A central role for Stat3 in IL-6-induced regulation of growth and differentiation in M1 leukemia cells

被引:520
作者
Nakajima, K [1 ]
Yamanaka, Y [1 ]
Nakae, K [1 ]
Kojima, H [1 ]
Ichiba, M [1 ]
Kiuchi, N [1 ]
Kitaoka, T [1 ]
Fukada, T [1 ]
Hibi, M [1 ]
Hirano, T [1 ]
机构
[1] OSAKA UNIV, SCH MED, BIOMED RES CTR, DEPT MOLEC ONCOL, SUITA, OSAKA 565, JAPAN
关键词
differentiation; growth arrest; interleukin; 6; M1; Stat3;
D O I
10.1002/j.1460-2075.1996.tb00734.x
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
Interleukin-6 (IL-6) induces either differentiation or growth of a variety of cells. Little is known about the molecular basis of this cellular decision. The family of signal transducer and activator of transcription (Stat) proteins are involved in signaling through a variety of cytokine and growth factor receptors, although their biological roles have not been established. To address whether Stat proteins play roles in IL-6-induced growth or differentiation, we introduced two types of mutant Stat3 acting in a dominant-negative manner into M1 leukemic cells which respond to IL-6 with growth arrest and terminal differentiation. We show that dominant-negative forms of Stat3 inhibited both IL-6-induced growth arrest at G(0)/G(1) and macrophage differentiation in the M1 transformants. Blocking of Stat activation resulted in inhibition of IL-6-induced repression of c-myb and c-myc. Furthermore, IL-6 enhanced the growth of M1 cells primarily through shortening the length of the G(1) period when Stat3 was suppressed. Thus IL-6 generates both growth-enhancing signals and growth arrest- and differentiation-inducing signals at the same time. Stat3 may be a key molecule which determines the cellular decision from cell growth to differentiation in M1 cells.
引用
收藏
页码:3651 / 3658
页数:8
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