Interferon-induced guanylate-binding proteins: Guardians of host defense in health and disease

被引:187
|
作者
Tretina, Kyle [1 ,2 ,3 ,4 ]
Park, Eui-Soon [1 ,2 ,3 ,4 ]
Maminska, Agnieszka [1 ,2 ,3 ,4 ]
MacMicking, John D. [1 ,2 ,3 ,4 ]
机构
[1] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
[2] Yale Syst Biol Inst, West Haven, CT 06516 USA
[3] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06520 USA
[4] Yale Univ, Sch Med, Dept Microbial Pathogenesis, New Haven, CT 06520 USA
来源
JOURNAL OF EXPERIMENTAL MEDICINE | 2019年 / 216卷 / 03期
基金
美国国家卫生研究院;
关键词
PATHOGEN-CONTAINING VACUOLES; SINGLE-CELL TRANSCRIPTOMICS; IFN-INDUCIBLE GTPASES; GAMMA-INTERFERON; NUCLEOTIDE-BINDING; AUTOPHAGY PROTEINS; AIM2; INFLAMMASOME; ALPHA-INTERFERON; GENE-EXPRESSION; MGBP2; CONTROLS;
D O I
10.1084/jem.20182031
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Guanylate-binding proteins (GBPs) have recently emerged as central orchestrators of immunity to infection, inflammation, and neoplastic diseases. Within numerous host cell types, these IFN-induced GTPases assemble into large nanomachines that execute distinct host defense activities against a wide variety of microbial pathogens. In addition, GBPs customize inflammasome responses to bacterial infection and sepsis, where they act as critical rheostats to amplify innate immunity and regulate tissue damage. Similar functions are becoming evident for metabolic inflammatory syndromes and cancer, further underscoring the importance of GBPs within infectious as well as altered homeostatic settings. A better understanding of the basic biology of these IFN-induced GTPases could thus benefit clinical approaches to a wide spectrum of important human diseases.
引用
收藏
页码:482 / 500
页数:19
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