天然产物
炎症体
炎症
细胞生物学
化学
医学
免疫学
生物
生物化学
作者
Emily McMahon,Sherihan El‐Sayed,Jack Green,Christopher Hoyle,Lorna M. FitzPatrick,Emma V. Jones,Eve Corrie,Rebecca L. Kelly,Mairi Challinor,Sally Freeman,Richard A. Bryce,Catherine B. Lawrence,David Brough,Paul R. Kasher
出处
期刊:iScience
[Cell Press]
日期:2024-02-01
卷期号:27 (2): 108968-108968
标识
DOI:10.1016/j.isci.2024.108968
摘要
Excessive or aberrant NLRP3 inflammasome activation has been implicated in the progression and initiation of many inflammatory conditions; however, currently no NLRP3 inflammasome inhibitors have been approved for therapeutic use in the clinic. Here we have identified that the natural product brazilin effectively inhibits both priming and activation of the NLRP3 inflammasome in cultured murine macrophages, a human iPSC microglial cell line and in a mouse model of acute peritoneal inflammation. Through computational modeling, we predict that brazilin can adopt a favorable binding pose within a site of the NLRP3 protein which is essential for its conformational activation. Our results not only encourage further evaluation of brazilin as a therapeutic agent for NLRP3-related inflammatory diseases, but also introduce this small-molecule as a promising scaffold structure for the development of derivative NLRP3 inhibitor compounds.
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