Regulation of cytokine receptor signaling by SOCS1

被引:55
作者
Ilangumaran, S
Rottapel, R
机构
[1] Princess Margaret Hosp, Univ Hlth Network, Ontario Canc Inst, Toronto, ON M5G 2M9, Canada
[2] Univ Toronto, Dept Med, Toronto, ON, Canada
[3] Univ Toronto, Dept Immunol, Toronto, ON, Canada
[4] Univ Toronto, Dept Med Biophys, Toronto, ON, Canada
[5] St Michaels Hosp, Toronto, ON M5B 1W8, Canada
关键词
D O I
10.1034/j.1600-065X.2003.00020.x
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 suppressor of cytokine signaling (SOCS) family of proteins is a novel class of negative feedback regulators of cytokine receptor signaling. SOCS1 is rapidly induced following stimulation by several type I and type II cytokines, and it attenuates their signaling by its ability to bind and inhibit all four of the Janus family of intracellular tyrosine kinases (JAKs). Studies from our own and other laboratories have documented another important function of SOCS1 in facilitating ubiquitination of protein substrates and their subsequent proteasomal degradation. SOCS1 also functions as a potential tumor suppressor by inhibiting several hematopoietic oncogenes. In addition to these negative regulatory functions, we have recently shown a positive regulatory role for SOCS1 in increasing the stability of major histocompatibility complex (MHC) class II proteins by preventing their degradation. These findings illustrate multiple roles for SOCS1 in cytokine receptor signaling, and provide groundwork for detailed analysis of the role of SOCS1 in pre-T cell receptor (TCR) and TCR signaling, and regulation of T helper (Th)1 and Th2 differentiation.
引用
收藏
页码:196 / 211
页数:16
相关论文
共 107 条
[1]   Involvement of NH2-terminal sequences in the negative regulation of Vav signaling and transforming activity [J].
Abe, R ;
Whitehead, IP ;
O'Bryan, JP ;
Der, CJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (43) :30410-30418
[2]   Structural basis for relief of autoinhibition of the Dbl homology domain of proto-oncogene Vav by tyrosine phosphorylation [J].
Aghazadeh, B ;
Lowry, WE ;
Huang, XY ;
Rosen, MK .
CELL, 2000, 102 (05) :625-633
[3]   Suppressors of cytokine signalling (SOCS) in the immune system [J].
Alexander, WS .
NATURE REVIEWS IMMUNOLOGY, 2002, 2 (06) :410-416
[4]   SOCS1 is a critical inhibitor of interferon γ signaling and prevents the potentially fatal neonatal actions of this cytokine [J].
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 .
CELL, 1999, 98 (05) :597-608
[5]  
BAIRD PN, 1996, CURR OPIN IMMUNOL, V11, P157
[6]   Neutralization of interferon-γ in neonatal SOCS1-/- mice prevents fatty degeneration of the liver but not subsequent fatal inflammatory disease [J].
Bullen, DVR ;
Darwiche, R ;
Metcalf, D ;
Handman, E ;
Alexander, WS .
IMMUNOLOGY, 2001, 104 (01) :92-98
[7]   Regulatory and signaling properties of the Vav family [J].
Bustelo, XR .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (05) :1461-1477
[8]   Pim serine/threonine kinases regulate the stability of Socs-1 protein [J].
Chen, XP ;
Losman, JA ;
Cowan, S ;
Donahue, E ;
Fay, S ;
Vuong, BQ ;
Nawijn, MC ;
Capece, D ;
Cohan, VL ;
Rothman, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (04) :2175-2180
[9]   JAK-STAT signaling activated by Abl oncogenes [J].
Danial, NN ;
Rothman, P .
ONCOGENE, 2000, 19 (21) :2523-2531
[10]   Direct interaction of jak1 and v-Abl is required for v-Abl-induced activation of STATs and proliferation [J].
Danial, NN ;
Losman, JA ;
Lu, TH ;
Yip, N ;
Krishnan, K ;
Krolewski, J ;
Goff, SP ;
Wang, JYJ ;
Rothman, PB .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (11) :6795-6804