Camargo Fernando D, Green Rahshaana, Capetanaki Yassemi, Jackson Kathyjo A, Goodell Margaret A
Center for Cell and Gene Therapy, Baylor College of Medicine, One Baylor Plaza, BCM505, Houston, Texas 77030, USA.
Nat Med. 2003 Dec;9(12):1520-7. doi: 10.1038/nm963. Epub 2003 Nov 16.
Recent studies have shown that cells from the bone marrow can give rise to differentiated skeletal muscle fibers. However, the mechanisms and identities of the cell types involved have remained unknown, and the validity of the observation has been questioned. Here, we use transplantation of single CD45+ hematopoietic stem cells (HSCs) to demonstrate that the entire circulating myogenic activity in bone marrow is derived from HSCs and their hematopoietic progeny. We also show that ongoing muscle regeneration and inflammatory cell infiltration are required for HSC-derived contribution, which does not occur through a myogenic stem cell intermediate. Using a lineage tracing strategy, we show that myofibers are derived from mature myeloid cells in response to injury. Our results indicate that circulating myeloid cells, in response to inflammatory cues, migrate to regenerating skeletal muscle and stochastically incorporate into mature myofibers.
最近的研究表明,骨髓细胞可分化形成骨骼肌纤维。然而,其中涉及的细胞类型和机制尚不清楚,这一观察结果的有效性也受到了质疑。在此,我们通过移植单个CD45+造血干细胞(HSCs)来证明,骨髓中所有循环的生肌活性均源自造血干细胞及其造血后代。我们还表明,造血干细胞衍生的贡献需要持续的肌肉再生和炎性细胞浸润,且并非通过生肌干细胞中间体发生。利用谱系追踪策略,我们发现肌纤维源自成熟髓细胞对损伤的反应。我们的结果表明,循环髓细胞在炎症信号的作用下迁移至再生的骨骼肌,并随机整合到成熟肌纤维中。