Innate mechanism of mucosal barrier erosion in the pathogenesis of acquired colitis
Year: 2023
Type: article
Abstract: The colonic mucosal barrier protects against infection, inflammation, and tissue ulceration. Composed primarily of Mucin-2, proteolytic erosion of this barrier is an invariant feature of colitis; however, the molecular mechanisms are not well understood. We have applied a recurrent food poisoning model of acquired inflammatory bowel disease using Salmonella enterica Typhimurium to investigate mucosal barrier erosion. Our findings reveal an innate Toll-like receptor 4-dependent mechanism activated by previous infection that induces Neu3 neuraminidase among colonic epithelial cells concurrent with increased Cathepsin-G protease secretion by Paneth cells. These anatomically separated host responses merge with the desialylation of nascent colonic Mucin-2 by Neu3 rendering the mucosal barrier susceptible to increased proteolytic breakdown by Cathepsin-G. Depletion of Cathepsin-G or Neu3 function using pharmacological inhibitors or genetic-null alleles protected against Mucin-2 proteolysis and barrier erosion and reduced the frequency and severity of colitis, revealing approaches to preserve and potentially restore the mucosal barrier.
Source: iScience
Language: English
Topic: Inflammatory Bowel Disease
Subfield: Gastroenterology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $3,150
Funders: Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Research Foundation, Yonsei University, Ministry of Science, ICT and Future Planning, National Research Foundation of Korea, Ministry of Science ICT and Future Planning, National Institutes of Health, National Heart, Lung, and Blood Institute, National Cancer Institute, National Institute of Allergy and Infectious Diseases, National Institute of Diabetes and Digestive and Kidney Diseases
Awards: G1278561419, G1419972308, G1599927933, G2977429937, G3076074013, G3968701066, G5057194353, G6081178080, Cancer Center Support Grant (CCSG), Protein Sialylation and De-Sialyation in Cell Surface Glycoprotein Homeostasis and Disease, Protein Glycosylation in the Coagulopathy and Inflammation of Sepsis, Glycosyltransferase Function in Development and Disease
OpenAlex ID: W4386569929
