Protein kinase mediators of integrin signal transduction
被引:52
作者:
Hannigan, GE
论文数: 0引用数: 0
h-index: 0
机构:HOSP SICK CHILDREN, DIV PATHOL, TORONTO, ON M5G 1X8, CANADA
Hannigan, GE
Dedhar, S
论文数: 0引用数: 0
h-index: 0
机构:HOSP SICK CHILDREN, DIV PATHOL, TORONTO, ON M5G 1X8, CANADA
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.
机构:
TECHNION ISRAEL INST TECHNOL,BRUCE RAPPAPORT FAC MED,RAMBAM MED CTR,DEPT CLIN IMMUNOL,IL-31096 HAIFA,ISRAELTECHNION ISRAEL INST TECHNOL,BRUCE RAPPAPORT FAC MED,RAMBAM MED CTR,DEPT CLIN IMMUNOL,IL-31096 HAIFA,ISRAEL
机构:
YESHIVA UNIV ALBERT EINSTEIN COLL MED, DEPT DEV & MOLEC BIOL, BRONX, NY 10461 USAYESHIVA UNIV ALBERT EINSTEIN COLL MED, DEPT DEV & MOLEC BIOL, BRONX, NY 10461 USA
FERRANTE, AW
;
REINKE, R
论文数: 0引用数: 0
h-index: 0
机构:
YESHIVA UNIV ALBERT EINSTEIN COLL MED, DEPT DEV & MOLEC BIOL, BRONX, NY 10461 USAYESHIVA UNIV ALBERT EINSTEIN COLL MED, DEPT DEV & MOLEC BIOL, BRONX, NY 10461 USA
REINKE, R
;
STANLEY, ER
论文数: 0引用数: 0
h-index: 0
机构:
YESHIVA UNIV ALBERT EINSTEIN COLL MED, DEPT DEV & MOLEC BIOL, BRONX, NY 10461 USAYESHIVA UNIV ALBERT EINSTEIN COLL MED, DEPT DEV & MOLEC BIOL, BRONX, NY 10461 USA
机构:
TECHNION ISRAEL INST TECHNOL,BRUCE RAPPAPORT FAC MED,RAMBAM MED CTR,DEPT CLIN IMMUNOL,IL-31096 HAIFA,ISRAELTECHNION ISRAEL INST TECHNOL,BRUCE RAPPAPORT FAC MED,RAMBAM MED CTR,DEPT CLIN IMMUNOL,IL-31096 HAIFA,ISRAEL
机构:
YESHIVA UNIV ALBERT EINSTEIN COLL MED, DEPT DEV & MOLEC BIOL, BRONX, NY 10461 USAYESHIVA UNIV ALBERT EINSTEIN COLL MED, DEPT DEV & MOLEC BIOL, BRONX, NY 10461 USA
FERRANTE, AW
;
REINKE, R
论文数: 0引用数: 0
h-index: 0
机构:
YESHIVA UNIV ALBERT EINSTEIN COLL MED, DEPT DEV & MOLEC BIOL, BRONX, NY 10461 USAYESHIVA UNIV ALBERT EINSTEIN COLL MED, DEPT DEV & MOLEC BIOL, BRONX, NY 10461 USA
REINKE, R
;
STANLEY, ER
论文数: 0引用数: 0
h-index: 0
机构:
YESHIVA UNIV ALBERT EINSTEIN COLL MED, DEPT DEV & MOLEC BIOL, BRONX, NY 10461 USAYESHIVA UNIV ALBERT EINSTEIN COLL MED, DEPT DEV & MOLEC BIOL, BRONX, NY 10461 USA