期刊
JOURNAL OF BIOLOGICAL CHEMISTRY
卷 290, 期 3, 页码 1456-1473出版社
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M114.616763
关键词
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资金
- National Institutes of Health [R01CA043796, RO1 DE010389, CA062948]
- Weill Cornell funds
We show that vitamin A (all-trans-retinol) (VA) is required both for the maintenance of pancreatic beta-cell and alpha-cell mass and for glucose-stimulated insulin secretion in adult mice. Dietary VA deprivation (VAD) causes greatly decreased pancreatic VA levels, hyperglycemia, and reduced insulin secretion. Adult mice fed VAD diets display remodeling of the endocrine pancreas, marked beta-cell apoptosis, shifts to smaller islet size distributions, decreased beta-cell mass, increased alpha-cell mass, and hyperglucagonemia. Importantly, although we induced VAD in the entire animal, the pancreatic beta-cells are exquisitely sensitive to VAD-associated apoptosis compared with other cell types in other organs. VAD causes major reductions in levels of the VA intracellular binding protein Crbp1 and the retinoic acid-metabolizing enzyme Cyp26a1 specifically in larger islets, suggesting the use of these proteins as biomarkers for early endocrine mass abnormalities. In the VAD mice, the reductions in pancreatic islet sizes and the associated aberrant endocrine functions, which show similarities to the phenotype in advanced type 2 diabetes, result from reductions in pancreatic VA signaling. Reintroduction of dietary VA to VAD mice restores pancreatic VA levels, glycemic control, normal islet size distributions, beta-cell to alpha-cell ratios, endocrine hormone profiles, and RAR beta 2 and RAR gamma 2 transcript levels. Restoration of beta-cell mass by reintroducing VA to VAD mice does not involve increased beta-cell proliferation or neogenesis. Pharmacologic modulation of pancreatic VA signaling should be explored for the preservation and/or restoration of pancreatic beta-cell mass and function in individuals with diabetes mellitus.
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