A distinct function of STAT proteins in erythropoietin signal transduction

被引:60
作者
Kirito, K [1 ]
Uchida, M [1 ]
Yamada, M [1 ]
Miura, Y [1 ]
Komatsu, N [1 ]
机构
[1] JICHI MED SCH,DEPT MED,DIV HEMATOL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
关键词
D O I
10.1074/jbc.272.26.16507
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 Janus kinase (JAK)-signal transducers and activators of transcription (STAT) pathway is an important signaling pathway of interferons and cytokines. We examined the activation of STAT proteins induced by interleukin-3 (IL-3), granulocyte-macrophage colony-stimulating factor (GM CSP), or erythropoietin (EPO) using the human leukemia cell line, UT-7, which requires these cytokines for growth. IL-3, GM-CSF, and EPO induced DNA-binding activity to the oligonucleotides corresponding to the sis-inducible elements (SIE) of c-fos, in addition to the beta-casein promoter (beta-CAP), SIE- and beta-CAP-binding proteins were identical to Stat1 alpha and Stat3 complex and to Stat5 protein, respectively. This indicates that IL-3, GM CSF, and EPO commonly activated Stat1 alpha, Stat3, and Stat5 proteins in UT-7. However, EPO hardly activated Stat1 alpha and Stat3 in UT-7/GM, which is a subline of UT-7 that grows slightly in response to EPO. Transfection studies revealed that UT7/GM cells constitutively expressing Stat1 alpha, but not Stat3, can grow as well in response to EPO as GM-CSF, suggesting that Stat1 alpha is involved in the EPO-induced proliferation of UT-7. Thus, although Stat1 alpha, Stat3, and Stat5 proteins are activated by GM-CSF, IL-3, and EPO, our data suggest that each STAT protein has a distinctive role in the actions of cytokines.
引用
收藏
页码:16507 / 16513
页数:7
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