Mucin-Type O-Glycans: Barrier, Microbiota, and Immune Anchors in Inflammatory Bowel Disease

被引:25
|
作者
Zhang, Yaqin [1 ]
Wang, Lan [2 ]
Ocansey, Dickson Kofi Wiredu [1 ,3 ]
Wang, Bo [1 ]
Wang, Li [4 ]
Xu, Zhiwei [1 ]
机构
[1] Jiangsu Univ, Sch Med, Key Lab Med Sci & Lab Med Jiangsu Prov, Zhenjiang 212013, Jiangsu, Peoples R China
[2] Danyang Blood Stn, Zhenjiang 212300, Jiangsu, Peoples R China
[3] Univ Cape Coast, Directorate Univ Hlth Serv, Cape Coast, Ghana
[4] Huaian Matern & Children Hosp, 104 Renmin Rd, Huaian 223200, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
glycans; inflammation; intestinal mucus; MUC2; microbiota; immunity; CHAIN FATTY-ACID; GUT MICROBIOTA; MUCUS BARRIER; GOBLET CELLS; AKKERMANSIA-MUCINIPHILA; SPONTANEOUS COLITIS; GENE-EXPRESSION; GLYCOSYLATION; COLON; CANCER;
D O I
10.2147/JIR.S327609
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Inflammatory bowel disease (IBD), which affects about 7 million people globally, is a chronic inflammatory condition of the gastrointestinal tract caused by gut microbiota alterations, immune dysregulation, and genetic and environmental factors. The association of microbial and immune molecules with mucin-type O-glycans has been increasingly noticed by researchers. Mucin is the main component of mucus, which forms a protective barrier between the microbiota and immune cells in the colon. Mucin-type O-glycans alter the diversity of gastrointestinal microorganisms, which in turn increases the level of O-glycosylation of host intestinal proteins via the utilization of glycans. Additionally, alterations in mucin-type O-glycans not only increase the activity and stability of immune cells but are also involved in the maintenance of intestinal mucosal immune tolerance. Although there is accumulating evidence indicating that mucin-type O-glycans play an important role in IBD, there is limited literature that integrates available data to present a complete picture of exactly how O-glycans affect IBD. This review emphasizes the roles of the mucin-type O-glycans in IBD. This seeks to provide a better understanding and encourages future studies on IBD glycosylation and the design of novel glycan-inspired therapies for IBD.
引用
收藏
页码:5939 / 5953
页数:15
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