褪黑激素通过MTNR1B调节METTL3,保护回肠细胞分化。

IF 4.5 2区 医学 Q2 CELL BIOLOGY
Inflammation Pub Date : 2025-04-01 Epub Date: 2024-07-17 DOI:10.1007/s10753-024-02098-z
Yuanyuan Li, Yan Sun, Yaoxing Chen, Yulan Dong
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引用次数: 0

摘要

肠道干细胞能迅速分化成各种上皮细胞,在维持肠道平衡方面发挥着至关重要的作用。褪黑素是一种已知的内源性分子,具有抗炎和抗氧化特性,但其在回肠干细胞分化中的潜在功效至今尚未完全清楚。这项研究表明,褪黑激素能抑制回肠炎症,并通过MTNR1B维持回肠干细胞的正常分化。使用MTNR1B抑制剂治疗后的后续结果进一步证实了这些发现。此外,METTL3蛋白的过度表达似乎是促进回肠炎症和细胞分化紊乱的潜在诱因。用METTL3抑制剂SAH治疗可明显抑制回肠炎症和Wnt/β-catenin活性,从而维持正常的细胞分化功能。总之,本研究表明,褪黑素可通过MTNR1B抑制METTL3的异常表达,从而改善回肠炎症并维持细胞分化功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Melatonin via MTNR1B regulates METTL3 to protect ileum cell differentiation.

Melatonin via MTNR1B regulates METTL3 to protect ileum cell differentiation.

Intestinal stem cells rapidly differentiate into various epithelial cells, playing a crucial role in maintaining intestinal homeostasis. Melatonin, a known endogenous molecule with anti-inflammatory and antioxidant properties, has its potential efficacy in ileum stem cells differentiation not fully understood to date. This study indicates that melatonin suppresses ileum inflammation and maintains normal differentiation of ileum stem cells through MTNR1B. Subsequent outcomes following treatment with MTNR1B inhibitors further substantiate these findings. Additionally, overexpression of METTL3 protein appears to be a potential instigator for promoting ileum inflammation and disruptions in cell differentiation. Treatment with the METTL3 inhibitor SAH significantly inhibits ileum inflammation and Wnt/β-catenin activity, thereby sustaining normal cellular differentiation functions. In summary, this study showed that melatonin may improve ileum inflammation and maintain cell differentiation functions by inhibiting abnormal METTL3 expression via MTNR1B.

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来源期刊
Inflammation
Inflammation 医学-免疫学
CiteScore
9.70
自引率
0.00%
发文量
168
审稿时长
3.0 months
期刊介绍: Inflammation publishes the latest international advances in experimental and clinical research on the physiology, biochemistry, cell biology, and pharmacology of inflammation. Contributions include full-length scientific reports, short definitive articles, and papers from meetings and symposia proceedings. The journal''s coverage includes acute and chronic inflammation; mediators of inflammation; mechanisms of tissue injury and cytotoxicity; pharmacology of inflammation; and clinical studies of inflammation and its modification.
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