The effects of the selective ROCK inhibitor, Y27632, on ET-1-induced hypertrophic response in neonatal rat cardiac myocytes - possible involvement of Rho ROCK pathway in cardiac muscle cell hypertrophy

被引:100
作者
Kuwahara, K [1 ]
Saito, Y [1 ]
Nakagawa, O [1 ]
Kishimoto, I [1 ]
Harada, M [1 ]
Ogawa, E [1 ]
Miyamoto, Y [1 ]
Hamanaka, I [1 ]
Kajiyama, N [1 ]
Takahashi, N [1 ]
Izumi, T [1 ]
Kawakami, R [1 ]
Tamura, N [1 ]
Ogawa, Y [1 ]
Nakao, K [1 ]
机构
[1] Kyoto Univ, Grad Sch Med, Dept Med & Clin Sci, Sakyo Ku, Kyoto 606, Japan
来源
FEBS LETTERS | 1999年 / 452卷 / 03期
关键词
endothelin; cardiac hypertrophy; Rho; ROCK; natriuretic peptide;
D O I
10.1016/S0014-5793(99)00680-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A small GTPase, Rho, participates in agonist-induced cytoskeletal organization and gene expression in many cell types including cardiac myocytes, However, little is known about the functions of Rho's downstream targets in cardiac myocytes. We examined the role of ROCK, a downstream target of Rho, in ET-1-induced hypertrophic response. Y27632, a selective ROCK inhibitor, inhibited ET-1-induced increases in natriuretic peptide production, cell size, protein synthesis, and myofibrillar organization. In addition, a dominant-negative mutant of p160ROCK suppressed ET-1-induced transcription of the BNP gene. These findings suggest that the Rho/ROCK pathway is an important component of ET-1-induced hypertrophic signals in cardiac myocytes, (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:314 / 318
页数:5
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