Identification of the human erythropoietin receptor region required for Stat1 and Stat3 activation

被引:59
作者
Kirito, K
Nakajima, K
Watanabe, T
Uchida, M
Tanaka, M
Ozawa, K
Komatsu, N [1 ]
机构
[1] Jichi Med Sch, Dept Med, Div Hematol, Minami Kawachi, Tochigi 3290498, Japan
[2] Osaka Univ, Sch Med, Biomed Res Ctr, Dept Mol Oncol, Suita, Osaka 565, Japan
关键词
D O I
10.1182/blood.V99.1.102
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Signal transducers and activators of transcription (Stat) proteins play important roles in the regulation of hematopoiesis as downstream molecules of cytokine signal transduction. It was previously demonstrated that erythropoietin (EPO), a major regulator of erythropoiesis, activates 3 different Stat members, Stat1, Stat3, and Stat5, in a human EPO-dependent cell line, UT-7/EPO. To clarity the mechanism by which EPO activates Stat1 and Stat3 via the EPO receptor (EPOR), a series of chimeric receptors was constructed bearing the extracellular domain of the granulocyte colony-stimulating factor receptor linked to the transmembrane domain of EPOR and the full length or several mutants of the cytoplasmic domain of EPOR, and these chimeric receptor complementary DNAs were introduced into UT-7/EPO cells. Tyr432 on human EPOR was important for activation of Stat1 and Stat3 and c-myc gene induction. In addition, Jak2 and Fes tyrosine kinases were Involved in EPO-induced activation of Stat1 and Stat3. These results indicate that Stat1 and Stat3 are activated by EPO via distinct mechanisms from Stat5.
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页码:102 / 110
页数:9
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