Relevance of MUC1 mucin variable number of tandem repeats polymorphism in H pylori adhesion to gastric epithelial cells

• Tipo: Artigo em Revista Científica Internacional
• Data: 2008

Autores

Costa, NR (Autor) Outra; Mendes, N (Autor) Outra; Marcos, NT (Autor) Outra; Celso Reis (Autor) FMUP; Caffrey, T (Autor) Outra; Hollingsworth, MA (Autor) Outra; Santos-Silva F (Autor) FMUP

Revista

Título: World Journal of Gastroenterology

Vol. 14 Nº 9

Páginas: 1411-1414

ISSN: 1007-9327

Editora: Baishideng Publishing Group

Indexação

ISI Web of Knowledge - 20 Citações

Scopus - 24 Citações

Outras Informações

ID Authenticus: P-004-0XM

DOI: 10.3748/wjg.14.1411

Abstract (EN): AIM: To evaluate the influence of MUC1 mucin variable number of tandem repeats (VNTR) variability on H pylori adhesion to gastric cells. METHODS: Enzyme linked immunosorbent assay (ELISA)-based adhesion assays were performed to measure the adhesion of different H pylori strains (HP26695 and HPTx30a) to gastric carcinoma cell lines (GP202 and MKN45) and GP202 clones expressing recombinant MUC1 with different VNTR lengths. RESULTS: Evaluation of adhesion results shows that H pylori pathogenic strain HP26695 has a significantly higher (P < 0.05) adhesion to all the cell lines and clones tested, when compared to the non-pathogenic strain HPTx30a. Bacteria showed a significantly higher (P < 0.05) adhesion to the GP202 cell line, when compared to the MKN45 cell line. Furthermore, both strains showed a significantly higher (P < 0.05) adhesion to GP202 clones with larger MUC1 VNTR domains. CONCLUSION: This work shows that MUC1 mucin variability conditions H pylori binding to gastric cells. The extent of bacterial adhesion depends on the size of the MUC1 VNTR domain. The adhesion is further dependent on bacterial pathogenicity and the gastric cell line. MUC1 mucin variability may contribute to determine H pylori colonization of the gastric mucosa.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 4