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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Inhibition of neurite extension by overexpression of individual domains of LIM kinase 1.
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Inhibition of neurite extension by overexpression of individual domains of LIM kinase 1.

机译:LIM激酶1单个结构域的过表达抑制神经突延伸。

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摘要

Lin-11, Isl-1 and Mec-3 (LIM) kinases are serine/threonine kinases that phosphorylate cofilin, an actin depolymerizing protein. LIM kinases have a highly modular structure composed of two N-terminal LIM domains (LIM 1/2), a PSD-95, Dlg and ZO-1 (PDZ) domain and a C-terminal protein kinase domain. Here, we overexpressed individual domains of mouse LIM kinase 1 (LIMK1) in PC12 cells and investigated their effects on neurite outgrowth. Although none of the LIMK1 domains had an effect on spontaneous neurite outgrowth, the N-terminal LIM 1/2 domains strongly inhibited differentiation of PC12 cells after stimulation with both nerve growth factor (NGF) and the Rho-kinase inhibitor Y-27632. In contrast, the overexpressed PDZ domain reduced neurite outgrowth only when differentiation had been induced by Y-27632, but not by NGF. Our data suggest that the different non-catalytic N-terminal domains of LIMK1 contribute to the regulation of neurite extension by using distinct signal transduction pathways.
机译:Lin-11,Isl-1和Mec-3(LIM)激酶是丝氨酸/苏氨酸激酶,可磷酸化肌动蛋白解聚蛋白cofilin。 LIM激酶具有高度模块化的结构,该结构由两个N末端LIM域(LIM 1/2),PSD-95,Dlg和ZO-1(PDZ)域和C末端蛋白激酶域组成。在这里,我们在PC12细胞中过表达了小鼠LIM激酶1(LIMK1)的单个域,并研究了它们对神经突生长的影响。尽管没有一个LIMK1结构域对自发性神经突生长有影响,但是在用神经生长因子(NGF)和Rho激酶抑制剂Y-27632刺激后,N末端的LIM 1/2结构域强烈抑制PC12细胞的分化。相反,仅当Y-27632诱导分化但NGF诱导分化时,过表达的PDZ域才减少神经突生长。我们的数据表明,LIMK1的不同非催化性N末端域通过使用不同的信号转导途径有助于神经突延伸的调控。

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