Dispensability of Jak1 tyrosine kinase for interleukin-2-induced cell growth signaling in a human T cell line

被引:41
作者
Higuchi, M
Asao, H
Tanaka, N
Oda, K
Takeshita, T
Nakamura, M
VanSnick, J
Sugamura, K
机构
[1] TOHOKU UNIV,SCH MED,DEPT MICROBIOL,AOBA KU,SENDAI,MIYAGI 98077,JAPAN
[2] TOKYO MED & DENT UNIV,HUMAN GENE SCI CTR,TOKYO 113,JAPAN
[3] LUDWIG INST CANC RES,BRUSSELS BRANCH,BRUSSELS,BELGIUM
关键词
interleukin-2; receptor; Jak1; Jak3; Stat5;
D O I
10.1002/eji.1830260622
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The tyrosine kinases Jak1 and Jak3 are known to be associated with the beta and gamma chains of interleukin-2 receptor (IL-2R). They are activated by stimulation with IL-2, IL-4, IL-7, IL-9, or IL-15, receptors of which share the gamma chain of the IL-2R. We have obtained direct evidence of Jak1 association with the a chains of receptors for IL-4, IL-7 and IL-9 and with the beta chain of IL-2R, which is also common to the IL-15R. Furthermore, we have prepared mutant IL-2R beta chains with a mutation in the box 1 region, which is conserved among the IL-2R beta chain and the alpha chains of the other cytokine receptors sharing the IL-2R gamma chain. Using MOLT-4 transfectants with the mutant beta chains, we found that two conserved proline residues within the box 1 region are essentially involved in association with Jak1. The MOLT-4 transfectants with the mutant beta chains lacking Jak1 association showed IL-2 responsiveness, in terms of activation of Jak3 and Stat5 and induction of cell growth, indicating that Jak1 is dispensable for IL-2-mediated cell growth signaling and that Jak1 activation is not required for activation of Jak3 and Stat5 in the MOLT-4 transfectants.
引用
收藏
页码:1322 / 1327
页数:6
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