Abstract
Pregnancy and obesity are frequently associated with diminished insulin sensitivity, which is normally compensated for by an expansion of the functional β cell mass that prevents chronic hyperglycemia and development of diabetes mellitus. The molecular basis underlying compensatory β cell mass expansion is largely unknown. We found in rodents that β cell mass expansion during pregnancy and obesity is associated with changes in the expression of several islet microRNAs, including miR-338-3p. In isolated pancreatic islets, we recapitulated the decreased miR-338-3p level observed in gestation and obesity by activating the G protein-coupled estrogen receptor GPR30 and the glucagon-like peptide 1 (GLP1) receptor. Blockade of miR-338-3p in β cells using specific anti-miR molecules mimicked gene expression changes occurring during β cell mass expansion and resulted in increased proliferation and improved survival both in vitro and in vivo. These findings point to a major role for miR-338-3p in compensatory β cell mass expansion occurring under different insulin resistance states.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adaptation, Physiological / physiology*
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Animals
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Cells, Cultured / drug effects
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Cells, Cultured / metabolism
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Cytokines / biosynthesis
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Cytokines / genetics
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Estradiol / analogs & derivatives
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Estradiol / pharmacology
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Estradiol / physiology
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Estrogen Antagonists / pharmacology
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Female
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Fulvestrant
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Gene Expression Regulation / physiology
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Glucagon-Like Peptide 1 / physiology
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Glucagon-Like Peptide-1 Receptor
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Insulin Resistance / physiology*
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Islets of Langerhans / growth & development*
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Islets of Langerhans / metabolism
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Islets of Langerhans / pathology*
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Male
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Mice
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Mice, Mutant Strains
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MicroRNAs / biosynthesis
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MicroRNAs / genetics
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MicroRNAs / physiology*
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Obesity / pathology*
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Obesity / physiopathology
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Organ Size / drug effects
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Postpartum Period / metabolism
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Pregnancy / metabolism
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Pregnancy / physiology*
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Rats
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Rats, Wistar
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Receptors, G-Protein-Coupled / agonists
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Receptors, G-Protein-Coupled / biosynthesis
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Receptors, G-Protein-Coupled / genetics
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Receptors, Glucagon / agonists
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Receptors, Glucagon / deficiency
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Signal Transduction / drug effects
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Signal Transduction / physiology
Substances
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Cytokines
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Estrogen Antagonists
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Glp1r protein, mouse
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Glp1r protein, rat
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Glucagon-Like Peptide-1 Receptor
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Gper1 protein, rat
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MIRN144 microRNA, rat
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MIRN338 microRNA, rat
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MIRN451A microRNA, rat
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MicroRNAs
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Receptors, G-Protein-Coupled
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Receptors, Glucagon
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Fulvestrant
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Estradiol
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Glucagon-Like Peptide 1