Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Department of Oncology, Division of Molecular Oncology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Nat Commun. 2023 May 22;14(1):2900. doi: 10.1038/s41467-023-38624-0.
Skeletal muscle regeneration involves coordinated interactions between different cell types. Injection of platelet-rich plasma is circumstantially considered an aid to muscle repair but whether platelets promote regeneration beyond their role in hemostasis remains unexplored. Here, we find that signaling via platelet-released chemokines is an early event necessary for muscle repair in mice. Platelet depletion reduces the levels of the platelet-secreted neutrophil chemoattractants CXCL5 and CXCL7/PPBP. Consequently, early-phase neutrophil infiltration to injured muscles is impaired whereas later inflammation is exacerbated. Consistent with this model, neutrophil infiltration to injured muscles is compromised in male mice with Cxcl7-knockout platelets. Moreover, neo-angiogenesis and the re-establishment of myofiber size and muscle strength occurs optimally in control mice post-injury but not in Cxcl7ko mice and in neutrophil-depleted mice. Altogether, these findings indicate that platelet-secreted CXCL7 promotes regeneration by recruiting neutrophils to injured muscles, and that this signaling axis could be utilized therapeutically to boost muscle regeneration.
骨骼肌再生涉及不同细胞类型之间的协调相互作用。富含血小板的血浆注射被认为是肌肉修复的辅助手段,但血小板在止血之外是否能促进再生仍未得到探索。在这里,我们发现血小板释放的趋化因子信号是小鼠肌肉修复所必需的早期事件。血小板耗竭会降低血小板分泌的中性粒细胞趋化因子 CXCL5 和 CXCL7/PPBP 的水平。因此,早期中性粒细胞浸润受伤肌肉的能力受损,而后期炎症加剧。与该模型一致的是,血小板中缺失 Cxcl7 的雄性小鼠,其受伤肌肉的中性粒细胞浸润受损。此外,在受伤后,控制组小鼠的新血管生成和肌纤维大小及肌肉力量的重建最佳,但 Cxcl7ko 小鼠和中性粒细胞耗竭小鼠并非如此。总之,这些发现表明,血小板分泌的 CXCL7 通过募集中性粒细胞到受伤肌肉来促进再生,并且该信号轴可用于治疗以促进肌肉再生。