Non-visual arrestins regulate the focal adhesion formation via small GTPases RhoA and Rac1 independently of GPCRs

被引:14
作者
Cleghorn, Whitney M. [1 ,4 ]
Bulus, Nada [2 ]
Kook, Seunghyi [1 ]
Gurevich, Vsevolod V. [1 ]
Zent, Roy [2 ,3 ]
Gurevich, Eugenia V. [1 ]
机构
[1] Vanderbilt Univ, Dept Pharmacol, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Med, Nashville, TN 37232 USA
[3] Dept Vet Affairs Hosp, Nashville, TN 37232 USA
[4] Univ Washington, Dept Biochem, Seattle, WA 98109 USA
关键词
Arrestin; Small GTPases; RhoA; Rac1; Cell spreading; Cell motility; Actin; Focal adhesions; ACTIN STRESS FIBERS; BETA(2)-ADRENERGIC RECEPTOR; INTEGRIN ENGAGEMENT; BETA-ARRESTINS; CELL-MIGRATION; C-SRC; PROTEIN; ACTIVATION; CDC42; CYTOSKELETON;
D O I
10.1016/j.cellsig.2017.11.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Arrestins recruit a variety of signaling proteins to active phosphorylated G protein-coupled receptors in the plasma membrane and to the cytoskeleton. Loss of arrestins leads to decreased cell migration, altered cell shape, and an increase in focal adhesions. Small GTPases of the Rho family are molecular switches that regulate actin cytoskeleton and affect a variety of dynamic cellular functions including cell migration and cell morphology. Here we show that non-visual arrestins differentially regulate RhoA and Rac1 activity to promote cell spreading via actin reorganization, and focal adhesion formation via two distinct mechanisms. Arrestins regulate these small GTPases independently of G-protein-coupled receptor activation.
引用
收藏
页码:259 / 269
页数:11
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