Gut microbiota and metabolite interface-mediated hepatic inflammation.

Immunometabolism (Cobham (Surrey, England)) Pub Date : 2024-01-25 eCollection Date: 2024-01-01 DOI:10.1097/IN9.0000000000000037
Ming Yang, Katina Massad, Eric T Kimchi, Kevin F Staveley-O'Carroll, Guangfu Li
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Abstract

Immunologic and metabolic signals regulated by gut microbiota and relevant metabolites mediate bidirectional interaction between the gut and liver. Gut microbiota dysbiosis, due to diet, lifestyle, bile acids, and genetic and environmental factors, can advance the progression of chronic liver disease. Commensal gut bacteria have both pro- and anti-inflammatory effects depending on their species and relative abundance in the intestine. Components and metabolites derived from gut microbiota-diet interaction can regulate hepatic innate and adaptive immune cells, as well as liver parenchymal cells, significantly impacting liver inflammation. In this mini review, recent findings of specific bacterial species and metabolites with functions in regulating liver inflammation are first reviewed. In addition, socioeconomic and environmental factors, hormones, and genetics that shape the profile of gut microbiota and microbial metabolites and components with the function of priming or dampening liver inflammation are discussed. Finally, current clinical trials evaluating the factors that manipulate gut microbiota to treat liver inflammation and chronic liver disease are reviewed. Overall, the discussion of microbial and metabolic mediators contributing to liver inflammation will help direct our future studies on liver disease.

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肠道微生物群与代谢物界面介导的肝脏炎症
由肠道微生物群和相关代谢物调节的免疫和代谢信号介导了肠道和肝脏之间的双向互动。由于饮食、生活方式、胆汁酸以及遗传和环境因素造成的肠道微生物群失调,会推进慢性肝病的发展。肠道共生细菌具有促炎和抗炎作用,这取决于它们在肠道中的种类和相对丰度。肠道微生物群与饮食相互作用产生的成分和代谢物可调节肝脏先天性和适应性免疫细胞以及肝实质细胞,从而对肝脏炎症产生重大影响。在这篇微型综述中,首先回顾了最近发现的具有调节肝脏炎症功能的特定细菌种类和代谢物。此外,还讨论了社会经济和环境因素、激素和遗传等影响肠道微生物群特征的因素,以及具有引发或抑制肝脏炎症功能的微生物代谢物和成分。最后,还回顾了目前评估操纵肠道微生物群因素以治疗肝脏炎症和慢性肝病的临床试验。总之,对导致肝脏炎症的微生物和代谢介质的讨论将有助于指导我们未来对肝病的研究。
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