| Literature DB >> 27185156 |
Tiinamaija Tuomi1, Cecilia L F Nagorny2, Pratibha Singh2, Hedvig Bennet3, Qian Yu4, Ida Alenkvist4, Bo Isomaa5, Bjarne Östman6, Johan Söderström7, Anu-Katriina Pesonen8, Silja Martikainen8, Katri Räikkönen8, Tom Forsén6, Liisa Hakaste9, Peter Almgren10, Petter Storm11, Olof Asplund11, Liliya Shcherbina12, Malin Fex3, João Fadista11, Anders Tengholm4, Nils Wierup12, Leif Groop13, Hindrik Mulder14.
Abstract
Type 2 diabetes (T2D) is a global pandemic. Genome-wide association studies (GWASs) have identified >100 genetic variants associated with the disease, including a common variant in the melatonin receptor 1 b gene (MTNR1B). Here, we demonstrate increased MTNR1B expression in human islets from risk G-allele carriers, which likely leads to a reduction in insulin release, increasing T2D risk. Accordingly, in insulin-secreting cells, melatonin reduced cAMP levels, and MTNR1B overexpression exaggerated the inhibition of insulin release exerted by melatonin. Conversely, mice with a disruption of the receptor secreted more insulin. Melatonin treatment in a human recall-by-genotype study reduced insulin secretion and raised glucose levels more extensively in risk G-allele carriers. Thus, our data support a model where enhanced melatonin signaling in islets reduces insulin secretion, leading to hyperglycemia and greater future risk of T2D. The findings also imply that melatonin physiologically serves to inhibit nocturnal insulin release.Entities:
Keywords: RNA sequencing; gene targeting; insulin; islets; recall-by-genotype
Mesh:
Substances:
Year: 2016 PMID: 27185156 DOI: 10.1016/j.cmet.2016.04.009
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287