| Literature DB >> 16508738 |
Roberto Del Bo1, Marina Scarlato, Serena Ghezzi, Anna Maestroni, Lisa Sjölind, Carol Forsblom, Maija Wessman, Per-Henrik Groop, Giacomo Pietro Comi, Nereo Bresolin, Livio Luzi, Gianpaolo Zerbini.
Abstract
Vascular endothelial growth factor (VEGF) is a multifunctional cytokine originally described as an angiogenic factor. A number of reports have recently demonstrated that VEGF increases pancreatic islet survival after islet transplantation by stimulating angiogenesis and improving islet revascularization. Whether VEGF can protect from the autoimmune destruction of insulin-producing beta-cells that characterizes the development of type 1 diabetes is presently unknown. To clarify this issue, we studied the association of three polymorphisms of the promoter region of VEGF with type 1 diabetes in the Italian and the Finnish populations. The polymorphisms considered [C(-2578)A, G(-1190)A, and G(-1154)A] are known to modulate in vitro and in vivo VEGF expression. We found that VEGF promoter genotypes are associated with type 1 diabetes in both populations, but with different combinations. In Italian individuals, the -2578AA and -1190AA genotypes are associated with type 1 diabetes and accelerate its onset, while in Finnish individuals, -1154GG and -1190GG protect from type 1 diabetes and delay its onset. In conclusion, because the expected functional consequence of both genotype combinations is a reduced VEGF expression in diabetic patients, we propose a protective role of VEGF in the development of type 1 diabetes.Entities:
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Year: 2006 PMID: 16508738 DOI: 10.1007/s00251-006-0089-2
Source DB: PubMed Journal: Immunogenetics ISSN: 0093-7711 Impact factor: 2.846