Short-term and long-term high-fat diet promote metabolic disorder through reprogramming mRNA m6A in white adipose tissue by gut microbiota.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
Youhua Liu, Jiaqi Liu, Ruiti Ren, Zimeng Xin, Yaojun Luo, Yushi Chen, Chaoqun Huang, Yuxi Liu, Tongyudan Yang, Xinxia Wang
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引用次数: 0

Abstract

Background: 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.

Results: Here, we found that both 4 days of S-HFD and 10 weeks of L-HFD increased mRNA m6A 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 m6A 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 m6A 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 m6A level of Ehmt2 and decreased the EHMT2 protein expression and H3K9me2 level in eWAT, leading to metabolic disorder in mice.

Conclusions: Together, this study reveals a novel mechanism that S-HFD and L-HFD induce metabolism disorder through gut microbiota-HGA-m6A-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.

短期和长期高脂肪饮食通过肠道菌群对白色脂肪组织mRNA m6A的重编程促进代谢紊乱。
背景:虽然短期高脂肪饮食(S-HFD)和长期高脂肪饮食(L-HFD)诱导代谢紊乱,但其潜在的表观遗传机制尚不清楚。结果:在这里,我们发现4天的S-HFD和10周的L-HFD都增加了附睾白色脂肪组织(eWAT)的mRNA m6A水平,并损害了代谢健康。有趣的是,S-HFD激活了eWAT中的转座因子(TEs),特别是内源性逆转录病毒(ERVs),而L-HFD激活了长穿插因子(LINEs)。随后,我们证明了S-HFD和L-HFD都增加了Ehmt2的m6A水平,降低了Ehmt2蛋白表达和H3K9me2水平,这是erv和LINEs激活的原因。EHMT2在eWAT中的过表达或通过抗病毒治疗抑制ERVs和LINEs可改善HFD喂养下的代谢健康。值得注意的是,我们发现短期和长期喂食HFD都增加了有限菌门/拟杆菌门比例,降低了肠道微生物群健康指数。粪便微生物群移植(FMT)实验表明,S-HFD和L-HFD的肠道微生物群导致eWAT中m6A水平升高,导致葡萄糖耐受不良和胰岛素不敏感。此外,我们发现S-HFD和L-HFD均增加了肠道微生物代谢产物均质酸(HGA)的丰度,并且HGA水平与未分类的_f_ lachnospiraceae呈正相关,在S-HFD和L-HFD喂养的小鼠中均增加。HGA增加eWAT中Ehmt2的m6A水平,降低Ehmt2蛋白表达和H3K9me2水平,导致小鼠代谢紊乱。结论:本研究揭示了S-HFD和L-HFD通过肠道微生物群- hga - m6a - ehmt2 - erv /LINE信号诱导代谢紊乱的新机制。这些发现可能为预防和治疗短期或长期饮食脂肪摄入引起的代谢紊乱提供新的见解。视频摘要。
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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