TYROSINE PHOSPHORYLATION AND ACTIVATION OF STAT5, STAT3, AND JANUS KINASES BY INTERLEUKIN-2 AND INTERLEUKIN-15

被引:322
作者
JOHNSTON, JA
BACON, CM
FINBLOOM, DS
REES, RC
KAPLAN, D
SHIBUYA, K
ORTALDO, JR
GUPTA, S
CHEN, YQ
GIRI, JD
OSHEA, JJ
机构
[1] US FDA,CTR BIOL EVALUAT & RES,DIV CYTOKINE BIOL,BETHESDA,MD 20892
[2] NCI,FREDERICK CANC RES & DEV CTR,DIV CANC TREATMENT,BIOL RESPONSE MODIFIERS PROGRAM,FREDERICK,MD 21702
[3] NCI,FREDERICK CANC RES & DEV CTR,ADV BIOSCI LABS,FREDERICK,MD 21702
[4] IMMUNEX RES & DEV CORP,SEATTLE,WA 98101
[5] COLUMBIA UNIV COLL PHYS & SURG,DEPT MED,NEW YORK,NY 10032
[6] UNIV SHEFFIELD,SCH MED,INST CANC STUDIES,SHEFFIELD S10 2RX,S YORKSHIRE,ENGLAND
关键词
D O I
10.1073/pnas.92.19.8705
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The cytokines interleukin 2 (IL-2) and IL-15 have similar biological effects on T cells and bind common hematopoietin receptor subunits. Pathways that involve Janus kinases (JAKs) and signal transducers and activators of transcription (STATs) have been shown to be important for hematopoietin receptor signaling. In this study we identify the STAT proteins activated by IL-2 and IL-15 in human T cells. IL-2 and IL-15 rapidly induced the tyrosine phosphorylation of STAT3 and STAT5, and DNA-binding complexes containing STAT3 and STAT5 were rapidly activated by these cytokines in T cells. IL 4 induced tyrosine phosphorylation and activation of STAT3 but not STATS. JAK1 and JAK3 were tyrosine-phosphorylated in response to IL-2 and IL-15. Hence, the JAK and STAT molecules that are activated in response to IL-2 and IL-15 are similar but differ from those induced by IL-4. These observations identify the STAT proteins activated by IL-2 and IL-15 and therefore define signaling pathways by which these T-cell growth factors may regulate gene transcription.
引用
收藏
页码:8705 / 8709
页数:5
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