WSX-1 and glycoprotein 130 constitute a signal-transducing receptor for IL-27

被引:570
作者
Pflanz, S [1 ]
Hibbert, L [1 ]
Mattson, J [1 ]
Rosales, R [1 ]
Vaisberg, E [1 ]
Bazan, JF [1 ]
Phillips, JH [1 ]
McClanahan, TK [1 ]
Malefyt, RD [1 ]
Kastelein, RA [1 ]
机构
[1] DNA Res Inst, Palo Alto, CA 94304 USA
关键词
D O I
10.4049/jimmunol.172.4.2225
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 recently discovered cytokine IL-27 belongs to the IL-6/IL-12 family of cytokines and induced proliferation of naive CD4(+) T cells and the generation of a Th1-type adaptive immune response. Although binding of IL-27 to the cytokine receptor WSX-1 was demonstrated, this interaction proved insufficient to mediate cellular effects. Hence, IL-27 was believed to form a heteromeric signaling receptor complex with WSX-1 and another, yet to be identified, cytokine receptor subunit. In this study, we describe that WSX-1 together with gp130 constitutes a functional signal-transducing receptor for IL-27. We show that neither of the two subunits itself is sufficient to mediate IL-27-induced signal transduction, but that the combination of both is required for this event. Expression analysis of WSX-1 and gp130 by quantitative PCR suggests that IL-27 might have a variety of cellular targets besides naive CD4(+) T cells: we demonstrate gene induction of a subset of inflammatory cytokines in primary human mast cells and monocytes in response to IL-27 stimulation. Thus, IL-27 not only contributes to the development of an adaptive immune response through its action on CD4(+) T cells, it also directly acts on cells of the innate immune system.
引用
收藏
页码:2225 / 2231
页数:7
相关论文
共 26 条
[1]   Postnatally induced inactivation of gp130 in mice results in neurological, cardiac, hematopoietic, immunological, hepatic, and pulmonary defects [J].
Betz, UAK ;
Bloch, W ;
van den Broek, M ;
Yoshida, K ;
Taga, T ;
Kishimoto, T ;
Addicks, K ;
Rajewsky, K ;
Müller, W .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (10) :1955-1965
[2]  
Bolin LM, 1997, J NEUROSCI, V17, P5493
[3]   Novel IL-12 family members shed light on the orchestration of Th1 responses [J].
Brombacher, F ;
Kastelein, RA ;
Alber, G .
TRENDS IN IMMUNOLOGY, 2003, 24 (04) :207-212
[4]  
Chang JT, 2000, EUR J IMMUNOL, V30, P1113, DOI 10.1002/(SICI)1521-4141(200004)30:4<1113::AID-IMMU1113>3.0.CO
[5]  
2-P
[6]   Development of Th1-type immune responses requires the type I cytokine receptor TCCR [J].
Chen, Q ;
Ghilardi, N ;
Wang, H ;
Baker, T ;
Xie, MH ;
Gurney, A ;
Grewal, IS ;
de Sauvage, FJ .
NATURE, 2000, 407 (6806) :916-920
[7]   STRUCTURAL-ANALYSIS OF THE HUMAN INTERFERON-GAMMA RECEPTOR - A SMALL SEGMENT OF THE INTRACELLULAR DOMAIN IS SPECIFICALLY REQUIRED FOR CLASS-I MAJOR HISTOCOMPATIBILITY COMPLEX ANTIGEN INDUCTION AND ANTIVIRAL ACTIVITY [J].
COOK, JR ;
JUNG, V ;
SCHWARTZ, B ;
WANG, PY ;
PESTKA, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (23) :11317-11321
[8]   Molecular mechanisms of cytokine receptor activation [J].
Grötzinger, J .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2002, 1592 (03) :215-223
[9]   Leukocystatin, a new class II cystatin expressed selectively by hematopoietic cells [J].
Halfon, S ;
Ford, J ;
Foster, J ;
Dowling, L ;
Lucian, L ;
Sterling, M ;
Xu, YM ;
Weiss, M ;
Ikeda, M ;
Liggett, D ;
Helms, A ;
Caux, C ;
Lebecque, S ;
Hannum, C ;
Menon, S ;
McClanahan, T ;
Gorman, D ;
Zurawski, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (26) :16400-16408
[10]   Interleukin-6-type cytokine signalling through the gp130/Jak/STAT pathway [J].
Heinrich, PC ;
Behrmann, I ;
Müller-Newen, G ;
Schaper, F ;
Graeve, L .
BIOCHEMICAL JOURNAL, 1998, 334 :297-314