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p160 RhoA结合激酶ROKα诱导神经突回缩。

p160 RhoA-binding kinase ROKalpha induces neurite retraction.

作者信息

Katoh H, Aoki J, Ichikawa A, Negishi M

机构信息

Department of Physiological Chemistry, Faculty of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Kyoto 606, Japan.

出版信息

J Biol Chem. 1998 Jan 30;273(5):2489-92. doi: 10.1074/jbc.273.5.2489.

Abstract

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 ROKalpha, a target for RhoA recently identified, on the nerve growth factor-differentiated PC12 cells. Microinjection of the catalytic domain of ROKalpha rapidly induced neurite retraction similar to that induced by microinjection of a constitutively active Rho, RhoV14, whereas microinjection of the kinase-deficient catalytic domain of ROKalpha 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 ROKalpha inhibited the EP3 receptor-induced neurite retraction. These results demonstrate that ROKalpha induces neurite retraction acting downstream of Rho in neuronal cells.

摘要

我们先前报道过,在表达EP3B受体的PC12细胞中,前列腺素E受体EP3亚型的激活通过小GTP酶Rho引起神经突回缩(加藤浩、根岸正、市川明(1996年)《生物化学杂志》271卷,29780 - 29784页)。然而,尚未确定Rho诱导神经突回缩的潜在下游效应物。在此,我们研究了p160 RhoA结合激酶ROKalpha(最近确定的RhoA靶标)对神经生长因子分化的PC12细胞的形态学影响。显微注射ROKalpha的催化结构域能迅速诱导神经突回缩,类似于显微注射组成型活性Rho(RhoV14)所诱导的情况,而显微注射ROKalpha的激酶缺陷型催化结构域则不会诱导神经突回缩。即使预先注射了已知能使Rho失活的C3外切酶,这种形态变化仍能观察到。另一方面,显微注射ROKalpha的Rho结合结构域或普列克底物蛋白同源结构域可抑制EP3受体诱导的神经突回缩。这些结果表明,ROKalpha在神经元细胞中作为Rho的下游发挥作用,诱导神经突回缩。

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