STAT3 orchestrates contradictory signals in cytokine-induced G1 to S cell-cycle transition

被引:219
作者
Fukada, T [1 ]
Ohtani, T [1 ]
Yoshida, Y [1 ]
Shirogane, T [1 ]
Nishida, K [1 ]
Nakajima, K [1 ]
Hibi, M [1 ]
Hirano, T [1 ]
机构
[1] Osaka Univ, Sch Med, Biomed Res Ctr, Div Mol Oncol, Suita, Osaka 5650871, Japan
关键词
cell cycle; cytokine; gp130; signal transduction; STAT3;
D O I
10.1093/emboj/17.22.6670
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 signal transducer and activator of transcription molecules (STATs) play key roles in cytokine-induced signal transduction. However, their role in cell growth has not been clear. In the present study, we show that STAT3 plays a key role in the G(1) to S phase cell-cycle transition induced by the cytokine receptor subunit gp130, through the upregulation of cyclins D2, D3 and A, and cdc25A, and the concomitant downregulation of p21 and p27, Furthermore, unexpectedly, we found that gp130 could induce the expression of p21 when STAT3 activation was suppressed. Such contradictory signals regulating cell-cycle progression could be simultaneously delivered from distinct cytoplasmic regions of gp130, We propose an 'orchestrating model' for cytokine and growth factor action in which contradictory signals are orchestrated to produce a specific effect in a target cell.
引用
收藏
页码:6670 / 6677
页数:8
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