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

Authors :
Naama, Maria
Telpaz, Shahar
Awad, Aya
Ben-Simon, Shira
Harshuk-Shabso, Sarina
Modilevsky, Sonia
Rubin, Elad
Sawaed, Jasmin
Zelik, Lilach
Zigdon, Mor
Asulin, Nofar
Turjeman, Sondra
Werbner, Michal
Wongkuna, Supapit
Feeney, Rachel
Schröder, Björn O.
Nyska, Abraham
Nuriel-Ohayon, Meital
Bel, Shai
Naama, Maria
Telpaz, Shahar
Awad, Aya
Ben-Simon, Shira
Harshuk-Shabso, Sarina
Modilevsky, Sonia
Rubin, Elad
Sawaed, Jasmin
Zelik, Lilach
Zigdon, Mor
Asulin, Nofar
Turjeman, Sondra
Werbner, Michal
Wongkuna, Supapit
Feeney, Rachel
Schröder, Björn O.
Nyska, Abraham
Nuriel-Ohayon, Meital
Bel, Shai
Publication Year :
2023

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.<br />Appendix on pages e1–e4.

Details

Database :
OAIster
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1379028380
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1016.j.chom.2023.01.006