作者
Masashi Minami, Masahiro Inoue, Shi Wei, Kiyoshi Takeda, Makoto Matsumoto, Tadamitsu Kishimoto, Shizuo Akira
发表日期
1996/4/30
期刊
Proceedings of the National Academy of Sciences
卷号
93
期号
9
页码范围
3963-3966
简介
Myeloid leukemia M1 cells can be induced for growth arrest and terminal differentiation into macrophages in response to interleukin 6 (IL-6) or leukemia inhibitory factor (LIF). Recently, a large number of cytokines and growth factors have been shown to activate the Janus kinase (JAK)-signal transducer and activator of transcription (STAT) signaling pathway. In the case of IL-6 and LIF, which share a signal transducing receptor gp130, STAT3 is specifically tyrosine-phosphorylated and activated by stimulation with each cytokine in various cell types. To know the role of JAK-STAT pathway in M1 differentiation, we have constructed dominant negative forms of STAT3 and established M1 cell lines that constitutively express them. These M1 cells that overexpressed dominant negative forms showed no induction of differentiation-associated markers including Fc gamma receptors, ferritin light chain, and lysozyme after …
引用总数
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