PIAS1 selectively inhibits interferon-inducible genes and is important in innate immunity

被引:210
作者
Liu, B
Mink, S
Wong, KA
Stein, N
Getman, C
Dempsey, PW
Wu, H
Shuai, K [1 ]
机构
[1] Univ Calif Los Angeles, Dept Med, Div Hematol Oncol, Los Angeles, CA 90024 USA
[2] Univ Calif Los Angeles, Dept Biol Chem, Los Angeles, CA 90024 USA
[3] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90024 USA
[4] Univ Calif Los Angeles, Dept Mol & Med Pharmacol, Los Angeles, CA 90024 USA
[5] Univ Calif Los Angeles, Howard Hughes Med Inst, Los Angeles, CA 90024 USA
[6] Univ Calif Los Angeles, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90024 USA
关键词
D O I
10.1038/ni1104
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interferon (IFN) activates the signal transducer and activator of transcription (STAT) pathway to regulate immune responses. The protein inhibitor of activated STAT (PIAS) family has been suggested to negatively regulate STAT signaling. To understand the physiological function of PIAS1, we generated Pias1(-/-) mice. Using PIAS1-deficient cells, we show that PIAS1 selectively regulates a subset of IFN-gamma- or IFN-beta-inducible genes by interfering with the recruitment of STAT1 to the gene promoter. The antiviral activity of IFN-gamma or IFN-beta was consistently enhanced by Pias1 disruption. Pias1(-/-) mice showed increased protection against pathogenic infection. Our data indicate that PIAS1 is a physiologically important negative regulator of STAT1 and CL m suggest that PIAS1 is critical for the IFN-gamma- or IFN-beta-mediated innate immune responses.
引用
收藏
页码:891 / 898
页数:8
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