Therapeutic regulation of the NLRP3 inflammasome in chronic inflammatory diseases

被引:78
|
作者
Seok, Jin Kyung [1 ]
Kang, Han Chang [1 ]
Cho, Yong-Yeon [1 ]
Lee, Hye Suk [1 ]
Lee, Joo Young [1 ]
机构
[1] Catholic Univ Korea, Coll Pharm, BK21 PLUS Team, Bucheon 14662, South Korea
基金
新加坡国家研究基金会;
关键词
Innate immunity; Inflammation; Pattern recognition receptors; Drug development; Small molecule inhibitors; FATTY LIVER-DISEASE; PROPIONIBACTERIUM-ACNES; RHEUMATOID-ARTHRITIS; ATOPIC-DERMATITIS; AMYLOID-BETA; K+ EFFLUX; PHARMACOLOGICAL INHIBITOR; CASPASE-1; ACTIVATION; COGNITIVE IMPAIRMENT; PATTERN-RECOGNITION;
D O I
10.1007/s12272-021-01307-9
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Inflammasomes are cytosolic pattern recognition receptors that recognize pathogen-associated molecular patterns (PAMPs) and danger-associated molecular patterns (DAMPs) derived from invading pathogens and damaged tissues, respectively. Upon activation, the inflammasome forms a complex containing a receptor protein, an adaptor, and an effector to induce the autocleavage and activation of procaspase-1 ultimately culminating in the maturation and secretion of IL-1 beta and IL-18 and pyroptosis. Inflammasome activation plays an important role in host immune responses to pathogen infections and tissue repair in response to cellular damage. The NLRP3 inflammasome is a well-characterized pattern recognition receptor and is well known for its critical role in the regulation of immunity and the development and progression of various inflammatory diseases. In this review, we summarize recent efforts to develop therapeutic applications targeting the NLRP3 inflammasome to cure and prevent chronic inflammatory diseases. This review extensively discusses NLRP3 inflammasome-related diseases and current development of small molecule inhibitors providing beneficial information on the design of therapeutic strategies for NLRP3 inflammasome-related diseases. Additionally, small molecule inhibitors are classified depending on direct or indirect targeting mechanism to describe the current status of the development of pharmacological inhibitors.
引用
收藏
页码:16 / 35
页数:20
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