Differential inhibition of IL-6-type cytokine-induced STAT activation by PMA

被引:5
作者
Terstegen, L
Maassen, BG
Radtke, S
Behrmann, I
Schaper, F
Heinrich, PC
Graeve, L
Gatsios, P
机构
[1] Rhein Westfal TH Aachen, Inst Biochem, D-55057 Aachen, Germany
[2] Rhein Westfal TH Aachen, Interdisziplinares Zentrum Klin Forsch, D-52074 Aachen, Germany
关键词
cytokine signaling; cross-talk; mitogen-activated protein kinase; signal transducer and activator of transcription; suppressor of cytokine signaling;
D O I
10.1016/S0014-5793(00)01826-3
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
Prior activation of mitogen-activated protein kinases br phorbol 13-myristate 12-acetate (PMA) results in an inhibition of interleukin (IL)-6-induced activation of the Janus kinase/signal transducer and activator of transcription (STAT) signaling pathway which is most likely mediated by the induction of suppressor of cytokine signaling-3 and requires the specific SHP2 binding site Y759 of the IL-6 signal transducer gp130. In this study, we demonstrate that PMA inhibits STAT activation by IL-6 and the related cytokine leukemia inhibitory factor (LIF) hut not by oncostatin M (OSM). Since the LIF receptor also contains an SHP2 recruitment site whereas the OSM receptor lacks such a module, we propose that two SHP2 binding modules within a homo- or heterodimeric receptor are necessary to mediate the PMA inhibitory effect. (C) 2000 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:100 / 104
页数:5
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