Janus kinases: components of multiple signaling pathways

被引:373
作者
Rane, SG [1 ]
Reddy, EP [1 ]
机构
[1] Temple Univ, Sch Med, Fels Inst Canc Res & Mol Biol, Philadelphia, PA 19140 USA
关键词
JAK kinases; STATs; ras; PI3K; CIS/JAB/SOCS/SIS protein family; signal transduction;
D O I
10.1038/sj.onc.1203925
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cytoplasmic Janus protein tyrosine kinases (JAKs) are crucial components of diverse signal transduction pathways that govern cellular survival, proliferation, differentiation and apoptosis, Evidence to date, indicates that JAK kinase function may integrate components of diverse signaling cascades, While it is likely that activation of STAT proteins may be an important function attributed to the JAK kinases, it is certainly not the only function performed by this key family of cytoplasmic tyrosine kinases, Emerging evidence indicates that phosphorylation of cytokine and growth factor receptors may be the primary functional attribute of JAK kinases. The JAK-triggered receptor phosphorylation can potentially be a rate-limiting event for a successful culmination of downstream signaling events. In support of this hypothesis, it has been found that JAK kinase function is required for optimal activation of the Src-kinase cascade, the Ras-MAP kinase pathway, the PI3K-AKT pathway and STAT signaling following the interaction of cytokine/interferon receptors with their ligands, Aberrations in JAK kinase activity, that may lead to derailment of one or more of the above mentioned pathways could disrupt normal cellular responses and result in disease states. Thus, over-activation of JAK kinases has been implicated in tumorigenesis, In contrast, loss of JAK kinase function has been found to result in disease states such as severe-combined immunodeficiency. In summary, optimal JAK kinase activity is a critical determinant of normal transmission of cytokine and growth factor signals.
引用
收藏
页码:5662 / 5679
页数:18
相关论文
共 213 条
  • [1] The Bcl-2 protein family: Arbiters of cell survival
    Adams, JM
    Cory, S
    [J]. SCIENCE, 1998, 281 (5381) : 1322 - 1326
  • [2] Granulocyte-macrophage colony-stimulating factor-activated signaling pathways in human neutrophils - Involvement of Jak2 in the stimulation of phosphatidylinositol 3-kinase
    Al-Shami, A
    Naccache, PH
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (09) : 5333 - 5338
  • [3] THE INTERLEUKIN-5/RECEPTOR INTERACTION ACTIVATES LYN AND JAK2 TYROSINE KINASES AND PROPAGATES SIGNALS VIA THE RAS-RAF-1-MAP KINASE AND THE JAK-STAT PATHWAYS IN EOSINOPHILS
    ALAM, R
    PAZDRAK, K
    STAFFORD, S
    FORSYTHE, P
    [J]. INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 1995, 107 (1-3) : 226 - 227
  • [4] The Bcl-2 protein family
    Antonsson, B
    Martinou, JC
    [J]. EXPERIMENTAL CELL RESEARCH, 2000, 256 (01) : 50 - 57
  • [5] IDENTIFICATION OF JAK2 AS A GROWTH-HORMONE RECEPTOR-ASSOCIATED TYROSINE KINASE
    ARGETSINGER, LS
    CAMPBELL, GS
    YANG, XN
    WITTHUHN, BA
    SILVENNOINEN, O
    IHLE, JN
    CARTERSU, C
    [J]. CELL, 1993, 74 (02) : 237 - 244
  • [6] INTERLEUKIN-3 SIGNALS THROUGH MULTIPLE ISOFORMS OF STAT5
    AZAM, M
    ERDJUMENTBROMAGE, H
    KREIDER, BL
    XIA, M
    QUELLE, F
    BASU, R
    SARIS, C
    TEMPST, P
    IHLE, JN
    SCHINDLER, C
    [J]. EMBO JOURNAL, 1995, 14 (07) : 1402 - 1411
  • [7] INTERLEUKIN-12 (IL-12) INDUCES TYROSINE PHOSPHORYLATION OF JAK2 AND TYK2 - DIFFERENTIAL USE OF JANUS FAMILY TYROSINE KINASES BY IL-2 AND IL-12
    BACON, CM
    MCVICAR, DW
    ORTALDO, JR
    REES, RC
    O'SHEA, JJ
    JOHNSTON, JA
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (01) : 399 - 404
  • [8] Bates ME, 1996, J IMMUNOL, V156, P711
  • [9] STRIPE-SPECIFIC REGULATION OF PAIR-RULE GENES BY HOPSCOTCH, A PUTATIVE JAK FAMILY TYROSINE KINASE IN DROSOPHILA
    BINARI, R
    PERRIMON, N
    [J]. GENES & DEVELOPMENT, 1994, 8 (03) : 300 - 312
  • [10] SHP1 protein tyrosine phosphatase negatively modulates erythroid differentiation and suppression of apoptosis in J2E erythroleukemic cells
    Bittorf, T
    Seiler, J
    Zhang, ZH
    Jaster, R
    Brock, J
    [J]. BIOLOGICAL CHEMISTRY, 1999, 380 (10) : 1201 - 1209