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肠道微生物群对固有屏障防御的翻译调控。

Translational control of innate barrier defense by the gut microbiota.

作者信息

Li Yun, Wu Runrun, Ma Xianda, Zhang Jianglin, Ma Junjie, Duan Yiran, Hassell Brian, Ruhn Kelly A, Behrendt Cassie L, Dende Chaitanya, Wang Li, Lemoff Andrew, Raj Prithvi, Kuang Zheng, Hooper Lora V

机构信息

Department of Immunology, University of Texas Southwestern Medical Center, Dallas, TX 75390.

Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA 15213.

出版信息

bioRxiv. 2025 Aug 11:2025.08.11.668728. doi: 10.1101/2025.08.11.668728.

Abstract

The intestinal epithelium is protected by a mucus barrier, infused with antimicrobial proteins, that restricts microbial access to host tissue. Because assembling this barrier is energetically costly, its production must be tightly regulated. Here, we show that the microbiota regulates the translation of key mucus barrier components, including the structural glycoprotein mucin 2 and the antimicrobial enzyme lysozyme. This process is initiated by microbial induction of histone deacetylase 5 (HDAC5) in secretory epithelial cells of the intestine. HDAC5 promotes deacetylation of 14-3-3 proteins, enabling activation of the energy sensing kinase mTOR which enhances translation of mucus and antimicrobial proteins. These findings reveal a mechanism by which the microbiota controls barrier immunity at the level of protein synthesis and suggest that the HDAC5-mTOR axis integrates microbial and energetic signals to regulate intestinal defense.

摘要

肠道上皮受到一层充满抗菌蛋白的黏液屏障保护,该屏障限制微生物接触宿主组织。由于组装这一屏障的能量消耗巨大,其产生必须受到严格调控。在此,我们表明微生物群调节关键黏液屏障成分的翻译,包括结构糖蛋白黏蛋白2和抗菌酶溶菌酶。这一过程由肠道分泌上皮细胞中微生物诱导组蛋白脱乙酰酶5(HDAC5)启动。HDAC5促进14-3-3蛋白的去乙酰化,从而激活能量感应激酶mTOR,增强黏液和抗菌蛋白的翻译。这些发现揭示了一种微生物群在蛋白质合成水平控制屏障免疫的机制,并表明HDAC5-mTOR轴整合微生物和能量信号以调节肠道防御。

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