Integrin signalling in neutrophils and macrophages

被引:172
作者
Berton, G [1 ]
Lowell, CA
机构
[1] Univ Verona, Inst Gen Pathol, I-37100 Verona, Italy
[2] Univ Calif San Francisco, Dept Lab Med, San Francisco, CA 94143 USA
关键词
integrin; neutrophil; macrophage; signal transduction; tyrosine kinases;
D O I
10.1016/S0898-6568(99)00003-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Integrins have been characterized extensively as adhesion receptors capable of transducing signals inside the cell. In myelomonocytic cells, integrin-mediated adhesive interactions regulate different selective cell responses, such as transmigration into the inflammatory site, cytokine secretion, production or reactive oxygen intermediates, degranulation and phagocytosis. In the last few years, great progress has been made in elucidating mechanisms of signal transduction by integrins in neutrophils and macrophages. This review summarises the current information on the role of integrins in regulating myelomonocytic cell functions and highlights the signalling pathways activated by integrin engagement in these cells. Also, exploiting the current knowledge of mechanisms of integrin signal transduction in other cell types, we propose a model to explain how integrins transduce signals inside neutrophils and macrophages, and how signaling pathways leading to regulation of selective cell functions may be coordinated. (C) 1999 Elsevier Science Inc.
引用
收藏
页码:621 / 635
页数:15
相关论文
共 235 条
[1]   LIGATED COMPLEMENT RECEPTORS DO NOT ACTIVATE THE ARACHIDONIC-ACID CASCADE IN RESIDENT PERITONEAL-MACROPHAGES [J].
ADEREM, AA ;
WRIGHT, SD ;
SILVERSTEIN, SC ;
COHN, ZA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1985, 161 (03) :617-622
[2]   SPREADING OF DIFFERENTIATING HUMAN MONOCYTES IS ASSOCIATED WITH A MAJOR INCREASE IN MEMBRANE-BOUND CDC42 [J].
AEPFELBACHER, M ;
VAUTI, F ;
WEBER, PC ;
GLOMSET, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (10) :4263-4267
[3]   ADHESION MOLECULES AND INFLAMMATORY INJURY [J].
ALBELDA, SM ;
SMITH, CW ;
WARD, PA .
FASEB JOURNAL, 1994, 8 (08) :504-512
[4]   Molecular definition of distinct cytoskeletal structures involved in complement- and Fc receptor-mediated phagocytosis in macrophages [J].
Allen, LAH ;
Aderem, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (02) :627-637
[5]  
Allen WE, 1997, J CELL SCI, V110, P707
[6]   Granulocyte-macrophage colony-stimulating factor-activated signaling pathways in human neutrophils .1. Tyrosine phosphorylation-dependent stimulation of phosphatidylinositol 3-kinase and inhibition by phorbol esters [J].
AlShami, A ;
Bourgoin, SG ;
Naccache, PH .
BLOOD, 1997, 89 (03) :1035-1044
[7]   OLIGOSPECIFICITY OF THE CELLULAR ADHESION RECEPTOR MAC-1 ENCOMPASSES AN INDUCIBLE RECOGNITION SPECIFICITY FOR FIBRINOGEN [J].
ALTIERI, DC ;
BADER, R ;
MANNUCCI, PM ;
EDGINGTON, TS .
JOURNAL OF CELL BIOLOGY, 1988, 107 (05) :1893-1900
[8]   ADHESIVE RECEPTOR MAC-1 COORDINATES THE ACTIVATION OF FACTOR-X ON STIMULATED CELLS OF MONOCYTIC AND MYELOID DIFFERENTIATION - AN ALTERNATIVE INITIATION OF THE COAGULATION PROTEASE CASCADE [J].
ALTIERI, DC ;
MORRISSEY, JH ;
EDGINGTON, TS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (20) :7462-7466
[9]   ABNORMALITIES OF POLYMORPHONUCLEAR LEUKOCYTE FUNCTION ASSOCIATED WITH A HERITABLE DEFICIENCY OF HIGH MOLECULAR-WEIGHT SURFACE GLYCOPROTEINS (GP138) - COMMON RELATIONSHIP TO DIMINISHED CELL ADHERENCE [J].
ANDERSON, DC ;
SCHMALSTIEG, FC ;
ARNAOUT, MA ;
KOHL, S ;
TOSI, MF ;
DANA, N ;
BUFFONE, GJ ;
HUGHES, BJ ;
BRINKLEY, BR ;
DICKEY, WD ;
ABRAMSON, JS ;
SPRINGER, T ;
BOXER, LA ;
HOLLERS, JM ;
SMITH, CW .
JOURNAL OF CLINICAL INVESTIGATION, 1984, 74 (02) :536-551
[10]  
Astier A, 1997, J BIOL CHEM, V272, P228