Université Paris-Est Créteil, INSERM, IMRB, 94010 Créteil, France.
Université Paris-Est Créteil, INSERM, IMRB, 94010 Créteil, France; EnvA, IMRB, 94700 Maisons-Alfort, France.
Cell Metab. 2021 Feb 2;33(2):283-299.e9. doi: 10.1016/j.cmet.2020.12.006. Epub 2021 Jan 4.
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.
血小板被认为可以增强间充质干细胞(MSCs)的伤口愈合活性。然而,血小板提高 MSCs 治疗潜力的机制尚未阐明。在这里,我们提供的证据表明,血小板在激活后主要通过依赖于动力蛋白的网格蛋白介导的内吞作用将呼吸功能正常的线粒体转移到 MSCs 中。我们发现,这一过程增强了 MSCs 在几种组织损伤小鼠模型中的植入后的治疗效果,包括全层皮肤伤口和营养不良的骨骼肌。通过体外和体内实验的结合,我们证明了血小板衍生的线粒体通过代谢重编程促进 MSCs 的促血管生成活性。值得注意的是,我们表明,需要激活从头脂肪酸合成途径,才能增加血小板预处理的 MSCs 分泌促血管生成因子。这些结果揭示了血小板增强 MSC 特性的新机制,并强调了在临床应用前测试血小板线粒体质量的重要性。