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Cytoplasmic p21Cip1/WAF1 regulates neurite remodeling by inhibiting Rho-kinase activity
被引:128
作者:
Tanaka, H
Yamashita, T
Asada, M
Mizutani, S
Yoshikawa, H
Tohyama, M
机构:
[1] Osaka Univ, Grad Sch Med, Dept Anat & Neurosci, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Grad Sch Med, Dept Orthoped Surg, Suita, Osaka 5650871, Japan
[3] CREST, Japan Sci & Technol Corp, Kawaguchi, Saitama 3320012, Japan
[4] Tokyo Med & Dent Univ, Sch Med, Dept Pediat, Bunkyo Ku, Tokyo 1138519, Japan
关键词:
p21(Cip1/WAF1);
Rho-kinase;
neurite outgrowth;
differentiation;
Rho;
D O I:
10.1083/jcb.200202071
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
(21Cip1/WAF) has cell cycle inhibitory activity by binding to and inhibiting both cyclin/Cdk kinases and proliferating cell nuclear antigen. Here we show that p21(Cip1/WAN) is induced in the cytoplasm during the course of differentiation of chick retinal precursorcells and N1E-115 cells. Ectopic expression of p21(Cip1/WAF1) lacking the nuclear localization signal in N1E-115 cells and NIH3T3 cells affects the formation of actin structures, characteristic of inactivation of Rho. p21(Cip1/WAF1) forms a complex with Rho-kinase and inhibits its activity in vitro and in vivo. Neurite outgrowth and branching from the hippocampal neurons are promoted if p21(Cip1/WAF1) is expressed abundantly in the cytoplasm. These results suggest that cytoplasmic p21(Cip1/WAF1) may contribute to the developmental process of the newborn neurons that extend axons and dendrites into target regions.
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页码:321 / 329
页数:9
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