Platelets Facilitate the Wound-Healing Capability of Mesenchymal Stem Cells by Mitochondrial Transfer and Metabolic Reprogramming
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
33400911
DOI
10.1016/j.cmet.2020.12.006
PII: S1550-4131(20)30661-6
Knihovny.cz E-zdroje
- Klíčová slova
- angiogenesis, cell therapy, citrate, de novo, fatty acid synthesis, intercellular mitochondria transfer, mesenchymal stem cells, metabolism reprogramming, mitochondria, mitochondrial respiration, platelets,
- MeSH
- hojení ran MeSH
- mezenchymální kmenové buňky metabolismus MeSH
- mitochondrie metabolismus MeSH
- myši inbrední C57BL MeSH
- myši transgenní MeSH
- myši MeSH
- trombocyty metabolismus MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Platelets are known to enhance the wound-healing activity of mesenchymal stem cells (MSCs). However, the mechanism by which platelets improve the therapeutic potential of MSCs has not been elucidated. Here, we provide evidence that, upon their activation, platelets transfer respiratory-competent mitochondria to MSCs primarily via dynamin-dependent clathrin-mediated endocytosis. We found that this process enhances the therapeutic efficacy of MSCs following their engraftment in several mouse models of tissue injury, including full-thickness cutaneous wound and dystrophic skeletal muscle. By combining in vitro and in vivo experiments, we demonstrate that platelet-derived mitochondria promote the pro-angiogenic activity of MSCs via their metabolic remodeling. Notably, we show that activation of the de novo fatty acid synthesis pathway is required for increased secretion of pro-angiogenic factors by platelet-preconditioned MSCs. These results reveal a new mechanism by which platelets potentiate MSC properties and underline the importance of testing platelet mitochondria quality prior to their clinical use.
Institute of Biotechnology Czech Academy of Sciences 252 50 Prague West Prague Czech Republic
Université de Paris Institut Cochin INSERM CNRS 75014 Paris France
Université Paris Est Créteil INSERM IMRB 94010 Créteil France
Université Paris Est Créteil INSERM IMRB 94010 Créteil France; EnvA IMRB 94700 Maisons Alfort France
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