Sluijs, P
机构
[1] Univ Calif San Francisco, Dept Biochem & Biophys, Hormone Res Inst, San Francisco, CA 94143 USA
[2] Univ Utrecht, Med Ctr, Dept Cell Biol, NL-3584 CX Utrecht, Netherlands
[3] Univ Utrecht, Med Ctr, Inst Biomembranes, NL-3584 CX Utrecht, Netherlands
关键词
D O I
10.1091/mbc.12.11.3703
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Early endosomes in PC12 cells are an important site for the formation of synaptic-like microvesicles and constitutive recycling vesicles. By immunogold electron microscopy, the small GTPase rab4 was localized to early endosomes and numerous small vesicles in the cell periphery and Golgi area of PC12 cells. Overexpression of GTPase-deficient Q67Lrab4 increased the number of early endosome-associated and cytoplasmic vesicles, whereas expression of GDP-bound S22Nrab4 significantly increased the length of early endosomal tubules. In parallel, Q67Lrab4 induced a shift in rab4, VAMP2, and TfR label from early endosomes to peripheral vesicles, whereas S22Nrab4 increased early endosome labeling of all three proteins. These observations were corroborated by early endosome budding assays. Together, our data document a thus far unrecognized role for rab4 in the formation of synaptic-like microvesicles and add to our understanding of the formation of constitutive recycling vesicles from early endosomes.
引用
收藏
页码:3703 / 3715
页数:13
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