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Abstract
Metabolite alteration has been associated with the pathogenesis of inflammatory bowel disease (IBD), including colitis. Mannose, a natural bioactive monosaccharide that is involved in metabolism and synthesis of glycoproteins, exhibits anti-inflammatory and anti-oxidative activities. We show here that the circulating level of mannose is increased in patients with IBD and mice with experimental colitis. Mannose treatment attenuates intestinal barrier damage in two mouse colitis models, dextran sodium sulfate (DSS)-induced colitis and spontaneous colitis in IL-10-deficient mice. We demonstrate that mannose treatment enhanced lysosomal integrity and limited the release of cathepsin B, preventing mitochondrial dysfunction and myosin light chain kinase (MLCK)-induced tight junction disruption in the context of intestinal epithelial damage. Mannose exerts a synergistic therapeutic effect with mesalamine on mouse colitis. Cumulatively, the results indicate that mannose supplementation may be an optional approach to the treatment of colitis and other diseases associated with intestinal barrier dysfunction.
New potential therapies for inflammatory bowel disease are needed as not all patients respond to or maintain a response to conventional therapies. Here the authors report that mannose supplementation ameliorates experimental colitis in male mice, potentially via effects on intestinal epithelium lysosomal integrity.
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1 Southern Medical University, The Fifth Affiliated Hospital, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471); Southern Medical University, Department of Medical Laboratory, School of Laboratory Medicine and Biotechnology, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471); Southern Medical University, Guangdong Provincial Key Laboratory of Proteomics, Department of Immunology, School of Basic Medical Sciences, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471)
2 Southern Medical University, Department of Medical Laboratory, School of Laboratory Medicine and Biotechnology, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471); Southern Medical University, Guangdong Provincial Key Laboratory of Proteomics, Department of Immunology, School of Basic Medical Sciences, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471)
3 Southern Medical University, Guangdong Provincial Key Laboratory of Proteomics, Department of Immunology, School of Basic Medical Sciences, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471)
4 Southern Medical University, Department of Gastroenterology, Nanfang Hospital, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471)
5 Zhejiang University School of Medicine, Institute of Immunology, Hangzhou, China (GRID:grid.13402.34) (ISNI:0000 0004 1759 700X)
6 Southern Medical University, The Fifth Affiliated Hospital, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471)
7 Virginia Commonwealth University, Department of Human and Molecular Genetics, Richmond, USA (GRID:grid.224260.0) (ISNI:0000 0004 0458 8737)
8 Southern Medical University, The Fifth Affiliated Hospital, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471); Southern Medical University, Department of Medical Laboratory, School of Laboratory Medicine and Biotechnology, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471); Southern Medical University, Microbiome Medicine Center, Zhujiang Hospital, Guangzhou, China (GRID:grid.284723.8) (ISNI:0000 0000 8877 7471)