Hirai H, Adachi T, Tsubata T
Laboratory of Immunology, School of Biomedical Science, and Department of Immunology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
Cell Death Differ. 2004 Mar;11(3):261-9. doi: 10.1038/sj.cdd.4401357.
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.
CD40分子传递一种信号,该信号可消除在原代B细胞和B细胞系(如WEHI-231)中由抗原受体(BCR)连接诱导的细胞凋亡。CD40连接可增强Bcl-2家族的抗凋亡成员Bcl-xL和A1的表达,提示其介导CD40诱导的B细胞存活。CD40连接还通过增加细胞周期进程所需的细胞周期蛋白依赖性激酶(CDK)水平并降低CDK抑制剂p27(kip1)的表达来促进细胞周期进程。在此,我们证明逆转录病毒介导的p27(kip1)表达对细胞周期的抑制作用不会调节Bcl-xL或A1的水平,但会显著降低CD40连接的BCR连接的WEHI-231细胞的存活率。这表明细胞周期进程对于CD40介导的B细胞存活至关重要。