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
相关论文
共 36 条
[21]   ACTIVATION OF JAK2 KINASE MEDIATED BY THE INTERLEUKIN-6 SIGNAL TRANSDUCER GP130 [J].
NARAZAKI, M ;
WITTHUHN, BA ;
YOSHIDA, K ;
SILVENNOINEN, O ;
YASUKAWA, K ;
IHLE, JN ;
KISHIMOTO, T ;
TAGA, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (06) :2285-2289
[22]   INTERLEUKIN-2 INDUCES TYROSINE PHOSPHORYLATION AND NUCLEAR TRANSLOCATION OF STAT3 IN HUMAN T-LYMPHOCYTES [J].
NIELSEN, M ;
SVEJGAARD, A ;
SKOV, S ;
ODUM, N .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (12) :3082-3086
[23]   MULTISTEP REGULATION OF ENHANCER ACTIVITY OF THE 21-BASE-PAIR ELEMENT OF HUMAN T-CELL LEUKEMIA-VIRUS TYPE-I [J].
NIKI, M ;
OHTANI, K ;
NAKAMURA, M ;
SUGAMURA, K .
JOURNAL OF VIROLOGY, 1992, 66 (07) :4348-4357
[24]   JAK2 ASSOCIATES WITH THE BETA(C) CHAIN OF THE RECEPTOR FAR GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR, AND ITS ACTIVATION REQUIRES THE MEMBRANE-PROXIMAL REGION [J].
QUELLE, FW ;
SATO, N ;
WITTHUHN, BS ;
INHORN, RC ;
EDER, M ;
MIYAJIMA, A ;
GRIFFIN, JD ;
IHLE, JN .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (07) :4335-4341
[25]  
REAULD JC, 1992, P NATL ACAD SCI USA, V89, P5690
[26]   13 HYBRIDOMAS SECRETING HAPTEN-SPECIFIC IMMUNOGLOBULIN-E FROM MICE WITH IGA OR IGB HEAVY-CHAIN HAPLOTYPE [J].
RUDOLPH, AK ;
BURROWS, PD ;
WABL, MR .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1981, 11 (06) :527-529
[27]   INTERACTION OF IL-2R-BETA AND GAMMA(C) CHAINS WITH JAK1 AND JAK3 - IMPLICATIONS FOR XSCID AND XCID [J].
RUSSELL, SM ;
JOHNSTON, JA ;
NOGUCHI, M ;
KAWAMURA, M ;
BACON, CM ;
FRIEDMANN, M ;
BERG, M ;
MCVICAR, DW ;
WITTHUHN, BA ;
SILVENNOINEN, O ;
GOLDMAN, AS ;
SCHMALSTIEG, FC ;
IHLE, JN ;
OSHEA, JJ ;
LEONARD, WJ .
SCIENCE, 1994, 266 (5187) :1042-1045
[28]   THE COMMON GAMMA-CHAIN FOR MULTIPLE CYTOKINE RECEPTORS [J].
SUGAMURA, K ;
ASAO, H ;
KONDO, M ;
TANAKA, N ;
ISHII, N ;
NAKAMURA, M ;
TAKESHITA, T .
ADVANCES IN IMMUNOLOGY, VOL 59, 1995, 59 :225-277
[29]  
Suzuki J, 1989, Int Immunol, V1, P373, DOI 10.1093/intimm/1.4.373
[30]   MONOCLONAL-ANTIBODY DEFINING A MOLECULE POSSIBLY IDENTICAL TO THE P75 SUBUNIT OF INTERLEUKIN-2 RECEPTOR [J].
TAKESHITA, T ;
GOTO, Y ;
TADA, K ;
NAGATA, K ;
ASAO, H ;
SUGAMURA, K .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 169 (04) :1323-1332