Rho-kinase/ROCK is involved in cytokinesis through the phosphorylation of myosin light chain and not ezrin/radixin/moesin proteins at the cleavage furrow

被引:183
作者
Kosako, H
Yoshida, T
Matsumura, F
Ishizaki, T
Narumiya, S
Inagaki, M
机构
[1] Univ Tokyo, Grad Sch Med, Dept Neurobiol, Bunkyo Ku, Tokyo 1130033, Japan
[2] Aichi Canc Ctr, Res Inst, Biochem Lab, Nagoya, Aichi 4648681, Japan
[3] Mie Univ, Sch Med, Dept Pathol, Tsu, Mie 5148507, Japan
[4] Rutgers State Univ, Dept Mol Biol & Biochem, Piscataway, NJ 08855 USA
[5] Kyoto Univ, Fac Med, Dept Pharmacol, Kyoto 6068315, Japan
关键词
cell cycle; cytokinesis; Rho-kinase; myosin light chain; ERM proteins;
D O I
10.1038/sj.onc.1203987
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
The small GTPase Rho and one of its targets, Rho-kinase (also termed ROK or ROCK), are implicated in various cellular functions including stress fiber formation, smooth muscle contraction, tumor cell invasion and cell motility, We have previously reported that Rho-kinase accumulates at the cleavage furrow during cytokinesis in several cultured cells. Here, using Rho-kinase inhibitors, Y-27632 and HA1077, we found that Rho-kinase is responsible for the phosphorylation of myosin regulatory light chain at Ser(19) in the cleavage furrow during cytokinesis. On the other hand, phosphorylation of ezrin/radixin/moesin (ERM) proteins at the cleavage furrow was enhanced by the addition of the above Rho-kinase inhibitors, Treatment with Y-27632 strongly enhanced the accumulation of Rho-kinase but not RhoA and citron kinase at the cleavage furrow. Furthermore, the furrow ingression in cytokinesis was significantly prolonged in the presence of Y-27632, These results suggest that Rho-kinase is involved in the progression of cytokinesis through the phosphorylation of several proteins including myosin light chain at the cleavage furrow.
引用
收藏
页码:6059 / 6064
页数:6
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