Foxo1 controls gut homeostasis and commensalism by regulating mucus secretion

Author:

Chen Zuojia12ORCID,Luo Jialie2ORCID,Li Jian2ORCID,Kim Girak2ORCID,Chen Eric S.1ORCID,Xiao Sheng1ORCID,Snapper Scott B.3ORCID,Bao Bin4ORCID,An Dingding4ORCID,Blumberg Richard S.5ORCID,Lin Cheng-hui6ORCID,Wang Sui6ORCID,Zhong Jiaxin7ORCID,Liu Kuai7ORCID,Li Qiyuan7ORCID,Wu Chuan12ORCID,Kuchroo Vijay K.18ORCID

Affiliation:

1. Evergrande Center for Immunological Diseases, Harvard Medical School and Brigham and Women’s Hospital, Boston, MA

2. Experimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD

3. Division of Gastroenterology, Hepatology and Nutrition, Boston Children’s Hospital, Boston, MA

4. Department of Pediatrics, Boston Children’s Hospital, Boston, MA

5. Division of Gastroenterology, Hepatology, and Endoscopy, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA

6. Department of Ophthalmology, Mary M. and Sash A. Spencer Center for Vision Research, Byers Eye Institute, Stanford University, Stanford, CA

7. Department of Medicine, School of Medicine, Xiamen University, Xiamen, China

8. Klarman Cell Observatory, Broad Institute of Massachusetts Institute of Technology and Harvard, Cambridge, MA

Abstract

Mucus produced by goblet cells in the gastrointestinal tract forms a biological barrier that protects the intestine from invasion by commensals and pathogens. However, the host-derived regulatory network that controls mucus secretion and thereby changes gut microbiota has not been well studied. Here, we identify that Forkhead box protein O1 (Foxo1) regulates mucus secretion by goblet cells and determines intestinal homeostasis. Loss of Foxo1 in intestinal epithelial cells (IECs) results in defects in goblet cell autophagy and mucus secretion, leading to an impaired gut microenvironment and dysbiosis. Subsequently, due to changes in microbiota and disruption in microbiome metabolites of short-chain fatty acids, Foxo1 deficiency results in altered organization of tight junction proteins and enhanced susceptibility to intestinal inflammation. Our study demonstrates that Foxo1 is crucial for IECs to establish commensalism and maintain intestinal barrier integrity by regulating goblet cell function.

Funder

Crohn’s and Colitis Foundation

American Diabetes Association

National Eye Institute

Research to Prevent Blindness

National Multiple Sclerosis Society

National Institutes of Health

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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