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肌球蛋白II的激活在Rho和Rho激酶作用过程中促进神经突回缩。

Myosin II activation promotes neurite retraction during the action of Rho and Rho-kinase.

作者信息

Amano M, Chihara K, Nakamura N, Fukata Y, Yano T, Shibata M, Ikebe M, Kaibuchi K

机构信息

Division of Signal Transduction, Nara Institute of Science and Technology, Ikoma, Japan.

出版信息

Genes Cells. 1998 Mar;3(3):177-88. doi: 10.1046/j.1365-2443.1998.00181.x.

Abstract

BACKGROUND

The Rho small GTPase regulates myosin II activity through the phosphorylation of the myosin light chain (MLC) by activating Rho-kinase, which is a target of Rho. Several lines of evidence point to an important role of Rho in the action of lysophosphatidic acid (LPA) and thrombin in provoking neurite retraction in N1E-115 neuroblastoma cells.

RESULTS

Here we examined whether Rho-kinase and myosin II are involved in neurite retraction in N1E-115 cells. We showed that the expression of constitutively active forms of Rho-kinase induced neurite retraction in NIE-115 cells and MLC phosphorylation in NIH 3T3 cells, whereas the expression of dominant negative forms of Rho-kinase inhibited the LPA-induced neurite retraction in N1E-115 cells and the serum-induced MLC phosphorylation in NIH 3T3 cells. The expression of mutant MLCT18D,S19D (substitution of Thr and Ser by Asp), which is known to lead to the activation of myosin ATPase and a conformational change of myosin II when reconstituted with myosin heavy chains in vitro, also promoted neurite retraction.

CONCLUSION

These results indicate that Rho-kinase is involved in the LPA-induced neurite retraction downstream of Rho, and that myosin II activation promotes neurite retraction downstream of Rho and Rho-kinase.

摘要

背景

Rho小GTP酶通过激活Rho激酶(Rho的一个靶点)使肌球蛋白轻链(MLC)磷酸化,从而调节肌球蛋白II的活性。多项证据表明,Rho在溶血磷脂酸(LPA)和凝血酶引起N1E - 115神经母细胞瘤细胞神经突回缩的作用中起重要作用。

结果

在此我们研究了Rho激酶和肌球蛋白II是否参与N1E - 115细胞的神经突回缩。我们发现,组成型活性形式的Rho激酶的表达诱导了NIE - 115细胞的神经突回缩以及NIH 3T3细胞中的MLC磷酸化,而显性负性形式的Rho激酶的表达抑制了N1E - 115细胞中LPA诱导的神经突回缩以及NIH 3T3细胞中血清诱导的MLC磷酸化。已知当在体外与肌球蛋白重链重组时会导致肌球蛋白ATP酶激活和肌球蛋白II构象改变的突变型MLCT18D,S19D(苏氨酸和丝氨酸被天冬氨酸取代)的表达也促进了神经突回缩。

结论

这些结果表明,Rho激酶在Rho下游参与LPA诱导的神经突回缩,并且肌球蛋白II激活在Rho和Rho激酶下游促进神经突回缩。

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