Mitochondria to plasma membrane redox signaling is essential for fatty acid β-oxidation-driven insulin secretion
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
39067330
PubMed Central
PMC11332078
DOI
10.1016/j.redox.2024.103283
PII: S2213-2317(24)00261-1
Knihovny.cz E-zdroje
- Klíčová slova
- Fatty acid-stimulated insulin secretion, GPR40, Mitochondrial fatty acids, Pancreatic β-cells, Redox signaling, Redox-activated phospholipase iPLA2γ,
- MeSH
- beta-buňky * metabolismus MeSH
- buněčná membrána * metabolismus MeSH
- fosfolipasy A2, skupina VI metabolismus genetika MeSH
- glukosa metabolismus MeSH
- inzulin metabolismus MeSH
- mastné kyseliny * metabolismus MeSH
- mitochondrie * metabolismus MeSH
- myši knockoutované MeSH
- myši MeSH
- oxidace-redukce * MeSH
- peroxid vodíku metabolismus MeSH
- receptory spřažené s G-proteiny MeSH
- sekrece inzulinu * MeSH
- signální transdukce * MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- Ffar1 protein, mouse MeSH Prohlížeč
- fosfolipasy A2, skupina VI MeSH
- glukosa MeSH
- inzulin MeSH
- mastné kyseliny * MeSH
- peroxid vodíku MeSH
- Pla2g6 protein, mouse MeSH Prohlížeč
- receptory spřažené s G-proteiny MeSH
We asked whether acute redox signaling from mitochondria exists concomitantly to fatty acid- (FA-) stimulated insulin secretion (FASIS) at low glucose by pancreatic β-cells. We show that FA β-oxidation produces superoxide/H2O2, providing: i) mitochondria-to-plasma-membrane redox signaling, closing KATP-channels synergically with elevated ATP (substituting NADPH-oxidase-4-mediated H2O2-signaling upon glucose-stimulated insulin secretion); ii) activation of redox-sensitive phospholipase iPLA2γ/PNPLA8, cleaving mitochondrial FAs, enabling metabotropic GPR40 receptors to amplify insulin secretion (IS). At fasting glucose, palmitic acid stimulated IS in wt mice; palmitic, stearic, lauric, oleic, linoleic, and hexanoic acids also in perifused pancreatic islets (PIs), with suppressed 1st phases in iPLA2γ/PNPLA8-knockout mice/PIs. Extracellular/cytosolic H2O2-monitoring indicated knockout-independent redox signals, blocked by mitochondrial antioxidant SkQ1, etomoxir, CPT1 silencing, and catalase overexpression, all inhibiting FASIS, keeping ATP-sensitive K+-channels open, and diminishing cytosolic [Ca2+]-oscillations. FASIS in mice was a postprandially delayed physiological event. Redox signals of FA β-oxidation are thus documented, reaching the plasma membrane, essentially co-stimulating IS.
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