间充质干细胞
伤口愈合
细胞生物学
血小板
线粒体
血小板活化
干细胞
生物
癌症研究
免疫学
作者
Jennyfer Levoux,Alexandre Prola,Peggy Lafuste,Marianne Gervais,Nathalie Chevallier,Zeynab Koumaiha,Kaouthar Kefi,Laura Braud,Alain Schmitt,Azzedine Yacia,Aurélie Schirmann,Barbara Hersant,Mounia Sid-Ahmed,Sabrina Ben Larbi,Kateřina Komrsková,Jakub Rohlena,Frédéric Relaix,Jiřı́ Neužil,Anne‐Marie Rodriguez
出处
期刊:Cell Metabolism
[Elsevier]
日期:2021-01-10
卷期号:33 (2): 283-299.e9
被引量:148
标识
DOI:10.1016/j.cmet.2020.12.006
摘要
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.
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