Cross-regulation of JAK and Src kinases

被引:42
作者
Ingley, E
Klinken, SP
机构
[1] Western Australian Inst Med Res, Lab Can Med, Perth, WA 6000, Australia
[2] Univ Western Australia, Med Res Ctr, Perth, WA 6009, Australia
关键词
Janus kinase; Src kinase; cytokine receptor; Lyn; erythropoietin;
D O I
10.1080/08977190500368031
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Members of the Janus kinase (JAK) family, JAK1, JAK2, JAK3 and Tyk2 are intimately involved in the signalling events initiated by cytokines activating cell surface receptors. They are responsible for phosphorylating these receptors, which create docking sites for downstream molecules such as the signal transducer and activator of transcription family members. In addition, cytokine receptors associate with members of the Src family kinase (SFK). JAKs and SFK work in concert to activate many of the signalling molecules, with both kinase families required for optimal transmission of intracellular signals. JAKs and SFK are also required for the activation and recruitment of negative regulators of cytokine signalling, e.g., protein tyrosine phosphatases (PTPs) and suppressors of cytokine signalling. Aberrant activity of the JAK-Src kinase duet can result in hemopoietic abnormalities including leukaemia. Additionally, the recent identification of a somatic JAK2 mutation as the cause of polycythema vera, further highlights the clinical importance of these molecules.
引用
收藏
页码:89 / 95
页数:7
相关论文
共 72 条
  • [1] 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
  • [2] Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
    Baxter, EJ
    Scott, LM
    Campbell, PJ
    East, C
    Fourouclas, N
    Swanton, S
    Vassiliou, GS
    Bench, AJ
    Boyd, EM
    Curtin, N
    Scott, MA
    Erber, WN
    Green, AR
    [J]. LANCET, 2005, 365 (9464) : 1054 - 1061
  • [3] Stat3-mediated Myc expression is required for Src transformation and PDGF-induced mitogenesis
    Bowman, T
    Broome, MA
    Sinibaldi, D
    Wharton, W
    Pledger, WJ
    Sedivy, JM
    Irby, R
    Yeatman, T
    Courtneidge, SA
    Jove, R
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (13) : 7319 - 7324
  • [4] Phosphoprotein associated with glycosphingolipid-enriched microdomains (PAG), a novel ubiquitously expressed transmembrane adaptor protein, binds the protein tyrosine kinase Csk and is involved in regulation of T cell activation
    Brdicka, T
    Pavilstová, D
    Leo, A
    Bruyns, E
    Korínek, V
    Angelisová, P
    Scherer, J
    Shevchenko, A
    Shevchenko, A
    Hilgert, I
    Cerny, J
    Drbal, K
    Kuramitsu, Y
    Kornacker, B
    Horejsí, V
    Schraven, B
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (09) : 1591 - 1604
  • [5] Cao XM, 1996, MOL CELL BIOL, V16, P1595
  • [6] Constitutive activation of Stat3 signaling confers resistance to apoptosis in human U266 myeloma cells
    Catlett-Falcone, R
    Landowski, TH
    Oshiro, MM
    Turkson, J
    Levitzki, A
    Savino, R
    Ciliberto, G
    Moscinski, L
    Fernández-Luna, JL
    Nuñez, G
    Dalton, WS
    Jove, R
    [J]. IMMUNITY, 1999, 10 (01) : 105 - 115
  • [7] Catlett-Falcone Robyn, 1999, Current Opinion in Oncology, V11, P490, DOI 10.1097/00001622-199911000-00010
  • [8] Src kinases and not JAKs activate STATs during IL-3 induced myeloid cell proliferation
    Chaturvedi, P
    Reddy, MVR
    Reddy, EP
    [J]. ONCOGENE, 1998, 16 (13) : 1749 - 1758
  • [9] Abrogation of interleukin-3 dependence of myeloid cells by the v-src oncogene requires SH2 and SH3 domains which specify activation of STATs
    Chaturvedi, P
    Sharma, S
    Reddy, EP
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (06) : 3295 - 3304
  • [10] Chin H, 1998, BLOOD, V91, P3734