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