Negative regulation of cytokine signaling pathways

被引:512
作者
Yasukawa, H [1 ]
Sasaki, A [1 ]
Yoshimura, A [1 ]
机构
[1] Kurume Univ, Inst Life Sci, Kurume, Fukuoka 8390861, Japan
关键词
JAK; STAT; CIS; JAB; SOCS; SSI; SH2; domain; tyrosine kinase; negative regulation; interferon gamma;
D O I
10.1146/annurev.immunol.18.1.143
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 Janus family of protein tyrosine kinases (JAKs) and STAT transcription factors regulate cellular processes involved in cell growth, differentiation, and transformation through their association with cytokine receptors. The CIS family of proteins (also referred to as the SOCS or SSI family) has been implicated in the regulation of signal transduction by a variety of cytokines. Most of them appear to be induced after stimulation with several different cytokines, and at least three of them (CIS1, CIS3/SOCS-3, and JAB/SOCS1) negatively regulate cytokine signal transduction by various means: CIS 1 inhibits STAT5 activation by binding to cytokine receptors that recruit STAT5, whereas JAB/SOCS-1 and CIS3/SOCS-3 directly bind to the kinase domain of JAKs, thereby inhibiting tyrosine-kinase activity. Therefore, these CIS family members seem to function in a classical negative feedback loop of cytokine signaling. Biochemical characterization as well as gene disruption studies indicate that JAB/SOCS1/SSI-1 is an important negative regulator of interferon gamma signaling. The mechanisms by which these inhibitors of cytokine signal transduction exert their effects have been extensively studied and will provide useful information for regulating tyrosine-kinase activity.
引用
收藏
页码:143 / 164
页数:22
相关论文
共 101 条
  • [1] SOCS1 is a critical inhibitor of interferon γ signaling and prevents the potentially fatal neonatal actions of this cytokine
    Alexander, WS
    Starr, R
    Fenner, JE
    Scott, GL
    Handman, E
    Sprigg, NS
    Corbin, JE
    Cornish, AL
    Darwiche, R
    Owczarek, CM
    Kay, TWH
    Nicola, NA
    Hertzog, PJ
    Metcalf, D
    Hilton, DJ
    [J]. CELL, 1999, 98 (05) : 597 - 608
  • [2] Autoregulation of pituitary corticotroph SOCS-3 expression: Characterization of the murine SOCS-3 promoter
    Auernhammer, CJ
    Bousquet, C
    Melmed, S
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (12) : 6964 - 6969
  • [3] Pituitary corticotroph SOCS-3: Novel intracellular regulation of leukemia-inhibitory factor-mediated proopiomelanocortin gene expression and adrenocorticotropin secretion
    Auernhammer, CJ
    Chesnokova, V
    Bousquet, C
    Melmed, S
    [J]. MOLECULAR ENDOCRINOLOGY, 1998, 12 (07) : 954 - 961
  • [4] Functionally distinct isoforms of STAT5 are generated by protein processing
    Azam, M
    Lee, C
    Strehlow, I
    Schindler, C
    [J]. IMMUNITY, 1997, 6 (06) : 691 - 701
  • [5] Erythropoietin and interleukin-3 activate tyrosine phosphorylation of CBL and association with CRK adaptor proteins
    Barber, DL
    Mason, JM
    Fukazawa, T
    Reedquist, KA
    Druker, BJ
    Band, H
    DAndrea, AD
    [J]. BLOOD, 1997, 89 (09) : 3166 - 3174
  • [6] Identification of SOCS-3 as a potential mediator of central leptin resistance
    Bjorbaek, C
    Elmquist, JK
    Frantz, JD
    Shoelson, SE
    Flier, JS
    [J]. MOLECULAR CELL, 1998, 1 (04) : 619 - 625
  • [7] BOWTELL DDL, 1995, ONCOGENE, V11, P1561
  • [8] Stat3 activation is required for cellular transformation by v-src
    Bromberg, JF
    Horvath, CM
    Besser, D
    Lathem, WW
    Darnell, JE
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (05) : 2553 - 2558
  • [9] Interleukin-10 (IL-10) selectively enhances CIS3/SOCS3 mRNA expression in human neutrophils: Evidence for an IL-10-induced pathway that is independent of STAT protein activation
    Cassatella, MA
    Gasperini, S
    Bovolenta, C
    Calzetti, F
    Vollebregt, M
    Scapini, P
    Marchi, M
    Suzuki, R
    Suzuki, A
    Yoshimura, A
    [J]. BLOOD, 1999, 94 (08) : 2880 - 2889
  • [10] Crystal structure of a tyrosine phosphorylated STAT-1 dimer bound to DNA
    Chen, XM
    Vinkemeier, U
    Zhao, YX
    Jeruzalmi, D
    Darnell, JE
    Kuriyan, J
    [J]. CELL, 1998, 93 (05) : 827 - 839