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Aglycemia triggers alternative electron transport to sustain mesenchymal stem cell survival under anoxia.

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Title: Aglycemia triggers alternative electron transport to sustain mesenchymal stem cell survival under anoxia.
Authors: Refeyton A; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France; Children's Hospital of Philadelphia, Philadelphia, USA., Amoedo ND; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France., Labat V; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France., Vignane T; Leibniz Institute for Analytical Sciences, ISAS e.V., Dortmund, Germany; Institute of Molecular Systems Medicine, Goethe University of Frankfurt, Faculty of Medicine, Frankfurt, Germany., Buré C; Service Analyses Métaboliques-TBMCore University of Bordeaux, UAR CNRS 3427, US05 INSERM, France., Pinson B; Service Analyses Métaboliques-TBMCore University of Bordeaux, UAR CNRS 3427, US05 INSERM, France; Institute of Cellular Biochemistry and Genetics, UMR 5095 CNRS, University of Bordeaux, France., Ley-Ngardigal S; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France., Debeissat C; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France., Bursac B; Institute of Cellular Biochemistry and Genetics, UMR 5095 CNRS, University of Bordeaux, France; Department of Biochemistry, Institute for Biological Research, University of Belgrade, Serbia., Claverol S; University of Bordeaux, Bordeaux Proteome, Bordeaux, France., Khelifi R; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France., Rodriguez L; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France., de la Grange PB; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France., Rossignol R; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France., Filipovic MR; Leibniz Institute for Analytical Sciences, ISAS e.V., Dortmund, Germany; Institute of Cellular Biochemistry and Genetics, UMR 5095 CNRS, University of Bordeaux, France; School of Molecular Biosciences, University of Glasgow, Scotland, UK. Electronic address: Milos.Filipovic@glasgow.ac.uk., Ivanovic Z; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France. Electronic address: Zoran.ivanovic@efs.sante.fr., Vlaski-Lafarge M; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France. Electronic address: Marija.vlaski@efs.sante.fr.
Source: Redox biology [Redox Biol] 2026 Jul 14; Vol. 96, pp. 104304. Date of Electronic Publication: 2026 Jul 14.
Publication Type: Journal Article
Journal Info: Publisher: Elsevier, B.V Country of Publication: Netherlands NLM ID: 101605639 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2213-2317 (Electronic) Linking ISSN: 22132317 NLM ISO Abbreviation: Redox Biol Subsets: MEDLINE
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  Data: Aglycemia triggers alternative electron transport to sustain mesenchymal stem cell survival under anoxia.
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  Data: <searchLink fieldCode="AU" term="%22Refeyton+A%22">Refeyton A</searchLink>; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France; Children's Hospital of Philadelphia, Philadelphia, USA.<br /><searchLink fieldCode="AU" term="%22Amoedo+ND%22">Amoedo ND</searchLink>; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France.<br /><searchLink fieldCode="AU" term="%22Labat+V%22">Labat V</searchLink>; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France.<br /><searchLink fieldCode="AU" term="%22Vignane+T%22">Vignane T</searchLink>; Leibniz Institute for Analytical Sciences, ISAS e.V., Dortmund, Germany; Institute of Molecular Systems Medicine, Goethe University of Frankfurt, Faculty of Medicine, Frankfurt, Germany.<br /><searchLink fieldCode="AU" term="%22Buré+C%22">Buré C</searchLink>; Service Analyses Métaboliques-TBMCore University of Bordeaux, UAR CNRS 3427, US05 INSERM, France.<br /><searchLink fieldCode="AU" term="%22Pinson+B%22">Pinson B</searchLink>; Service Analyses Métaboliques-TBMCore University of Bordeaux, UAR CNRS 3427, US05 INSERM, France; Institute of Cellular Biochemistry and Genetics, UMR 5095 CNRS, University of Bordeaux, France.<br /><searchLink fieldCode="AU" term="%22Ley-Ngardigal+S%22">Ley-Ngardigal S</searchLink>; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France.<br /><searchLink fieldCode="AU" term="%22Debeissat+C%22">Debeissat C</searchLink>; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France.<br /><searchLink fieldCode="AU" term="%22Bursac+B%22">Bursac B</searchLink>; Institute of Cellular Biochemistry and Genetics, UMR 5095 CNRS, University of Bordeaux, France; Department of Biochemistry, Institute for Biological Research, University of Belgrade, Serbia.<br /><searchLink fieldCode="AU" term="%22Claverol+S%22">Claverol S</searchLink>; University of Bordeaux, Bordeaux Proteome, Bordeaux, France.<br /><searchLink fieldCode="AU" term="%22Khelifi+R%22">Khelifi R</searchLink>; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France.<br /><searchLink fieldCode="AU" term="%22Rodriguez+L%22">Rodriguez L</searchLink>; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France.<br /><searchLink fieldCode="AU" term="%22de+la+Grange+PB%22">de la Grange PB</searchLink>; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France.<br /><searchLink fieldCode="AU" term="%22Rossignol+R%22">Rossignol R</searchLink>; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France.<br /><searchLink fieldCode="AU" term="%22Filipovic+MR%22">Filipovic MR</searchLink>; Leibniz Institute for Analytical Sciences, ISAS e.V., Dortmund, Germany; Institute of Cellular Biochemistry and Genetics, UMR 5095 CNRS, University of Bordeaux, France; School of Molecular Biosciences, University of Glasgow, Scotland, UK. Electronic address: Milos.Filipovic@glasgow.ac.uk.<br /><searchLink fieldCode="AU" term="%22Ivanovic+Z%22">Ivanovic Z</searchLink>; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France. Electronic address: Zoran.ivanovic@efs.sante.fr.<br /><searchLink fieldCode="AU" term="%22Vlaski-Lafarge+M%22">Vlaski-Lafarge M</searchLink>; Etablissement Français du Sang, Nouvelle Aquitaine, France; Rare disease genetics and metabolism, Inserm U1211, University of Bordeux, France. Electronic address: Marija.vlaski@efs.sante.fr.
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  Data: <searchLink fieldCode="JN" term="%22101605639%22">Redox biology</searchLink> [Redox Biol] 2026 Jul 14; Vol. 96, pp. 104304. <i>Date of Electronic Publication: </i>2026 Jul 14.
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