Regulation of glucose-stimulated insulin secretion by ATPase Inhibitory Factor 1 (IF1)
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu dopisy, práce podpořená grantem
PubMed
29380352
DOI
10.1002/1873-3468.12991
Knihovny.cz E-zdroje
- Klíčová slova
- ATP synthase, IF1, INS-1E cells, diabetes, insulin secretion, β-cells,
- MeSH
- beta-buňky cytologie metabolismus MeSH
- glukosa metabolismus MeSH
- inzulin metabolismus MeSH
- krysa rodu Rattus MeSH
- nádorové buněčné linie MeSH
- potkani Wistar MeSH
- protein inhibující ATPasu MeSH
- proteiny metabolismus MeSH
- spotřeba kyslíku fyziologie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- zvířata MeSH
- Publikační typ
- dopisy MeSH
- práce podpořená grantem MeSH
- Názvy látek
- glukosa MeSH
- inzulin MeSH
- proteiny MeSH
ATPase Inhibitory factor 1 (IF1) is an endogenous regulator of mitochondrial ATP synthase, which is involved in cellular metabolism. Although great progress has been made, biological roles of IF1 and molecular mechanisms of its action are still to be elucidated. Here, we show that IF1 is present in pancreatic β-cells, bound to the ATP synthase also under normal physiological conditions. IF1 silencing in model pancreatic β-cells (INS-1E) increases insulin secretion over a range of glucose concentrations. The left-shifted dose-response curve reveals excessive insulin secretion even under low glucose, corresponding to fasting conditions. A parallel increase in cellular respiration and ATP levels is observed. To conclude, our results indicate that IF1 is a negative regulator of insulin secretion involved in pancreatic β-cell glucose sensing.
Citace poskytuje Crossref.org
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Fatty Acid-Stimulated Insulin Secretion vs. Lipotoxicity