Janus kinases and their role in growth and disease

被引:58
作者
Aringer, M [1 ]
Cheng, A [1 ]
Nelson, JW [1 ]
Chen, M [1 ]
Sudarshan, C [1 ]
Zhou, YJ [1 ]
O'Shea, JJ [1 ]
机构
[1] NIAMSD, Lymphocyte Biol Sect, Arthrit & Rheumatism Branch,Howard Hughes Med Ins, NIH,Natl Inst Hlth Res Scholars Program, Bethesda, MD 20892 USA
关键词
interferons; interleukins; cytokine receptors; signal transduction; Janus kinases;
D O I
10.1016/S0024-3205(98)00538-4
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Janus kinases (JAK) play a crucial role in the initial steps of cytokine signaling. Each of the four members (JAK1, JAK2, JAK3, TYK2) of this non-receptor tyrosine kinase family is indispensable for the effects of distinct cytokines. Moreover, recent reports have added to our knowledge on their highly specific functions: JAK3 knockout mice and JAK3 deficient patients cannot signal through the interleukin-2,4,7,9, or 15 receptors and suffer from severe combined immunodeficiency (SCID). JAK1 and JAK2 knockout mice do not survive, their cells again showing distinct patterns of cytokine signaling deficits. At the other end of the spectrum, JAK fusion proteins have been shown to play a role in leukemias. In addition, a new class of JAK-specific inhibitors was described by several groups, the CIS/SOCS/Jab family. This review on the rapidly growing field focuses on JAK function and regulation, and on their emerging role in development and human disease.
引用
收藏
页码:2173 / 2186
页数:14
相关论文
共 110 条
[71]   Jak2 is essential for signaling through a variety of cytokine receptors [J].
Parganas, E ;
Wang, D ;
Stravopodis, D ;
Topham, DJ ;
Marine, JC ;
Teglund, S ;
Vanin, EF ;
Bodner, S ;
Colamonici, OR ;
van Deursen, JM ;
Grosveld, G ;
Ihle, JN .
CELL, 1998, 93 (03) :385-395
[72]   Developmental defects of lymphoid cells in Jak3 kinase-deficient mice [J].
Park, SY ;
Saijo, K ;
Takahashi, T ;
Osawa, M ;
Arase, H ;
Hirayama, N ;
Miyake, K ;
Nakauchi, H ;
Shirasawa, T ;
Saito, T .
IMMUNITY, 1995, 3 (06) :771-782
[73]   Fusion of TEL, the ETS-variant gene 6 (ETV6), to the receptor-associated kinase JAK2 as a result of t(9;12) in a lymphoid and t(9;15;12) in a myeloid leukemia [J].
Peeters, P ;
Raynaud, SD ;
Cools, J ;
Wlodarska, I ;
Grosgeorge, J ;
Philip, P ;
Monpoux, F ;
VanRompaey, L ;
Baens, M ;
VandenBerghe, H ;
Marynen, P .
BLOOD, 1997, 90 (07) :2535-2540
[74]   2 MEMBERS OF THE JAK FAMILY OF PROTEIN TYROSINE KINASES MAP TO CHROMOSOME-1P31.3 AND CHROMOSOME-9P24 [J].
PRITCHARD, MA ;
BAKER, E ;
CALLEN, DF ;
SUTHERLAND, GR ;
WILKS, AF .
MAMMALIAN GENOME, 1992, 3 (01) :36-38
[75]   THE INTERLEUKIN-2 RECEPTOR GAMMA-CHAIN MAPS TO XQ13.1 AND IS MUTATED IN X-LINKED SEVERE COMBINED IMMUNODEFICIENCY, SCIDX1 [J].
PUCK, JM ;
DESCHENES, SM ;
PORTER, JC ;
DUTRA, AS ;
BROWN, CJ ;
WILLARD, HF ;
HENTHORN, PS .
HUMAN MOLECULAR GENETICS, 1993, 2 (08) :1099-1104
[76]   Genomic sequence, organization, and chromosomal localization of human JAK3 [J].
Riedy, MC ;
Dutra, AS ;
Blake, TB ;
Modi, W ;
Lal, BK ;
Davis, J ;
Bosse, A ;
OShea, JJ ;
Johnston, JA .
GENOMICS, 1996, 37 (01) :57-61
[77]   Disruption of the Jak1 gene demonstrates obligatory and nonredundant roles of the jaks in cytokine-lnduced biologic responses [J].
Rodig, SJ ;
Meraz, MA ;
White, JM ;
Lampe, PA ;
Riley, JK ;
Arthur, CD ;
King, KL ;
Sheehan, KCF ;
Yin, L ;
Pennica, D ;
Johnson, EM ;
Schreiber, RD .
CELL, 1998, 93 (03) :373-383
[78]   IL4 and IL13 receptors share the gamma c chain and activate STAT6, STAT3 and STAT5 proteins in normal human B cells [J].
Rolling, C ;
Treton, D ;
Pellegrini, S ;
Galanaud, P ;
Richard, Y .
FEBS LETTERS, 1996, 393 (01) :53-56
[79]   MUTATION OF JAK3 IN A PATIENT WITH SCID - ESSENTIAL ROLE OF JAK3 IN LYMPHOID DEVELOPMENT [J].
RUSSELL, SM ;
TAYEBI, N ;
NAKAJIMA, H ;
RIEDY, MC ;
ROBERTS, JL ;
AMAN, MJ ;
MIGONE, TS ;
NOGUCHI, M ;
MARKERT, ML ;
BUCKLEY, RH ;
O'SHEA, JJ ;
LEONARD, WJ .
SCIENCE, 1995, 270 (5237) :797-800
[80]   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