| Literature DB >> 26384384 |
Honey Modi1, Cecile Jacovetti2, David Tarussio1, Salima Metref1, Ole D Madsen3, Fu-Ping Zhang4, Pia Rantakari4, Matti Poutanen4, Serge Nef5, Tracy Gorman6, Romano Regazzi2, Bernard Thorens7.
Abstract
Insulin-like growth factor 2 (IGF2), produced and secreted by adult β-cells, functions as an autocrine activator of the β-cell insulin-like growth factor 1 receptor signaling pathway. Whether this autocrine activity of IGF2 plays a physiological role in β-cell and whole-body physiology is not known. Here, we studied mice with β-cell-specific inactivation of Igf2 (βIGF2KO mice) and assessed β-cell mass and function in aging, pregnancy, and acute induction of insulin resistance. We showed that glucose-stimulated insulin secretion (GSIS) was markedly reduced in old female βIGF2KO mice; glucose tolerance was, however, normal because of increased insulin sensitivity. While on a high-fat diet, both male and female βIGF2KO mice displayed lower GSIS compared with control mice, but reduced β-cell mass was observed only in female βIGF2KO mice. During pregnancy, there was no increase in β-cell proliferation and mass in βIGF2KO mice. Finally, β-cell mass expansion in response to acute induction of insulin resistance was lower in βIGF2KO mice than in control mice. Thus, the autocrine action of IGF2 regulates adult β-cell mass and function to preserve in vivo GSIS in aging and to adapt β-cell mass in response to metabolic stress, pregnancy hormones, and acute induction of insulin resistance.Entities:
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Year: 2015 PMID: 26384384 DOI: 10.2337/db14-1735
Source DB: PubMed Journal: Diabetes ISSN: 0012-1797 Impact factor: 9.461