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自噬通过缓解内质网应激控制肠道杯状细胞的黏液分泌。

Autophagy controls mucus secretion from intestinal goblet cells by alleviating ER stress.

机构信息

Azrieli Faculty of Medicine, Bar-Ilan University, Safed, Israel.

Department of Molecular Biology, Umeå University, Umeå, Sweden; Laboratory for Molecular Infection Medicine Sweden (MIMS), Umeå, Sweden.

出版信息

Cell Host Microbe. 2023 Mar 8;31(3):433-446.e4. doi: 10.1016/j.chom.2023.01.006. Epub 2023 Feb 3.

Abstract

Colonic goblet cells are specialized epithelial cells that secrete mucus to physically separate the host and its microbiota, thus preventing bacterial invasion and inflammation. How goblet cells control the amount of mucus they secrete is unclear. We found that constitutive activation of autophagy in mice via Beclin 1 enables the production of a thicker and less penetrable mucus layer by reducing endoplasmic reticulum (ER) stress. Accordingly, genetically inhibiting Beclin 1-induced autophagy impairs mucus secretion, while pharmacologically alleviating ER stress results in excessive mucus production. This ER-stress-mediated regulation of mucus secretion is microbiota dependent and requires the Crohn's-disease-risk gene Nod2. Overproduction of mucus alters the gut microbiome, specifically expanding mucus-utilizing bacteria, such as Akkermansia muciniphila, and protects against chemical and microbial-driven intestinal inflammation. Thus, ER stress is a cell-intrinsic switch that limits mucus secretion, whereas autophagy maintains intestinal homeostasis by relieving ER stress.

摘要

结肠杯状细胞是一种特殊的上皮细胞,它分泌黏液使宿主与其微生物群物理分离,从而防止细菌入侵和炎症。目前尚不清楚杯状细胞如何控制其分泌的黏液量。我们发现,通过 Beclin 1 使小鼠中的自噬持续激活,可以通过减少内质网 (ER) 应激来产生更厚且不易渗透的黏液层。因此,遗传抑制 Beclin 1 诱导的自噬会损害黏液分泌,而药理学缓解 ER 应激会导致过度的黏液产生。这种 ER 应激介导的黏液分泌的调节依赖于微生物群,并且需要克罗恩病风险基因 Nod2。黏液的过度产生会改变肠道微生物组,特别是会扩张利用黏液的细菌,如 Akkermansia muciniphila,并能预防化学物质和微生物驱动的肠道炎症。因此,ER 应激是一种细胞内开关,限制黏液分泌,而自噬通过缓解 ER 应激来维持肠道内稳态。

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