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PMID: 9348306 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Requirements for both Rac1 and Cdc42 in membrane ruffling and phagocytosis in leukocytes.

The Journal of experimental medicine ·Vol. 186 ·No. 9 ·1997-11-03 ·Pages 1487-94

Cox D, Chang P, Zhang Q, Reddy PG, Bokoch GM, Greenberg S

Abstract

Specific pathways linking heterotrimeric G proteins and Fcgamma receptors to the actin-based cytoskeleton are poorly understood. To test a requirement for Rho family members in cytoskeletal events mediated by structurally diverse receptors in leukocytes, we transfected the full-length human chemotactic peptide receptor in RAW 264.7 cells and examined cytoskeletal alterations in response to the chemotactic peptide formyl-methionyl-leucyl-phenylalanine (FMLP), colony stimulating factor-1 (CSF-1), IgG-coated particles, and phorbol 12-myristate 13-acetate (PMA). Expression of Rac1 N17, Cdc42 N17, or the GAP domain of n-chimaerin inhibited cytoskeletal responses to FMLP and CSF-1, and blocked phagocytosis. Accumulation of F-actin- rich "phagocytic cups" was partially inhibited by expression of Rac1 N17 or Cdc42 N17. In contrast, PMA-induced ruffling was not inhibited by expression of Rac1 N17, but was blocked by expression of Cdc42 N17, indicating that cytoskeletal inhibition by these constructs was nonoverlapping. These results demonstrate differential requirements for Rho family GTPases in leukocyte motility, and indicate that both Rac1 and Cdc42 are required for Fcgamma receptor- mediated phagocytosis and for membrane ruffling mediated by structurally distinct receptors in macrophages.

MeSH Terms
Animals Cell Cycle Proteins/biosynthesis,genetics,physiology Cell Line Cell Membrane/drug effects,physiology Cell Movement/drug effects Chimerin 1 Cytoskeleton/drug effects,physiology GTP Phosphohydrolases/biosynthesis,genetics GTP-Binding Proteins/biosynthesis,genetics,physiology GTPase-Activating Proteins Humans Macrophage Colony-Stimulating Factor/pharmacology Macrophages/metabolism,physiology Mice N-Formylmethionine Leucyl-Phenylalanine/metabolism,pharmacology Nerve Tissue Proteins/pharmacology Phagocytosis/drug effects Proteins/pharmacology Receptors, Formyl Peptide Receptors, IgG/physiology Receptors, Immunologic/biosynthesis Receptors, Peptide/biosynthesis Tetradecanoylphorbol Acetate/pharmacology Transfection rac GTP-Binding Proteins
Chemicals
Cell Cycle Proteins Chimerin 1 GTPase-Activating Proteins Nerve Tissue Proteins Proteins Receptors, Formyl Peptide Receptors, IgG Receptors, Immunologic Receptors, Peptide N-Formylmethionine Leucyl-Phenylalanine Macrophage Colony-Stimulating Factor GTP Phosphohydrolases GTP-Binding Proteins rac GTP-Binding Proteins Tetradecanoylphorbol Acetate
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Cox D
Pulmonary Division, Department of Medicine, Columbia University College of Physicians and Surgeons, New York 10032, USA.
Chang P
Zhang Q
Reddy P G
Bokoch G M
Greenberg S
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1997-11-03
Pages
1487-94
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2199122
Subset
IM
Grants
NIGMS NIH HHS · GM-44428 · United States
NHLBI NIH HHS · HL-54164 · United States
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