Inhibition of neurite extension by overexpression of individual domains of LIM kinase 1

被引:29
作者
Birkenfeld, J [1 ]
Betz, H [1 ]
Roth, D [1 ]
机构
[1] Max Planck Inst Brain Res, Dept Neurochem, D-60528 Frankfurt, Germany
关键词
actin; cofilin; neurite outgrowth; PC12; cells;
D O I
10.1046/j.1471-4159.2001.00500.x
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
Lin-11, Isf-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, Dig and ZO-1 (PDZ) domain and a C-terminal protein kinase domain. Here, we overexpressed individual domains of mouse LIM kinase I (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 noncatalytic N-terminal domains of LIMK1 contribute to the regulation of neurite extension by using distinct signal transduction pathways.
引用
收藏
页码:924 / 927
页数:4
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