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NLRP3 炎性小体小分子抑制剂的特性及其在急性肺损伤中的潜在应用。

Characterization of a small molecule inhibitor of the NLRP3 inflammasome and its potential use for acute lung injury.

机构信息

Department of Medicinal Chemistry, Virginia Commonwealth University, Richmond, VA 23298, USA.

Department of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA 23298, USA.

出版信息

Bioorg Chem. 2024 Sep;150:107562. doi: 10.1016/j.bioorg.2024.107562. Epub 2024 Jun 17.

Abstract

Accumulating data support the key roles of the NLRP3 inflammasome, an essential component of the innate immune system, in human pathophysiology. As an emerging drug target and a potential biomarker for human diseases, small molecule inhibitors of the NLRP3 inflammasome have been actively pursued. Our recent studies identified a small molecule, MS-II-124, as a potent NLRP3 inhibitor and potential imaging probe. In this report, MS-II-124 was further characterized by an unbiased and comprehensive analysis through Eurofins BioMAP Diversity PLUS panel that contains 12 human primary cell-based systems. The analysis revealed promising activities of MS-II-124 on inflammation and immune functions, further supporting the roles of the NLRP3 inflammasome in these model systems. Further studies of MS-II-124 in mouse model of acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) and NLRP3 knockout mice demonstrated its target engagement, efficacy to suppress inflammatory cytokines and infiltration of immune cells in the lung tissues. In summary, the results support the therapeutic potential of MS-II-124 as a NLRP3 inhibitor and warrant future studies of this compound and its analogs to develop therapeutics for ALI/ARDS.

摘要

越来越多的数据支持 NLRP3 炎性小体作为先天免疫系统的重要组成部分,在人类病理生理学中的关键作用。作为一个新兴的药物靶点和人类疾病的潜在生物标志物,NLRP3 炎性小体的小分子抑制剂已被积极研究。我们最近的研究发现了一种小分子 MS-II-124,它是一种有效的 NLRP3 抑制剂和潜在的成像探针。在本报告中,通过包含 12 个人源原代细胞系的 Eurofins BioMAP Diversity PLUS 面板进行了全面的、无偏见的分析,进一步对 MS-II-124 进行了表征。分析显示 MS-II-124 在炎症和免疫功能方面具有有前景的活性,进一步支持 NLRP3 炎性小体在这些模型系统中的作用。进一步在急性肺损伤 (ALI)/急性呼吸窘迫综合征 (ARDS) 小鼠模型和 NLRP3 敲除小鼠中研究 MS-II-124,表明其可结合靶点,能有效抑制肺部炎症细胞因子的释放和免疫细胞浸润。总之,这些结果支持 MS-II-124 作为 NLRP3 抑制剂的治疗潜力,并为该化合物及其类似物的进一步研究提供了依据,以开发用于 ALI/ARDS 的治疗药物。

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