Protein kinase mediators of integrin signal transduction

被引:52
作者
Hannigan, GE
Dedhar, S
机构
[1] HOSP SICK CHILDREN, DIV PATHOL, TORONTO, ON M5G 1X8, CANADA
[2] UNIV TORONTO, DEPT MED BIOPHYS, YORK M4N 3M5, N YORKSHIRE, ENGLAND
[3] SUNNYBROOK HLTH SCI CTR, DIV CANC BIOL RES, YORK M4N 3M5, N YORKSHIRE, ENGLAND
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 1997年 / 75卷 / 01期
基金
英国医学研究理事会;
关键词
protein kinase; integrin; signal transduction; adhesion; oncogenesis;
D O I
10.1007/s001090050084
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Protein kinases are important mediators of signal transduction initiated by soluble growth factors and cytokines. Cellular interactions with the extracellular matrix are mediated largely by members of the integrin class of cell adhesion molecules, which also subsume signal transduction functions required for cell growth, differentiation, and survival. Here we review the involvement of protein kinases in mediating integrin intracellular signal transduction and the possible role for these molecules in regulating integrin adhesion. Although in most cases mechanistic details are incomplete, the emerging theme of protein kinases mediating cross-talk between growth factor receptor and integrin signalling systems provides a timely backdrop against which to present new developments in this area. The contribution of the actin cytoskeleton to integrin signal transduction is discussed, with respect to the concept of 'solid-state' signalling providing a mechanism for imposing order on the protein-protein interactions which underlie signal discrimination. Moreover, we review evidence that dysregulated integrin signalling contributes to pathological processes including arthritis, thrombasthenia, leucocyte adhesion deficiencies, and tumour angiogenesis and invasion.
引用
收藏
页码:35 / 44
页数:10
相关论文
共 116 条
[21]   INTEGRIN PHOSPHORYLATION IS MODULATED DURING THE DIFFERENTIATION OF F9 TERATOCARCINOMA STEM-CELLS [J].
DAHL, SC ;
GRABEL, LB .
JOURNAL OF CELL BIOLOGY, 1989, 108 (01) :183-190
[22]   IDENTIFICATION OF A NOVEL SERINE THREONINE KINASE AND A NOVEL 15-KD PROTEIN AS POTENTIAL MEDIATORS OF THE GAMMA-INTERFERON-INDUCED CELL-DEATH [J].
DEISS, LP ;
FEINSTEIN, E ;
BERISSI, H ;
COHEN, O ;
KIMCHI, A .
GENES & DEVELOPMENT, 1995, 9 (01) :15-30
[23]   SIGNAL-TRANSDUCTION - A TARGET FOR PI(3) KINASE [J].
DOWNWARD, J .
NATURE, 1995, 376 (6541) :553-554
[24]  
EIDE BL, 1995, MOL CELL BIOL, V15, P2819
[25]   ADHESION MOLECULE DEFICIENCIES AND THEIR CLINICAL-SIGNIFICANCE [J].
ETZIONI, A .
CELL ADHESION AND COMMUNICATION, 1994, 2 (03) :257-260
[26]   CONSEQUENCES OF LACK OF BETA-1 INTEGRIN GENE-EXPRESSION IN MICE [J].
FASSLER, R ;
MEYER, M .
GENES & DEVELOPMENT, 1995, 9 (15) :1896-1908
[27]   SHARK, A SRC HOMOLOGY-2, ANKYRIN REPEAT, TYROSINE KINASE, IS EXPRESSED ON THE APICAL SURFACES OF ECTODERMAL EPITHELIA [J].
FERRANTE, AW ;
REINKE, R ;
STANLEY, ER .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (06) :1911-1915
[28]   MECHANISTIC ASPECTS OF NF-KAPPA-B REGULATION - THE EMERGING ROLE OF PHOSPHORYLATION AND PROTEOLYSIS [J].
FINCO, TS ;
BALDWIN, AS .
IMMUNITY, 1995, 3 (03) :263-272
[29]   Interferon-alpha-induced phosphorylation and activation of cytosolic phospholipase A(2) is required for the formation of interferon-stimulated gene factor three [J].
Flati, V ;
Haque, SJ ;
Williams, BRG .
EMBO JOURNAL, 1996, 15 (07) :1566-1571
[30]   THE SUPPRESSOR OF HAIRLESS PROTEIN PARTICIPATES IN NOTCH RECEPTOR SIGNALING [J].
FORTINI, ME ;
ARTAVANISTSAKONAS, S .
CELL, 1994, 79 (02) :273-282