粘液
分泌物
生物
自噬
杯状细胞
细胞生物学
炎症
未折叠蛋白反应
某种肠道细菌
囊性纤维化
内质网
微生物学
免疫学
肠道菌群
内分泌学
上皮
生物化学
遗传学
细胞凋亡
生态学
作者
Maria Naama,Shahar Telpaz,Aya Awad,Shira Ben-Simon,Sarina Harshuk-Shabso,Sonia Modilevsky,Elad Rubin,Jasmin Sawaed,Lilach Zelik,Mor Zigdon,Nofar Asulin,Sondra Turjeman,Michal Werbner,Supapit Wongkuna,R Feeney,Bjoern O. Schroeder,Abraham Nyska,Meital Nuriel‐Ohayon,Shai Bel
标识
DOI:10.1016/j.chom.2023.01.006
摘要
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.
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