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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
p59Hck Isoform Induces F-actin Reorganization to
Form Protrusions of the Plasma Membrane in a Cdc42- and
Rac-dependent Manner*
Sébastien
Carréno,
Emmanuelle
Caron §,
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
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
Fc 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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Copyright © 2002 by the American Society for Biochemistry and Molecular Biology.
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