Increased vimentin in human α- and β-cells in type 2 diabetes

Autor: Anne Clark, Alexander Hamilton, Melissa F. Brereton, Michael Verschoor, Joanna M Williams Durkin, Laura J. McCulloch, Eelco J.P. de Koning, F. Carlotti, M. Engelse, Hannah J. Wills, Kevin Docherty, Maaike M Roefs, Laura Garcia-Perez, Barbara C. Hansen, Katherine Elizabeth Jones, Paul Johnson
Přispěvatelé: Hubrecht Institute for Developmental Biology and Stem Cell Research
Rok vydání: 2017
Předmět:
Zdroj: The Journal of endocrinology, 233(3), 217-227. Society for Endocrinology
ISSN: 1479-6805
0022-0795
DOI: 10.1530/joe-16-0588
Popis: Type 2 diabetes (T2DM) is associated with pancreatic islet dysfunction. Loss of β-cell identity has been implicated via dedifferentiation or conversion to other pancreatic endocrine cell types. How these transitions contribute to the onset and progression of T2DM in vivo is unknown. The aims of this study were to determine the degree of epithelial-to-mesenchymal transition occurring in α and β cells in vivo and to relate this to diabetes-associated (patho)physiological conditions. The proportion of islet cells expressing the mesenchymal marker vimentin was determined by immunohistochemistry and quantitative morphometry in specimens of pancreas from human donors with T2DM (n = 28) and without diabetes (ND, n = 38) and in non-human primates at different stages of the diabetic syndrome: normoglycaemic (ND, n = 4), obese, hyperinsulinaemic (HI, n = 4) and hyperglycaemic (DM, n = 8). Vimentin co-localised more frequently with glucagon (α-cells) than with insulin (β-cells) in the human ND group (1.43% total α-cells, 0.98% total β-cells, median; P P P
Databáze: OpenAIRE