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dc.contributor.authorNyström, Elisabeth
dc.date.accessioned2018-10-05T06:43:08Z
dc.date.available2018-10-05T06:43:08Z
dc.date.issued2018-10-05
dc.identifier.isbn978-91-7833-130-7 (PDF)
dc.identifier.urihttp://hdl.handle.net/2077/56886
dc.description.abstractThe mucus layer covering the colonic epithelium creates a crucial first line of defense against the gut residing bacteria. Several lines of evidence suggest that a functional mucus layer is essential for health. For example, it is. suggested that ulcerative colitis is correlated with mucus layer defects. The barrier properties of colonic mucus are partly achieved by creating a dense gel with the MUC2 gel-forming mucin as scaffold. Available MUC2 biochemical and histological data suggest that the mucus is highly structured and organized. Mucus homeostasis is dependent on production, secretion and processing of mucus components. Thus, factors such as goblet cell differentiation, secretory capacity of different cells, and the presence of mucus degrading proteases can affect mucus properties. However, a detailed understanding of mucus structure and processing in vivo is lacking. We have now further developed an existing ex vivo system to study the mucus structure at the microscopic level, as well as investigate the involvement of subpopulations of goblet cells in mucus secretion. This ex vivo method was also used for studies of mucus proteolytic processing by CLCA1, an abundant protease within the mucus. The results suggest that the colonic mucus gel is heterogeneous due to the presence of different goblet cell populations that secrete mucus with different properties. Furthermore, proteolytic processing of MUC2 by CLCA1 is involved in baseline mucus dynamics. Increased understanding of mucus structure and processing is important for future development of pharmacological interventions to improve barrier function in ulcerative colitis and prevent mucus stagnation in diseases such as asthma, chronic obstructive lung disease and cystic fibrosis.sv
dc.language.isoengsv
dc.relation.haspartErickson NA *, Nyström EEL *, Mundhenk L, Arike L, Glauben R, Heimestaat MM, Fischer A, Bereswill S, Bircheough GMH, Grüber AD, Johansson MEV The Goblet Cell Protein Clca1 (Alias mClca3 or Gob-5) Is Not Required for Intestinal Mucus Synthesis, Structure and Barrier Function in Naive or DSS-Challenged Mice. PLOS ONE. 2015; 10(7):e0131991 ::doi::10.1371/journal.pone.0131991sv
dc.relation.haspartNyström EEL, Birchenough GMH, van der Post S, Arike L, Gruber AD, Hansson GC, Johansson MEV Calcium-activated Chloride Channel Regulator 1 (CLCA1) Controls Mucus Expansion in Colon by Proteolytic Activity. EBioMedicine, 2018, 33:134-143 ::doi::10.1016/j.ebiom.2018.05.031sv
dc.relation.haspartNyström EEL, Arike L, Recktenwald CV, Hansson GC, Johansson MEV CLCA1 forms non-covalent oligomers in colonic mucus and has MUC2-processing properties Manuscriptsv
dc.relation.haspartNyström EEL, Martinez Abad B, Eklund L, Birchenough GMH, Johansson MEV Mucus secreted from intercrypt goblet cells is required for proper mucus layer formation in the distal colon and protection against colitis Manuscriptsv
dc.subjectMucussv
dc.subjectCLCA1sv
dc.subjectGoblet cellsv
dc.subjectSpdefsv
dc.titleColonic mucus structure and processingsv
dc.typetexteng
dc.type.svepDoctoral thesiseng
dc.gup.mailelisabeth.nystrom@gu.sesv
dc.type.degreeDoctor of Philosophy (Medicine)sv
dc.gup.originUniversity of Gothenburg. Sahlgrenska Academysv
dc.gup.departmentInstitute of Biomedicine. Department of Medical Biochemistry and Cell Biologysv
dc.gup.defenceplace13.00. Arvid Carlsson, Medicinaregatan 3sv
dc.gup.defencedate2018-10-26
dc.gup.dissdb-fakultetSA


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