计算机辅助发现新型芳基烃受体配体,以调节炎症巨噬细胞中 CYP1A1 的表达。

IF 3.2 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Chemical Biology & Drug Design Pub Date : 2024-06-24 DOI:10.1111/cbdd.14572
Kerui Chen, Li Luo, Gao Tu, Jingyi Yang, Wang Pu, Junyu Zhu, Weiwei Xue, Rui Zhang
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引用次数: 0

摘要

环境因子芳基碳氢化合物受体(AhR)是连接外部环境信号(如环境内分泌干扰物 TCDD)和细胞内部过程的关键蛋白,参与激活外周巨噬细胞和人体的炎症反应。因此,通过靶向人AhR寻找抗巨噬细胞炎症反应的化合物受到广泛关注。在此,研究人员首先利用基于集合对接的虚拟筛选技术筛选了一个针对人AhR配体结合域(LBD)的化合物库(约20万个化合物),并确定了25个化合物作为潜在的抑制剂。然后,在这 25 种配体中发现有 9 种能下调 AhR 过度表达巨噬细胞中 CYP1A1(AhR 信号转导的下游基因)的 mRNA 表达。研究人员选择了最强效的化合物 AE-411/41415610 作进一步研究,发现它能降低小鼠腹腔巨噬细胞中 CYP1A1 的 mRNA 和蛋白表达水平。此外,蛋白芯片信号通路分析表明,AE-411/41415610在调控JAK-STAT和AKT-mTOR通路中发挥作用。总之,新发现的具有新支架的化合物为今后设计更有效的AhR靶向先导化合物以调节炎性腹腔巨噬细胞中CYP1A1的表达提供了一个起点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Computer-aided discovery of novel aryl hydrocarbon receptor ligands to regulate CYP1A1 expression in inflammatory macrophages

The environmental factor aryl hydrocarbon receptor (AhR), a key protein connecting the external environmental signals (e.g., environmental endocrine disruptor TCDD) to internal cellular processes, is involved in the activation of peripheral macrophages and inflammatory response in human body. Thus, there is widespread interest in finding compounds to anti-inflammatory response in macrophages by targeting human AhR. Here, ensemble docking based-virtual screening was first used to screen a library (~200,000 compounds) against human AhR ligand binding domain (LBD) and 25 compounds were identified as potential inhibitors. Then, 9 out of the 25 ligands were found to down-regulate the mRNA expression of CYP1A1 (a downstream gene of AhR signaling) in AhR overexpressing macrophages. The most potent compound AE-411/41415610 was selected for further study and found to reduce both mRNA and protein expressions level of CYP1A1 in mouse peritoneal macrophage. Moreover, protein chip signal pathway analysis indicated that AE-411/41415610 play a role in regulating JAK–STAT and AKT–mTOR pathways. In sum, the discovered hits with novel scaffolds provided a starting point for future design of more effective AhR-targeted lead compounds to regulate CYP1A1 expression of inflammatory peritoneal macrophages.

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来源期刊
Chemical Biology & Drug Design
Chemical Biology & Drug Design 医学-生化与分子生物学
CiteScore
5.10
自引率
3.30%
发文量
164
审稿时长
4.4 months
期刊介绍: Chemical Biology & Drug Design is a peer-reviewed scientific journal that is dedicated to the advancement of innovative science, technology and medicine with a focus on the multidisciplinary fields of chemical biology and drug design. It is the aim of Chemical Biology & Drug Design to capture significant research and drug discovery that highlights new concepts, insight and new findings within the scope of chemical biology and drug design.
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