Literature DB >> 11515846

Epithelial expression of caveolin-2, but not caveolin-1, is enhanced in the inflamed mucosa of patients with ulcerative colitis.

A Andoh1, T Saotome, H Sato, T Tsujikawa, Y Araki, Y Fujiyama, T Bamba.   

Abstract

Caveolae are vesicular invaginations of the plasma membrane that act as a scaffold of the assembly of many classes of signaling molecules. Caveolins are the principal structural component of caveolae membranes, and three distinct forms of caveolins have been identified: caveolin-1, caveolin-2, and caveolin-3. In this study, we evaluated the changes in the caveolin-1 and caveolin-2 expression in the inflamed mucosa of patients with IBD. Tissue samples were obtained endoscopically from patients with ulcerative colitis (UC) (n = 18), Crohn's disease (n = 10) and ischemic colitis (n = 8). Normal colorectal tissues were also obtained (n = 15). The caveolin expression was evaluated by standard immunohistochemical procedure. In normal colonic mucosa, caveolin-1 expression was detected in the smooth-muscle cells of the muscularis mucosae and the endothelial cells, but caveolin-2 expression was not detected. In the inflamed mucosa of patients with active UC, caveolin-2 expression was clearly detectable as small scattered foci on the luminal surfaces of epithelial cells, but caveolin-1 expression was similar to that in normal mucosa. Caveolin-2 expression increased in accordance with the disease activity of UC. This enhanced caveolin-2 expression was not detected in active Crohn's disease or ischemic colitis. In conclusion, we demonstrated that the epithelial expression of caveolin-2 is markedly enhanced in the inflamed mucosa of patients with UC. It is likely that the enhanced caveolin-2 expression in patients with UC was associated with the altered signal transductions in the intestinal epithelial cells. Furthermore, our results suggest that there are differences in the phenotypic features of epithelial cells between UC and Crohn's disease.

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Year:  2001        PMID: 11515846     DOI: 10.1097/00054725-200108000-00005

Source DB:  PubMed          Journal:  Inflamm Bowel Dis        ISSN: 1078-0998            Impact factor:   5.325


  7 in total

Review 1.  Regulation of epithelial cell functions by the intestinal milieu.

Authors:  Tadao Bamba
Journal:  J Gastroenterol       Date:  2002-11       Impact factor: 7.527

2.  Biomarkers of human gastrointestinal tract regions.

Authors:  Elena Maria Comelli; Sofiane Lariani; Marie-Camille Zwahlen; Grigorios Fotopoulos; James Anthony Holzwarth; Christine Cherbut; Gian Dorta; Irène Corthésy-Theulaz; Martin Grigorov
Journal:  Mamm Genome       Date:  2009-08-27       Impact factor: 2.957

3.  Caveolin as a potential drug target for cardiovascular protection.

Authors:  Stephanie L Sellers; Andy E Trane; Pascal N Bernatchez
Journal:  Front Physiol       Date:  2012-07-18       Impact factor: 4.566

4.  Sparse Modeling Reveals miRNA Signatures for Diagnostics of Inflammatory Bowel Disease.

Authors:  Matthias Hübenthal; Georg Hemmrich-Stanisak; Frauke Degenhardt; Silke Szymczak; Zhipei Du; Abdou Elsharawy; Andreas Keller; Stefan Schreiber; Andre Franke
Journal:  PLoS One       Date:  2015-10-14       Impact factor: 3.240

Review 5.  Angiogenesis in Inflammatory Bowel Disease.

Authors:  Canan Alkim; Huseyin Alkim; Ali Riza Koksal; Salih Boga; Ilker Sen
Journal:  Int J Inflam       Date:  2015-12-29

6.  Fibrosis Mediators in the Colonic Mucosa of Acute and Healed Ulcerative Colitis.

Authors:  Mona Dixon Gundersen; Rasmus Goll; Christopher Graham Fenton; Endre Anderssen; Sveinung Wergeland Sørbye; Jon Ragnar Florholmen; Ruth Hracky Paulssen
Journal:  Clin Transl Gastroenterol       Date:  2019-10       Impact factor: 4.488

7.  Caveolar communication with xenobiotic-stalled ribosomes compromises gut barrier integrity.

Authors:  Seong-Hwan Park; Juil Kim; Yuseok Moon
Journal:  Commun Biol       Date:  2020-05-27
  7 in total

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