Cytoplasmic p21Cip1/WAF1 regulates neurite remodeling by inhibiting Rho-kinase activity

Author:

Tanaka Hiroyuki123,Yamashita Toshihide13,Asada Minoru4,Mizutani Shuki4,Yoshikawa Hideki2,Tohyama Masaya13

Affiliation:

1. Department of Anatomy and Neuroscience, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan

2. Department of Orthopedic Surgery, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan

3. CREST, Japan Science and Technology Corporation, Kawaguchi, Saitama 332-0012, Japan

4. Department of Pediatrics, Tokyo Medical and Dental University School of Medicine, Bunkyo-Ku, Tokyo 113-8519, Japan

Abstract

p21Cip1/WAF1 has cell cycle inhibitory activity by binding to and inhibiting both cyclin/Cdk kinases and proliferating cell nuclear antigen. Here we show that p21Cip1/WAF1 is induced in the cytoplasm during the course of differentiation of chick retinal precursor cells and N1E-115 cells. Ectopic expression of p21Cip1/WAF1 lacking the nuclear localization signal in N1E-115 cells and NIH3T3 cells affects the formation of actin structures, characteristic of inactivation of Rho. p21Cip1/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 p21Cip1/WAF1 is expressed abundantly in the cytoplasm. These results suggest that cytoplasmic p21Cip1/WAF1 may contribute to the developmental process of the newborn neurons that extend axons and dendrites into target regions.

Publisher

Rockefeller University Press

Subject

Cell Biology

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