Mucins: a biologically relevant glycan barrier in mucosal protection
- PMID: 24821013
- DOI: 10.1016/j.bbagen.2014.05.003
Mucins: a biologically relevant glycan barrier in mucosal protection
Abstract
Background: The mucins found as components of mucus gel layers at mucosal surfaces throughout the body play roles in protection as part of the defensive barrier on an organ and tissue specific basis.
Scope of the review: The human MUC gene family codes up to 20 known proteins, which can be divided into secreted and membrane-associated forms each with a typical protein domain structure. The secreted mucins are adapted to cross link in order to allow formation of the extended mucin networks found in the secreted mucus gels. The membrane-associated mucins possess membrane specific domains which enable their various biological functions as part of the glycocalyx. All mucins are highly O-glycosylated and this is tissue specific and linked with specific biological functions at these locations. Mucin biology is dynamic and the processes of degradation and turnover are well integrated with biosynthesis to maintain a continuous mucosal protection against all external aggressive forces. Interaction of mucins with microflora plays an important role in normal function. Mucins are modified in a variety of diseases and this may be due to abberant mucin peptide or glycosylation.
Major conclusions: Mucins represent a family of glycoprotein having fundamental roles in mucosal protection and communication with external environment.
General significance: The review emphasises the nature of mucins as glycoproteins and their role in presenting an array of glycan structures at the mucosal cell surface.
Keywords: Cancer; Glycosylation; Microflora; Mucin; Mucosal; Mucus.
Copyright © 2014 Elsevier B.V. All rights reserved.
Similar articles
-
Mucins in the gastrointestinal tract in health and disease.Front Biosci. 2001 Oct 1;6:D1321-57. doi: 10.2741/corfield. Front Biosci. 2001. PMID: 11578958 Review.
-
Mucus and Mucins: The Underappreciated Host Defence System.Front Cell Infect Microbiol. 2022 Jun 14;12:856962. doi: 10.3389/fcimb.2022.856962. eCollection 2022. Front Cell Infect Microbiol. 2022. PMID: 35774401 Free PMC article. Review.
-
Mucin-type O-glycans and their roles in intestinal homeostasis.Glycobiology. 2013 Sep;23(9):1026-37. doi: 10.1093/glycob/cwt045. Epub 2013 Jun 10. Glycobiology. 2013. PMID: 23752712 Free PMC article. Review.
-
Transmembrane Mucins: Signaling Receptors at the Intersection of Inflammation and Cancer.J Innate Immun. 2017;9(3):281-299. doi: 10.1159/000453594. Epub 2017 Jan 5. J Innate Immun. 2017. PMID: 28052300 Free PMC article. Review.
-
Management of the human mucosal defensive barrier: evidence for glycan legislation.Biol Chem. 2009 Jul;390(7):581-90. doi: 10.1515/BC.2009.052. Biol Chem. 2009. PMID: 19335202 Review.
Cited by
-
Conserved signaling modules regulate filamentous growth in fungi: a model for eukaryotic cell differentiation.Genetics. 2024 Oct 7;228(2):iyae122. doi: 10.1093/genetics/iyae122. Genetics. 2024. PMID: 39239926 Review.
-
Emergence of MUC1 in Mammals for Adaptation of Barrier Epithelia.Cancers (Basel). 2022 Sep 30;14(19):4805. doi: 10.3390/cancers14194805. Cancers (Basel). 2022. PMID: 36230728 Free PMC article. Review.
-
Assessing Bacterial Interactions Using Carbohydrate-Based Microarrays.Microarrays (Basel). 2015 Dec 10;4(4):690-713. doi: 10.3390/microarrays4040690. Microarrays (Basel). 2015. PMID: 27600247 Free PMC article. Review.
-
Revealing biomedically relevant cell and lectin type-dependent structure-activity profiles for glycoclusters by using tissue sections as an assay platform.RSC Adv. 2018 Aug 14;8(50):28716-28735. doi: 10.1039/c8ra05382k. eCollection 2018 Aug 7. RSC Adv. 2018. PMID: 35542469 Free PMC article.
-
Elucidating the Role of Innate and Adaptive Immune Responses in the Pathogenesis of Canine Chronic Inflammatory Enteropathy-A Search for Potential Biomarkers.Animals (Basel). 2022 Jun 27;12(13):1645. doi: 10.3390/ani12131645. Animals (Basel). 2022. PMID: 35804545 Free PMC article. Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Research Materials