The suppression of small GTPase Rho signal transduction pathway inhibits angiogenesis in vitro and in vivo

被引:45
作者
Uchida, S
Watanabe, G
Shimada, Y
Maeda, M
Kawabe, A
Mori, A
Arii, S
Uehata, M
Kishimoto, T
Oikawa, T
Imamura, M
机构
[1] Kyoto Univ, Grad Sch Med, Dept Surg & Surg Basic Sci, Sakyo Ku, Kyoto 6068507, Japan
[2] Yoshitomi Pharmaceut Ind Ltd, Drug Discovery Labs Osaka, Hirakata, Osaka 5731153, Japan
[3] Tottori Univ, Dept Environm Med, Tottori, Japan
[4] Tokyo Metropolitan Inst Med Sci, Dept Canc Therapeut, Tokyo 113, Japan
关键词
D O I
10.1006/bbrc.2000.2315
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
Angiogenesis consists of multistep pathways such as the degradation of the matrix, proliferation of the endothelial cells, motility of the endothelial cells, formation of the cord structure and network formation of microvessels. The small GTPase Rho participates in cell motility through actin fiber polymerization. The role of the small GTPase Rho signal transduction pathway in regulating angiogenesis, however, is still unknown. In this study, we investigated the role of the small GTPase Rho signal transduction pathway in angiogenesis in vitro and in vivo using the exoenzyme, Clostridium botulinum C3 transferase, which specifically suppresses Rho and a compound, Y-27632, which suppresses p160ROCK (Rho-associated coiled-coil containing protein kinase). In this paper, we showed that the small GTPase Rho-p160ROCK signal transduction pathway played an important role in angiogenesis both in vitro and in vivo. These results suggest that inhibition of the small GTPase Rho signal transduction pathway by the p160ROCK inhibitor could be a possible new strategy for angiogenic diseases. (C) 2000 Academic Press.
引用
收藏
页码:633 / 640
页数:8
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