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pubmed-article:11694600pubmed:abstractTextEarly 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.lld:pubmed
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pubmed-article:11694600pubmed:authorpubmed-author:KellyR BRBlld:pubmed
pubmed-article:11694600pubmed:authorpubmed-author:GeuzeH JHJlld:pubmed
pubmed-article:11694600pubmed:authorpubmed-author:KlumpermanJJlld:pubmed
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pubmed-article:11694600pubmed:articleTitleRab4 regulates formation of synaptic-like microvesicles from early endosomes in PC12 cells.lld:pubmed
pubmed-article:11694600pubmed:affiliationDepartment of Biochemistry and Biophysics, Hormone Research Institute, University of California, San Francisco, California 94143-0534.lld:pubmed
pubmed-article:11694600pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:11694600pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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