共 51 条
Focal adhesion kinase: switching between GAPs and GEFs in the regulation of cell motility
被引:186
作者:

Tomar, Alok
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h-index: 0
机构:
Univ Calif San Diego, Dept Reprod Med, Moores Canc Ctr, San Diego, CA 92103 USA Univ Calif San Diego, Dept Reprod Med, Moores Canc Ctr, San Diego, CA 92103 USA

Schlaepfer, David D.
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h-index: 0
机构:
Univ Calif San Diego, Dept Reprod Med, Moores Canc Ctr, San Diego, CA 92103 USA Univ Calif San Diego, Dept Reprod Med, Moores Canc Ctr, San Diego, CA 92103 USA
机构:
[1] Univ Calif San Diego, Dept Reprod Med, Moores Canc Ctr, San Diego, CA 92103 USA
关键词:
RHO-FAMILY GTPASES;
MIGRATING CELLS;
TYROSINE PHOSPHORYLATION;
INTEGRIN ACTIVATION;
MATRIX ADHESIONS;
LEADING-EDGE;
PDZ-RHOGEF;
FAK;
INVASION;
DYNAMICS;
D O I:
10.1016/j.ceb.2009.05.006
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Focal adhesion (FA) kinase (FAK) is a cytoplasmic protein-tyrosine kinase involved in cytoskeleton remodeling, formation and disassembly of cell adhesion structures, and in the regulation of Rho-family GTPases. Therefore, FAK is widely accepted as an important promoter of directional cell movement. Recent studies have elucidated new molecular connections of FAK in these processes. Specifically, FAK facilitates the localized and cyclic activation of guanine nucleotide exchange factors (GEFs) and GTPases-activating proteins (GAPs). In general, GEFs activate, while GAPs inactivate RhoGTPases. Therefore, FAK is in a unique signaling position to modulate RhoGTPase activity in space and time, thereby affecting various steps (integrin activation, leading edge formation, FA turnover, and trailing edge retraction) needed for efficient directional cell migration.
引用
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页码:676 / 683
页数:8
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