| Literature DB >> 24044104 |
Anna-Maria Ordelheide1, Felicia Gerst, Oliver Rothfuss, Martin Heni, Carina Haas, Inga Thielker, Silke Herzberg-Schäfer, Anja Böhm, Fausto Machicao, Susanne Ullrich, Norbert Stefan, Andreas Fritsche, Hans-Ulrich Häring, Harald Staiger.
Abstract
B-cell failure at the onset of type 2 diabetes is caused by a decline in β-cell function in the postprandial state and loss of pancreatic β-cell mass. Recently, we showed an association between increased insulin secretion and a single nucleotide polymorphism (SNP), SNP rs12686676, in the NR4A3 gene locus encoding the nuclear receptor Nor-1. Nor-1 is expressed in β-cells, however, not much is known about its function with regard to insulin gene expression and insulin secretion. Nor-1 is induced in a glucose-/incretin-dependent manner via the PKA pathway and directly induces insulin gene expression. Additionally, it stimulates insulin secretion possibly via regulation of potentially important genes in insulin exocytosis. Moreover, we show that the minor allele of NR4A3 SNP rs12686676 fully rescues incretin resistance provoked by a well-described polymorphism in TCF7L2. Thus, Nor-1 represents a promising new target for pharmacological intervention to fight diabetes.Entities:
Keywords: Incretin resistance; Insulin gene expression; Insulin secretion; Nor-1; TCF7L2
Year: 2013 PMID: 24044104 PMCID: PMC3773820 DOI: 10.1016/j.molmet.2013.06.003
Source DB: PubMed Journal: Mol Metab ISSN: 2212-8778 Impact factor: 7.422