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PMID: 8700210 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Regulation of receptor-mediated endocytosis by Rho and Rac.

Nature ·Vol. 382 ·No. 6587 ·1996-07-11 ·Pages 177-9

Lamaze C, Chuang TH, Terlecky LJ, Bokoch GM, Schmid SL

Abstract

Pinocytosis and membrane ruffling are among the earliest and most dramatic cellular responses to stimulation by growth factors or other mitogens. The small Ras-related G proteins Rho and Rac have a regulatory role in membrane ruffling and activated Rho has been shown to stimulate pinocytosis when microinjected into Xenopus oocytes. In contrast to these well established effects of Rho and Rac on plasma membrane morphology and bulk pinocytosis, there has been no evidence for their involvement in the regulation of receptor-mediated endocytosis in clathrin-coated pits. Here we show that activated Rho and Rac inhibit transferrin-receptor-mediated endocytosis when expressed in intact cells. Furthermore, we have reconstituted these effects in a cell-free system and established that Rho and Rac can regulate clathrin-coated vesicle formation.

MeSH Terms
Cell Line Clathrin/metabolism Coated Vesicles/metabolism Cytochalasin D/pharmacology Endocytosis/drug effects,physiology GTP-Binding Proteins/physiology HeLa Cells Humans Mutation Phalloidine/pharmacology Receptors, Transferrin/antagonists & inhibitors,physiology Recombinant Proteins Transferrin/metabolism rac GTP-Binding Proteins
Chemicals
Clathrin Receptors, Transferrin Recombinant Proteins Transferrin Phalloidine Cytochalasin D GTP-Binding Proteins rac GTP-Binding Proteins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Lamaze C
Department of Cell Biology, The Scripps Research Institute, La Jolla, California 92037, USA.
Chuang T H
Terlecky L J
Bokoch G M
Schmid S L
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1996-07-11
Pages
177-9
Language
English
Region
England
NLM ID
0410462
Subset
IM
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