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FoxM1, a Forkhead Transcription Factor Is a Master Cell Cycle Regulator for Mouse Mature T Cells but Not Double Positive Thymocytes

机译:FoxM1,一个叉头转录因子是小鼠成熟T细胞但不是双阳性胸腺细胞的主细胞周期调节剂

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FoxM1 is a forkhead box transcription factor and a known master regulator required for different phases of the cell cycle. In cell lines, FoxM1 deficient cells exhibit delayed S phase entry, aneuploidy, polyploidy and can't complete mitosis. In vivo, FoxM1 is expressed mostly in proliferating cells but is surprisingly also found in non-proliferating CD4+CD8+ double positive thymocytes. Here, we addressed the role of FoxM1 in T cell development by generating and analyzing two different lines of T-cell specific FoxM1 deficient mice. As expected, FoxM1 is required for proliferation of early thymocytes and activated mature T cells. Defective expression of many cell cycle proteins was detected, including cyclin A, cyclin B1, cdc2, cdk2, p27 and the Rb family members p107 and p130 but surprisingly not survivin. Unexpectedly, loss of FoxM1 only affects a few cell cycle proteins in CD4+CD8+ thymocytes and has little effect on their sensitivity to apoptosis and the subsequent steps of T cell differentiation. Thus, regulation of cell cycle genes by FoxM1 is stage- and context-dependent.
机译:FoxM1是叉头盒转录因子,是细胞周期不同阶段所需的已知主调节剂。在细胞系中,FoxM1缺陷细胞表现出延迟的S期进入,非整倍性,多倍性,并且不能完成有丝分裂。在体内,FoxM1主要在增殖细胞中表达,但令人惊讶的是,在非增殖CD4 + CD8 +双阳性胸腺细胞中也发现了FoxM1。在这里,我们通过生成和分析两种不同的T细胞特异性FoxM1缺陷小鼠系来解决FoxM1在T细胞发育中的作用。如预期的那样,FoxM1是早期胸腺细胞和活化的成熟T细胞增殖所必需的。检测到许多细胞周期蛋白的缺陷表达,包括细胞周期蛋白A,细胞周期蛋白B1,cdc2,cdk2,p27和Rb家族成员p107和p130,但令人惊讶的是未发现survivin。出乎意料的是,FoxM1的丢失仅影响CD4 + CD8 +胸腺细胞中的一些细胞周期蛋白,而对它们对细胞凋亡的敏感性以及随后的T细胞分化步骤几乎没有影响。因此,FoxM1对细胞周期基因的调节是阶段和上下文相关的。

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