p160 RhoA-binding kinase ROKα induces neurite retraction

被引:166
作者
Katoh, H
Aoki, J
Ichikawa, A
Negishi, M [1 ]
机构
[1] Kyoto Univ, Fac Pharmaceut Sci, Dept Mol Neurobiol, Sakyo Ku, Kyoto 606, Japan
[2] Kyoto Univ, Fac Pharmaceut Sci, Dept Physiol Chem, Sakyo Ku, Kyoto 606, Japan
关键词
D O I
10.1074/jbc.273.5.2489
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
We previously reported that the activation of prostaglandin E receptor EP3 subtype caused neurite retraction via small GTPase Rho in the EP3B receptor-expressing PC12 cells (Katoh, H., Negishi, M., and Ichikawa, A. (1996) J. Biol. Chem. 271, 29780-29784). However, a potential downstream effector of Rho that induces neurite retraction was not identified, Here we examined the morphological effect of p160 RhoA-binding kinase ROK alpha, a target for RhoA recently identified, on the nerve growth factor-differentiated PC12 cells. Microinjection of the catalytic domain of ROK alpha rapidly induced neurite retraction similar to that induced by microinjection of a constitutively active Rho, Rho(V14) whereas microinjection of the kinase-deficient catalytic domain of ROK alpha did not induce neurite retraction. This morphological change was observed even though C3 exoenzyme, which was known to inactivate Rho, had been preinjected. On the other hand, microinjection of the Rho-binding domain or the pleckstrin homology domain of ROK alpha inhibited the EP3 receptor-induced neurite retraction, These results demonstrate that ROK alpha induces neurite retraction acting downstream of Rho in neuronal cells.
引用
收藏
页码:2489 / 2492
页数:4
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