上睑下垂
褪黑素
脂肪组织
炎症体
脂肪细胞
促炎细胞因子
细胞生物学
化学
半胱氨酸蛋白酶1
生物
炎症
免疫学
内分泌学
作者
Lei Zhu,Lu Gan,Xu Yatao,Dan Luo,Qian Ren,Song Wu,Chao Sun
摘要
Abstract Pyroptosis is a proinflammatory form of cell death that is associated with pathogenesis of many chronic inflammatory diseases. Melatonin is substantially reported to possess anti‐inflammatory properties by inhibiting inflammasome activation. However, the effects of melatonin on inflammasome‐induced pyroptosis in adipocytes remain elusive. Here, we demonstrated that melatonin alleviated lipopolysaccharides ( LPS )‐induced inflammation and NLRP 3 inflammasome formation in mice adipose tissue. The NLRP 3 inflammasome‐mediated pyroptosis was also inhibited by melatonin in adipocytes. Further analysis revealed that gasdermin D ( GSDMD ), the key executioner of pyroptosis, was the target for melatonin inhibition of adipocyte pyroptosis. Importantly, we determined that nuclear factor κB ( NF ‐κB) signal was required for the GSDMD ‐mediated pyroptosis in adipocytes. We also confirmed that melatonin alleviated adipocyte pyroptosis by transcriptional suppression of GSDMD . Moreover, GSDMD physically interacted with interferon regulatory factor 7 ( IRF 7) and subsequently formed a complex to promote adipocyte pyroptosis. Melatonin also attenuated NLRP 3 inflammasome activation and pyroptosis, which was induced by LPS or obesity. In summary, our results demonstrate that melatonin alleviates inflammasome‐induced pyroptosis by blocking NF ‐κB/ GSDMD signal in mice adipose tissue. Our data reveal a novel function of melatonin on adipocyte pyroptosis, suggesting a new potential therapy for melatonin to prevent and treat obesity caused systemic inflammatory response.
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