吡喃结构域
目标2
炎症体
信号转导衔接蛋白
NALP3
细胞生物学
生物
先天免疫系统
NLRP1
免疫系统
TLR2型
炎症
上睑下垂
效应器
病毒学
细胞凋亡
免疫学
信号转导
半胱氨酸蛋白酶
程序性细胞死亡
遗传学
作者
Shruti Khare,Rojo A. Ratsimandresy,Lúcia de Almeida,Carla M. Cuda,Stephanie L. Rellick,Alexander V. Misharin,Melissa Wallin,Anu Gangopadhyay,Eleonora Forte,Eva Gottwein,Harris Perlman,John C. Reed,David R. Greaves,Andrea Dorfleutner,Christian Stehlik
摘要
The innate immune system responds to infection and tissue damage by activating cytosolic sensory complexes called 'inflammasomes'. Cytosolic DNA is sensed by AIM2-like receptors (ALRs) during bacterial and viral infections and in autoimmune diseases. Subsequently, recruitment of the inflammasome adaptor ASC links ALRs to the activation of caspase-1. A controlled immune response is crucial for maintaining homeostasis, but the regulation of ALR inflammasomes is poorly understood. Here we identified the PYRIN domain (PYD)-only protein POP3, which competes with ASC for recruitment to ALRs, as an inhibitor of DNA virus-induced activation of ALR inflammasomes in vivo. Data obtained with a mouse model with macrophage-specific POP3 expression emphasize the importance of the regulation of ALR inflammasomes in monocytes and macrophages.
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