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Originally published In Press as doi:10.1074/jbc.M201212200 on March 19, 2002

J. Biol. Chem., Vol. 277, Issue 23, 21007-21016, June 7, 2002
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p59Hck Isoform Induces F-actin Reorganization to Form Protrusions of the Plasma Membrane in a Cdc42- and Rac-dependent Manner*

Sébastien Carréno, Emmanuelle CaronDagger §, Céline Cougoule, Laurent J. Emorine, and Isabelle Maridonneau-Parini||

From the Institut de Pharmacologie et de Biologie Structurale, Centre National de la Recherche Scientifique UMR 5089, 205 route de Narbonne, Toulouse cedex 31077, France and Dagger  Medical Research Council Laboratory for Molecular Cell Biology, CRC Oncogene and Signal Transduction Group, University College London, Gower Street, London WC1E 6BT, United Kingdom

Hck is a protein kinase of the Src family specifically expressed in phagocytes as two isoforms, p59Hck and p61Hck, localized at the plasma membrane and lysosomes, respectively. Their individual involvement in functions ascribed to Hck, phagocytosis, cell migration, and lysosome mobilization, is still unclarified. To investigate the specific role of p59Hck, a constitutively active variant in fusion with green fluorescent protein (p59Hckca) was expressed in HeLa cells. p59Hckca was found at focal adhesion sites and triggered reorganization of the actin cytoskeleton, leading to plasma membrane protrusions where it co-localized with F-actin. Similarly, microinjection of p59Hckca cDNA in J774.A1 macrophages induced membrane protrusions. Whereas kinase activity and membrane association of p59Hck were dispensable for location at focal adhesions, p59Hck-induced membrane protrusions were dependent on kinase activity, plasma membrane association, and Src homology 2 but not Src homology 3 domain and were inhibited by dominant-negative forms of Cdc42 or Rac but not by blocking Rho activity. A dominant negative form of p59Hck inhibited the Cdc42- and Rac-dependent Fcgamma RIIa-mediated phagocytosis. Expression of the Cdc42/Rac-interacting domain of p21-activated kinase in macrophages abolished the p59Hckca-induced morphological changes. Therefore, p59Hck-triggered remodeling of the actin cytoskeleton depends upon the activity of Cdc42 and Rac to promote formation of membrane protrusions necessary for phagocytosis and cell migration.


* This work was supported in part by Sidaction (don 375), Association pour la Recherche contre le Cancer, and European Community Grant QLK2CT19990193.The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

§ Supported by the Wellcome Trust. Present address: Center for Molecular Microbiology and Infection and Dept. of Biological Sciences, Imperial College of Science, Technology and Medicine, The Flowers Bldg., Armstrong Rd., London SW7 2AZ, UK.

Present address: LBCMCP-CNRS, Toulouse 31077, France.

|| To whom correspondence should be addressed. Tel.: 33-5-61175458; Fax: 33-5-61175994; E-mail: maridono@ipbs.fr.


Copyright © 2002 by The American Society for Biochemistry and Molecular Biology, Inc.
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