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Volume 271, Number 46, Issue of November 15, 1996 pp. 29191-29197
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.

Rab4 and Rab7 Define Distinct Nonoverlapping Endosomal Compartments

(Received for publication, November 14, 1995, and in revised form, April 12, 1996)

Gina Bottger , Bas Nagelkerken and Peter van der Sluijs

From the Department of Cell Biology, Utrecht University School of Medicine, Heidelberglaan 100, 3584 CX Utrecht, The Netherlands

Several Rab GTPases have been localized to distinct compartments of the endocytic pathway. Rab4 is associated with early endosomes and recycling vesicles and regulates membrane recycling from early endosomes. Rab7 is localized to late endosomes and is involved in the regulation of membrane transport between late endosomes and lysosomes. Although Rab4 and Rab7 appear to regulate distinct transport events in endocytosis, it is not clear whether they perform their activities in related or entirely distinct intracellular compartments. To address this question, we generated stable cell lines expressing Rab4 tagged with a novel X31 influenza hemagglutinin (NH) epitope tag. These antibodies are characterized in this paper and were used to immunoisolate endocytic vesicles with cytoplasmically exposed NHRab4. Immunoisolated membranes contain internalized 125I-transferrin, but are devoid of Rab7. Confocal immunofluorescence microscopy showed that the early endosomal GTPases Rab4 and Rab5 both do not codistribute with Rab7 within the same cell. These observations suggest that each of the three Rab GTPases operationally defines a distinct station of the endocytic pathway.


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