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人脱落乳牙来源的干细胞缓解肝硬化解毒素 D 执行的肝细胞焦亡抑制

Stem Cells From Human Exfoliated Deciduous Teeth Alleviate Liver Cirrhosis Inhibition of Gasdermin D-Executed Hepatocyte Pyroptosis.

机构信息

Department of Orthodontics, Peking University School and Hospital of Stomatology, Beijing, China.

National Clinical Research Center for Oral Diseases and National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing, China.

出版信息

Front Immunol. 2022 May 12;13:860225. doi: 10.3389/fimmu.2022.860225. eCollection 2022.

Abstract

Liver cirrhosis represents a type of end-stage liver disease with few effective therapies, which was characterized by damaged functional liver tissue due to long-term inflammation. Gasdermin D (GSDMD)-executed programmed necrosis is reported to be involved in inflammation. However, the role of GSDMD in liver cirrhosis remains unclear. In this study, we used a CCl-induced cirrhosis model and found stem cells from human exfoliated deciduous teeth (SHED) infusion showed profound therapeutic effects for liver cirrhosis. Mechanistically, NLRP3 inflammasome-activated GSDMD and its pyroptosis were upregulated in liver cirrhosis, while SHED infusion could suppress the expression of GSDMD and Caspase-1, resulting in reduced hepatocyte pyroptosis and inflammatory cytokine IL-1β release. Consistently, SHED could inhibit the elevated expression of NLRP3, GSDMD and Caspase-1 induced by CCl treatment co-culture system, which was mediated by decreasing reactive oxygen species (ROS) generation. Moreover, the pyroptosis inhibitor disulfiram showed similar therapeutic effects for liver cirrhosis as SHED. In conclusion, SHED alleviates CCl-induced liver cirrhosis inhibition of hepatocytes pyroptosis. Our findings could provide a potential treatment strategy and novel target for liver cirrhosis.

摘要

肝硬化是一种终末期肝病,治疗方法有限,其特征是由于长期炎症导致功能性肝组织受损。Gasdermin D (GSDMD)-执行的程序性细胞坏死被报道与炎症有关。然而,GSDMD 在肝硬化中的作用尚不清楚。在本研究中,我们使用 CCl4 诱导的肝硬化模型发现,人脱落乳牙来源的干细胞(SHED)输注对肝硬化有显著的治疗作用。在机制上,NLRP3 炎性小体激活的 GSDMD 及其细胞焦亡在肝硬化中上调,而 SHED 输注可以抑制 GSDMD 和 Caspase-1 的表达,导致肝实质细胞焦亡和炎症细胞因子 IL-1β 的释放减少。一致地,SHED 可以抑制 CCl4 处理的共培养系统中 NLRP3、GSDMD 和 Caspase-1 的上调,这是通过减少活性氧(ROS)的产生介导的。此外,细胞焦亡抑制剂双硫仑对肝硬化的治疗效果与 SHED 相似。总之,SHED 减轻了 CCl4 诱导的肝硬化,抑制了肝实质细胞的细胞焦亡。我们的研究结果为肝硬化提供了一种潜在的治疗策略和新的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2e0/9133376/928efce06923/fimmu-13-860225-g001.jpg

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