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Stat3依赖性诱导M1小鼠骨髓白血病细胞中的BATF

Stat3-dependent induction of BATF in M1 mouse myeloid leukemia cells.

作者信息

Senga Takeshi, Iwamoto Takashi, Humphrey Sean E, Yokota Takashi, Taparowsky Elizabeth J, Hamaguchi Michinari

机构信息

Department of Molecular Pathogenesis, Nagoya University School of Medicine, 65 Tsurumai Showa Nagoya 466-8550, Japan.

出版信息

Oncogene. 2002 Nov 21;21(53):8186-91. doi: 10.1038/sj.onc.1205918.

Abstract

Stat3 mediates cellular responses associated with proliferation, survival and differentiation, but the mechanisms underlying the diverse effects of this signaling molecule remain unknown. M1 mouse myeloid leukemia cells arrest growth and differentiate into macrophages following treatment with interleukin 6 (IL-6) or leukemia inhibitory factor (LIF), and recent studies have shown that Stat3 plays a central role in this process. Utilizing representational difference analysis, we demonstrate that expression of the mouse BATF gene is upregulated as an early response to IL-6/LIF stimulation and Stat3 activation in this cell system. Immunoblots using antibodies to BATF detected an increase in BATF protein in response to LIF/IL-6 stimulation. BATF is a member of the AP-1 family of basic leucine zipper transcription factors and functions to inhibit the transcriptional and biological functions of AP-1 activity in mammalian cells. BATF forms complexes with c-Jun in M1 cells and forced expression of BATF in the absence of Stat3 signaling results in a reduced rate of cellular growth. These results indicate that Stat3 mediates cellular growth by modulating AP-1 activity through the induction of BATF.

摘要

信号转导和转录激活因子3(Stat3)介导与细胞增殖、存活及分化相关的细胞反应,但是这种信号分子产生多种效应的潜在机制仍不清楚。用白细胞介素6(IL-6)或白血病抑制因子(LIF)处理后,M1小鼠髓系白血病细胞会停止生长并分化为巨噬细胞,最近的研究表明Stat3在此过程中起核心作用。利用代表性差异分析,我们证明在该细胞系统中,小鼠BATF基因的表达作为对IL-6/LIF刺激和Stat3激活的早期反应而被上调。使用针对BATF的抗体进行免疫印迹检测到,响应LIF/IL-6刺激,BATF蛋白增加。BATF是碱性亮氨酸拉链转录因子AP-1家族的成员,其功能是在哺乳动物细胞中抑制AP-1活性的转录和生物学功能。在M1细胞中,BATF与c-Jun形成复合物,并且在不存在Stat3信号传导的情况下强制表达BATF会导致细胞生长速率降低。这些结果表明,Stat3通过诱导BATF来调节AP-1活性,从而介导细胞生长。

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