Wang Huirong, Peng Xingrong, Ge Yunjun, Zhang Shuo, Wang Zhenyi, Fan Yu, Huang Wei, Qiu Minghua, Ye Richard D
Institute of Chinese Medical Sciences, State Key Laboratory of Quality Research in Chinese Medicine, University of Macau, Macau, Macau.
Department of Biology, Southern University of Science and Technology, Shenzhen, China.
Front Pharmacol. 2020 Mar 24;11:337. doi: 10.3389/fphar.2020.00337. eCollection 2020.
Formyl peptide receptors (FPRs) are G protein-coupled receptors (GPCRs) widely expressed in neutrophils and other phagocytes. FPRs play important roles in host defense, inflammation, and the pathogenesis of infectious and inflammatory diseases. Because of these functions, FPRs are potential targets for anti-inflammatory therapies. In order to search for potentially novel anti-inflammatory agents, we examined (Lingzhi), a Chinese medicinal herbs known for its anti-inflammatory effects, and found that compound 18 (C18) derived from could limit the inflammatory response through FPR-related signaling pathways. Further studies showed that C18 could bind to FPR2 and induce conformation change of the receptor that differed from the conformational change induced by the pan-agonist, WKYMVm. C18 inhibited at the receptor level and blocked WKYMVm signaling through FPR2, resulting in reduced superoxide production and compromised cell chemotaxis. These results identified for the first time that a -derived component with inhibitory effects that acts through a G protein-coupled receptor FPR2. Considering its less than optimal IC value, further optimization of C18 would be necessary for future applications.
甲酰肽受体(FPRs)是一种G蛋白偶联受体(GPCRs),在中性粒细胞和其他吞噬细胞中广泛表达。FPRs在宿主防御、炎症以及感染性和炎症性疾病的发病机制中发挥着重要作用。由于这些功能,FPRs是抗炎治疗的潜在靶点。为了寻找潜在的新型抗炎药物,我们研究了具有抗炎作用的中药材(灵芝),发现从灵芝中提取的化合物18(C18)可通过FPR相关信号通路限制炎症反应。进一步研究表明,C18可与FPR2结合并诱导受体构象变化,这种变化不同于全激动剂WKYMVm诱导的构象变化。C18在受体水平发挥抑制作用,并通过FPR2阻断WKYMVm信号传导,从而减少超氧化物的产生并损害细胞趋化性。这些结果首次确定了一种通过G蛋白偶联受体FPR2发挥抑制作用的灵芝衍生成分。考虑到其IC值不太理想,未来应用中需要对C18进行进一步优化。