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肝细胞 TM4SF5 表达与非酒精性脂肪性肝病发展过程中肠道微生物群失调的关系。

Association between hepatocyte TM4SF5 expression and gut microbiome dysbiosis during non-alcoholic fatty liver disease development.

机构信息

Department of Pharmacy, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.

Department of Pharmacy, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea; Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.

出版信息

Life Sci. 2024 Dec 1;358:123164. doi: 10.1016/j.lfs.2024.123164. Epub 2024 Oct 23.

Abstract

Gut microbiome dysbiosis is involved in non-alcoholic fatty liver disease (NAFLD) development. Hepatic transmembrane 4 L six family member 5 (TM4SF5) overexpression promotes NAFLD. However, how gut microbiota are associated with TM4SF5-mediated NAFLD remains unexplored. We analyzed the gut microbiome using feces from hepatocyte-specific TM4SF5-overexpressing transgenic (Alb-TG, TG) or Tm4sf5 knock-out (KO) mice fed a normal chow diet (NCD), high-fat diet (HFD) for 2 weeks (HFD), or methionine-choline-deficient diet (MCD) for 4 weeks to investigate associations among Tm4sf5 expression, diet, and the gut microbiome. TG-NCD mice showed a higher Firmicutes-to-Bacteroidetes (F/B) ratio, with less enrichment of Akkermansia muciniphila and Lactobacillus reuteri. NASH-related microbiomes in feces were more abundant in TG-HFD mice than in KO-HFD mice. Further, TG-MCD showed a higher F/B ratio than TG-NCD or KO mice, with decreases or increases in microbiomes beneficial or detrimental to the liver, respectively. Such effects in TG-MCD animals were correlated with functional pathways producing short-chain fatty acids (SCFAs). Furthermore, potential functional pathways of the gut microbiome were metabolically parallel to NAFLD features in TG-MCD mice. These results suggest that hepatocyte Tm4sf5 supports gut microbiome dysbiosis and metabolic activity, leading to SCFA production and hepatic inflammation during NAFLD development.

摘要

肠道微生物群落失调与非酒精性脂肪性肝病(NAFLD)的发展有关。肝跨膜 4 L 六家族成员 5(TM4SF5)的过表达促进了 NAFLD 的发生。然而,肠道微生物群如何与 TM4SF5 介导的 NAFLD 相关仍不清楚。我们使用肝细胞特异性 TM4SF5 过表达转基因(Alb-TG,TG)或 Tm4sf5 敲除(KO)小鼠的粪便分析了肠道微生物组,这些小鼠分别用正常饲料(NCD)、高脂肪饮食(HFD)喂养 2 周(HFD)或蛋氨酸-胆碱缺乏饮食(MCD)喂养 4 周。研究 Tm4sf5 表达、饮食和肠道微生物群之间的关联。TG-NCD 小鼠表现出更高的厚壁菌门与拟杆菌门(F/B)比值,阿克曼氏菌属和罗伊氏乳杆菌的丰度降低。与 KO-HFD 小鼠相比,TG-HFD 小鼠粪便中存在更多的 NASH 相关微生物组。此外,与 TG-NCD 或 KO 小鼠相比,TG-MCD 显示出更高的 F/B 比值,分别导致对肝脏有益或有害的微生物组减少或增加。TG-MCD 动物的这些影响与产生短链脂肪酸(SCFAs)的功能途径相关。此外,肠道微生物组的潜在功能途径在代谢上与 TG-MCD 小鼠的 NAFLD 特征平行。这些结果表明,肝细胞 Tm4sf5 支持肠道微生物群落失调和代谢活性,导致 SCFA 产生和 NAFLD 发展过程中的肝炎症。

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