上睑下垂
坏死性下垂
生物
程序性细胞死亡
免疫系统
先天免疫系统
模式识别受体
炎症体
细胞生物学
受体
信号转导
炎症
细胞凋亡
细胞因子
促炎细胞因子
免疫学
微生物学
遗传学
作者
David E. Place,SangJoon Lee,Thirumala‐Devi Kanneganti
标识
DOI:10.1016/j.mib.2020.07.012
摘要
The immune system has evolved multiple mechanisms to restrict microbial infections and regulate inflammatory responses. Without appropriate regulation, infection-induced inflammatory pathology can be deadly. The innate immune system recognizes the microbial molecules conserved in many pathogens and engages a rapid response by producing inflammatory mediators and activating programmed cell death pathways, including pyroptosis, apoptosis, and necroptosis. Activation of pattern recognition receptors, in combination with inflammatory cytokine-induced signaling through death domain-containing receptors, initiates a highly interconnected cell death process called PANoptosis (pyroptosis, apoptosis, necroptosis). Broadly speaking, PANoptosis is critical for restricting a wide range of pathogens (including bacteria, viruses, fungi, and parasites), which we describe in this review. We propose that re-examining the role of cell death and inflammatory cytokines through the lens of PANoptosis will advance our understanding of host–pathogen evolution and may reveal new treatment strategies for controlling a wide range of infectious diseases.
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