Liu Youhua, Liu Jiaqi, Ren Ruiti, Xin Zimeng, Luo Yaojun, Chen Yushi, Huang Chaoqun, Liu Yuxi, Yang Tongyudan, Wang Xinxia
College of Animal Sciences, Zhejiang University, Hangzhou, Zhejiang, China.
Key Laboratory of Animal Nutrition and Feed Science (Eastern of China), Ministry of Agriculture and Rural Affairs, Hangzhou, China.
Microbiome. 2025 Mar 17;13(1):75. doi: 10.1186/s40168-025-02047-4.
Although short-term high-fat diet (S-HFD) and long-term high-fat diet (L-HFD) induce metabolic disorder, the underlying epigenetic mechanism is still unclear.
Here, we found that both 4 days of S-HFD and 10 weeks of L-HFD increased mRNA mA level in epididymal white adipose tissue (eWAT) and impaired metabolic health. Interestingly, S-HFD activated transposable elements (TEs), especially endogenous retroviruses (ERVs) in eWAT, while L-HFD activated long interspersed elements (LINEs). Subsequently, we demonstrated that both S-HFD and L-HFD increased mA level of Ehmt2 and decreased EHMT2 protein expression and H3K9me2 level, accounting for activation of ERVs and LINEs. Overexpression of EHMT2 in eWAT or inhibition of ERVs and LINEs by antiviral therapy improved metabolic health under HFD feeding. Notably, we found that both short-term and long-term HFD feeding increased Fimicutes/Bacteroidota ratio and decreased the gut microbiome health index. Fecal microbiota transplantation (FMT) experiments demonstrated that gut microbiota from S-HFD and L-HFD was responsible for increased mA level in eWAT, resulting in glucose intolerance and insulin insensitivity. Furthermore, we identified that both S-HFD and L-HFD increased the abundance of the gut microbial metabolite homogentisic acid (HGA), and HGA level was positively correlated with unclassified_f__Lachnospiraceae which was both increased in S-HFD and L-HFD feeding mice. Administration of HGA increased the mA level of Ehmt2 and decreased the EHMT2 protein expression and H3K9me2 level in eWAT, leading to metabolic disorder in mice.
Together, this study reveals a novel mechanism that S-HFD and L-HFD induce metabolism disorder through gut microbiota-HGA-mA-Ehmt2-ERV/LINE signaling. These findings may provide a novel insight for prevention and treatment of metabolism disorder upon short-term or long-term dietary fat intake. Video Abstract.
尽管短期高脂饮食(S-HFD)和长期高脂饮食(L-HFD)会诱发代谢紊乱,但其潜在的表观遗传机制仍不清楚。
在此,我们发现4天的S-HFD和10周的L-HFD均会增加附睾白色脂肪组织(eWAT)中的mRNA mA水平,并损害代谢健康。有趣的是,S-HFD激活了eWAT中的转座元件(TEs),尤其是内源性逆转录病毒(ERVs),而L-HFD激活了长散在元件(LINEs)。随后,我们证明S-HFD和L-HFD均会增加Ehmt2的mA水平,并降低EHMT2蛋白表达和H3K9me2水平,这解释了ERVs和LINEs的激活。在高脂饮食喂养下,在eWAT中过表达EHMT2或通过抗病毒疗法抑制ERVs和LINEs可改善代谢健康。值得注意的是,我们发现短期和长期高脂饮食喂养均会增加厚壁菌门/拟杆菌门的比例,并降低肠道微生物群健康指数。粪便微生物群移植(FMT)实验表明,来自S-HFD和L-HFD的肠道微生物群是导致eWAT中mA水平升高的原因,从而导致葡萄糖不耐受和胰岛素不敏感。此外,我们确定S-HFD和L-HFD均会增加肠道微生物代谢产物尿黑酸(HGA)的丰度,并且HGA水平与未分类的毛螺菌科呈正相关,在S-HFD和L-HFD喂养的小鼠中该菌科均增加。给予HGA会增加eWAT中Ehmt2的mA水平,并降低EHMT2蛋白表达和H3K9me2水平,导致小鼠出现代谢紊乱。
总之,本研究揭示了一种新机制,即S-HFD和L-HFD通过肠道微生物群-HGA-mA-Ehmt2-ERV/LINE信号传导诱导代谢紊乱。这些发现可能为短期或长期饮食脂肪摄入后代谢紊乱的预防和治疗提供新的见解。视频摘要。