Interferon-induced guanylate-binding proteins in inflammasome activation and host defense

被引:115
|
作者
Kim, Bae-Hoon [1 ,2 ]
Chee, Jonathan D. [2 ]
Bradfield, Clinton J. [2 ]
Park, Eui-Soon [2 ]
Kumar, Pradeep [2 ]
MacMicking, John D. [1 ,2 ,3 ]
机构
[1] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Dept Microbial Pathogenesis, New Haven, CT USA
[3] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT USA
关键词
PATHOGEN-CONTAINING VACUOLES; IFN-INDUCIBLE GTPASES; NLRP3; INFLAMMASOME; CELL-DEATH; AIM2; INCREASES SUSCEPTIBILITY; MGBP2; CONTROLS; GAMMA; CASPASE-11; IMMUNITY;
D O I
10.1038/ni.3440
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Traditional views of the inflammasome highlight the assembly of pre-existing core components shortly after infection or tissue damage. Emerging work, however, suggests that the inflammasome machinery is also subject to 'tunable' or inducible signals that might accelerate its autocatalytic properties and dictate where inflammasome assembly takes place in the cell. Many of these signals operate downstream of interferon receptors to elicit inflammasome regulators, including a new family of interferon-induced GTPases called 'guanylate-binding proteins' (GBPs). Here we investigate the critical roles of interferon-induced GBPs in directing inflammasome subtype-specific responses and their consequences for cell-autonomous immunity to a wide variety of microbial pathogens. We discuss emerging mechanisms of action and the potential effect of these GBPs on predisposition to sepsis and other infectious or inflammatory diseases.
引用
收藏
页码:481 / U189
页数:9
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