Mitochondrial reactive zones in antiviral innate immunity

被引:10
|
作者
Yasukawa, Kai [1 ]
Koshiba, Takumi [2 ]
机构
[1] Kyushu Univ, Fac Sci, Dept Biol, Fukuoka 8190395, Japan
[2] Fukuoka Univ, Fac Sci, Dept Chem, Fukuoka 8140180, Japan
来源
关键词
Innate immunity; MAVS; Mitochondria; NLRP3; inflammasomes; RLR pathway; RNA virus; RIG-I; SIGNALING PROTEIN; NLRP3; INFLAMMASOME; DNA; HOST; MAVS; INDUCTION; RESPONSES; DISEASE; NLRX1;
D O I
10.1016/j.bbagen.2020.129839
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondria are multi-functioning organelles that participate in a wide range of biologic processes from energy metabolism to cellular suicide. Mitochondria are also involved in the cellular innate immune response against microorganisms or environmental irritants, particularly in mammals. Mitochondrial-mediated innate immunity is achieved by the activation of two discrete signaling pathways, the NLR family pyrin domain-containing 3 inflammasomes and the retinoic acid-inducible gene I-like receptor pathway. In both pathways, a mitochondrial outer membrane adaptor protein, called mitochondrial antiviral signaling MAVS, and mitochondria-derived components play a key role in signal transduction. In this review, we discuss current insights regarding the fundamental phenomena of mitochondrial-related innate immune responses, and review the specific roles of various mitochondrial subcompartments in fine-tuning innate immune signaling events. We propose that specific targeting of mitochondrial functions is a potential therapeutic approach for the management of infectious diseases and autoinflammatory disorders with an excessive immune response.
引用
收藏
页数:8
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