Muris D F R, Verschoor T, Divecha N, Michalides R J A M
Division of Tumour Biology, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, The Netherlands.
Eur J Cancer. 2002 Sep;38(13):1775-82. doi: 10.1016/s0959-8049(02)00100-4.
The Rho-like guanine triphosphate (GTP)ases become activated by extracellular ligands and regulate a wide variety of biological processes, including cell motility, spreading of cells, cytoskeletal organisation and transcriptional activity. We studied the effect of expression of WtRac and Cdc42 and of their constitutive active V12 variants on cell cycle transition using the isopropylthiogalactoside (IPTG) inducible Rac and Cdc42 transfectants of porcine aortic endothelial (PAE) cells. Expression of V12Rac or V12Cdc42 resulted initially in an enrichment of cells in G2/M, followed by the appearance of multinucleated cells with some of the nuclei still being able to incorporate bromodeoxyuridine (BrdU). By fluorescent activated cell sorter (FACS) analysis, these cells appeared as polyploid cells. Prolonged activation of V12Rac or V12Cdc42 resulted in genomic instability and these cells finally detached from the culture plate. These findings indicate that induction of the constitutive active V12 forms of Rac and Cdc42 results in 'mitotic slippage', where endoreplication takes place irrespective of the exit from cytokinesis.
Rho样鸟嘌呤三磷酸(GTP)酶被细胞外配体激活,并调节多种生物学过程,包括细胞运动、细胞铺展、细胞骨架组织和转录活性。我们使用异丙基硫代半乳糖苷(IPTG)诱导猪主动脉内皮(PAE)细胞的Rac和Cdc42转染子,研究了野生型Rac和Cdc42及其组成型活性V12变体的表达对细胞周期转换的影响。V12Rac或V12Cdc42的表达最初导致G2/M期细胞富集增加,随后出现多核细胞,其中一些细胞核仍能掺入溴脱氧尿苷(BrdU)。通过荧光激活细胞分选仪(FACS)分析,这些细胞表现为多倍体细胞。V12Rac或V12Cdc42的长期激活导致基因组不稳定,这些细胞最终从培养板上脱离。这些发现表明,组成型活性V12形式的Rac和Cdc42的诱导导致“有丝分裂滑脱”,即无论胞质分裂是否结束,都会发生核内复制。