Involvement of cell cycle progression in survival signaling through CD40 in the B-lymphocyte line WEHI-231

被引:13
作者
Hirai, H
Adachi, T
Tsubata, T
机构
[1] Tokyo Med & Dent Univ, Sch Biomed Sci, Immunol Lab, Bunkyo Ku, Tokyo 1138510, Japan
[2] Tokyo Med & Dent Univ, Inst Med Res, Dept Immunol, Bunkyo Ku, Tokyo 1138510, Japan
关键词
apoptosis; B lymphocyte; cell cycle progression; CD40; Bcl-xL; A1; p27(kip1);
D O I
10.1038/sj.cdd.4401357
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
The CD40 molecule transmits a signal that abrogates apoptosis induced by ligation of the antigen receptor (BCR) in both primary B cells and B-cell lines such as WEHI-231. Expression of Bcl-xL and A1, antiapoptotic members of the Bcl-2 family, is enhanced by CD40 ligation, and is suggested to mediate CD40-induced B-cell survival. CD40 ligation also promotes cell cycle progression by increasing the levels of cyclin-dependent kinases (CDKs) required for cell cycle progression, and reducing expression of the CDK inhibitor p27(kip1). Here we demonstrate that cell cycle inhibition by retrovirus-mediated p27(kip1) expression does not modulate the levels of Bcl-xL or A1, but significantly reduces the survival of BCR-ligated WEHI-231 cells by CD40 ligation. This indicates that cell cycle progression is crucial for CD40-mediated survival of B cells.
引用
收藏
页码:261 / 269
页数:9
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