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褪黑素调控 LPS 诱导的结肠炎症中 N6-腺苷甲基化(m6A)的作用机制。

The Effect Mechanism of N6-adenosine Methylation (m6A) in Melatonin Regulated LPS-induced Colon Inflammation.

机构信息

Laboratory of Neurobiology, College of Veterinary Medicine, China Agricultural University, Beijing, People's Republic of China.

Key Laboratory of Precision Nutrition and Food Quality, Ministry of Education, Department of Nutrition and Health, China Agricultural University, Beijing, People's Republic of China.

出版信息

Int J Biol Sci. 2024 Apr 15;20(7):2491-2506. doi: 10.7150/ijbs.95316. eCollection 2024.

Abstract

Colon inflammation is characterized by disturbances in the intestinal microbiota and inflammation. Melatonin (Mel) can improve colon inflammation. However, the underlying mechanism remains unclear. Recent studies suggest that m6A methylation modification may play an important role in inflammatory responses. This study aimed to explore the effects of melatonin and LPS-mediated m6A methylation on colon inflammation. Our study found that melatonin inhibits M1 macrophages, activates M2 macrophages, inhibit the secretion of pro-inflammatory factors, maintain colon homeostasis and improves colon inflammation through MTNR1B. In addition, the increased methylation level of m6A is associated with the occurrence of colon inflammation, and melatonin can also reduce the level of colon methylation to improve colon inflammation. Among them, the main methylated protein METTL3 can be inhibited by melatonin through MTNR1B. In a word, melatonin regulates m6A methylation by improving abnormal METTL3 protein level to reshape the microflora and activate macrophages to improve colon inflammation, mainly through MTNR1B.

摘要

结肠炎症的特征是肠道微生物群和炎症的紊乱。褪黑素(Mel)可以改善结肠炎。然而,其潜在机制尚不清楚。最近的研究表明,m6A 甲基化修饰可能在炎症反应中发挥重要作用。本研究旨在探讨褪黑素和 LPS 介导的 m6A 甲基化对结肠炎症的影响。我们的研究发现,褪黑素通过 MTNR1B 抑制 M1 巨噬细胞,激活 M2 巨噬细胞,抑制促炎因子的分泌,维持结肠内稳态并改善结肠炎症。此外,m6A 甲基化水平的升高与结肠炎症的发生有关,褪黑素还可以降低结肠的甲基化水平,从而改善结肠炎症。其中,主要的甲基化蛋白 METTL3 可以通过 MTNR1B 被褪黑素抑制。总之,褪黑素通过改善异常的 METTL3 蛋白水平来调节 m6A 甲基化,重塑微生物群并激活巨噬细胞,从而改善结肠炎症,主要通过 MTNR1B 实现。

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