Rho kinase in the regulation of cell death and survival

被引:250
作者
Shi, Jianjian [1 ]
Wei, Lei [1 ]
机构
[1] Indiana Univ, Sch Med, Herman B Wells Ctr Pediat Res, Div Pediat Cardiol,Dept Pediat, Indianapolis, IN 46202 USA
关键词
ROCK1; ROCK2; apoptosis; survival; gene targeting;
D O I
10.1007/s00005-007-0009-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Rho kinase (ROCK) belongs to a family of serine/threonine kinases that are activated via interaction with Rho GTPases. ROCK is involved in a wide range of fundamental cellular functions, such as contraction, adhesion, migration, and proliferation. Recent studies have shown that ROCK plays an important role in the regulation of apoptosis in various cell types and animal disease models. Two ROCK isoforms, ROCK1 and ROCK2, are assumed to be function redundant, this based largely on kinase construct overexpression and chemical inhibitors (Y27632 and fasudil) which inhibit both ROCK1 and ROCK2. Gene targeting and RNA interference approaches allow further dissection of distinct cellular, physiological, and patho-physiological functions of the two ROCK isoforms. This review, based on recent molecular, cellular, and animal studies, focuses on the current understanding of ROCK signaling in the regulation of apoptosis and highlights new findings from recently generated ROCK-deficient mice.
引用
收藏
页码:61 / 75
页数:15
相关论文
共 155 条
[1]   Long-term treatment with a Rho-kinase inhibitor improves monocrotaline-induced fatal pulmonary hypertension in rats [J].
Abe, K ;
Shimokawa, H ;
Morikawa, K ;
Uwatoku, T ;
Oi, K ;
Matsumoto, Y ;
Hattori, T ;
Nakashima, Y ;
Kaibuchi, K ;
Sueishi, K ;
Takeshita, A .
CIRCULATION RESEARCH, 2004, 94 (03) :385-393
[2]   Formation of actin stress fibers and focal adhesions enhanced by Rho-kinase [J].
Amano, M ;
Chihara, K ;
Kimura, K ;
Fukata, Y ;
Nakamura, N ;
Matsuura, Y ;
Kaibuchi, K .
SCIENCE, 1997, 275 (5304) :1308-1311
[3]   The COOH terminus of Rho-kinase negatively regulates Rho-kinase activity [J].
Amano, M ;
Chihara, K ;
Nakamura, N ;
Kaneko, T ;
Matsuura, Y ;
Kaibuchi, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (45) :32418-32424
[4]   Phosphorylation and activation of myosin by Rho-associated kinase (Rho-kinase) [J].
Amano, M ;
Ito, M ;
Kimura, K ;
Fukata, Y ;
Chihara, K ;
Nakano, T ;
Matsuura, Y ;
Kaibuchi, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (34) :20246-20249
[5]  
ASANO T, 1987, J PHARMACOL EXP THER, V241, P1033
[6]   Death receptors: Signaling and modulation [J].
Ashkenazi, A ;
Dixit, VM .
SCIENCE, 1998, 281 (5381) :1305-1308
[7]   Loss of cyclophilin D reveals a critical role for mitochondrial permeability transition in cell death [J].
Baines, CP ;
Kaiser, RA ;
Purcell, NH ;
Blair, NS ;
Osinska, H ;
Hambleton, MA ;
Brunskill, EW ;
Sayen, MR ;
Gottlieb, RA ;
Dorn, GW ;
Robbins, J ;
Molkentin, JD .
NATURE, 2005, 434 (7033) :658-662
[8]   Inhibition of Rho-kinase protects the heart against ischemia/reperfusion injury [J].
Bao, WK ;
Hu, E ;
Tao, L ;
Boyce, R ;
Mirabile, R ;
Thudium, DT ;
Ma, XL ;
Willette, RN ;
Yue, TL .
CARDIOVASCULAR RESEARCH, 2004, 61 (03) :548-558
[9]   Active Rho kinase (ROK-α) associates with insulin receptor substrate-1 and inhibits insulin signaling in vascular smooth muscle cells [J].
Begum, N ;
Sandu, OA ;
Ito, M ;
Lohmann, SM ;
Smolenski, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (08) :6214-6222
[10]   Protein kinase a in complex with rho-kinase inhibitors Y-27632, fasudil, and H-1152P: Structural basis of selectivity [J].
Breitenlechner, C ;
Gassel, M ;
Hidaka, H ;
Kinzel, V ;
Huber, R ;
Engh, RA ;
Bossemeyer, D .
STRUCTURE, 2003, 11 (12) :1595-1607