O'Reilly L A, Huang D C, Strasser A
The Walter and Eliza Hall Institute of Medical Research, PO Royal Melbourne Hospital, Victoria, Australia.
EMBO J. 1996 Dec 16;15(24):6979-90.
The effect of the cell death inhibitor Bcl-2 and its homologues on cell cycle regulation was explored in lymphocytes and cell lines. Expression of a bcl-2 transgene reduced proliferation of thymocytes and delayed cell cycle entry of mitogen-stimulated B and T lymphocytes. Overexpression of Bcl-2, Bcl-xL or adenovirus E1B19kD substantially delayed serum stimulation-induced S phase entry of quiescent NIH 3T3 fibroblasts. Bcl-2-mediated cell survival and growth inhibition are both antagonized by Bax. Bcl-2, Bcl-xL and E1B19kD, but not Bcl-2 mutants that are defective in blocking apoptosis, suppress growth of colon carcinoma cells. This evidence that regulation of cell survival is coupled to control of cell growth has implications for normal cell turnover and tumorigenesis.
在淋巴细胞和细胞系中研究了细胞死亡抑制剂Bcl-2及其同源物对细胞周期调控的影响。bcl-2转基因的表达降低了胸腺细胞的增殖,并延迟了有丝分裂原刺激的B淋巴细胞和T淋巴细胞进入细胞周期。Bcl-2、Bcl-xL或腺病毒E1B19kD的过表达显著延迟了血清刺激诱导的静止NIH 3T3成纤维细胞进入S期。Bax可拮抗Bcl-2介导的细胞存活和生长抑制。Bcl-2、Bcl-xL和E1B19kD,而不是在阻止细胞凋亡方面有缺陷的Bcl-2突变体,可抑制结肠癌细胞的生长。细胞存活调控与细胞生长控制相关的这一证据对正常细胞更新和肿瘤发生具有重要意义。