Department of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, CA, USA; Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, University of California, Los Angeles, Los Angeles, CA, USA.
Deparment of Biological Chemistry, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, USA.
Cell Stem Cell. 2020 Jul 2;27(1):158-176.e10. doi: 10.1016/j.stem.2020.04.017. Epub 2020 May 11.
The developmental trajectory of human skeletal myogenesis and the transition between progenitor and stem cell states are unclear. We used single-cell RNA sequencing to profile human skeletal muscle tissues from embryonic, fetal, and postnatal stages. In silico, we identified myogenic as well as other cell types and constructed a "roadmap" of human skeletal muscle ontogeny across development. In a similar fashion, we also profiled the heterogeneous cell cultures generated from multiple human pluripotent stem cell (hPSC) myogenic differentiation protocols and mapped hPSC-derived myogenic progenitors to an embryonic-to-fetal transition period. We found differentially enriched biological processes and discovered co-regulated gene networks and transcription factors present at distinct myogenic stages. This work serves as a resource for advancing our knowledge of human myogenesis. It also provides a tool for a better understanding of hPSC-derived myogenic progenitors for translational applications in skeletal muscle-based regenerative medicine.
人类骨骼肌发生的发展轨迹和祖细胞与干细胞状态之间的转变尚不清楚。我们使用单细胞 RNA 测序技术对胚胎期、胎儿期和出生后阶段的人类骨骼肌组织进行了分析。通过计算机模拟,我们鉴定出了成肌细胞以及其他细胞类型,并构建了一个贯穿发育过程的人类骨骼肌发生的“路线图”。以类似的方式,我们还对来自多种人类多能干细胞 (hPSC) 成肌分化方案的异质细胞培养物进行了分析,并将 hPSC 衍生的成肌祖细胞映射到胚胎到胎儿的过渡时期。我们发现了差异丰富的生物学过程,并发现了在不同成肌阶段存在的共同调控的基因网络和转录因子。这项工作为我们深入了解人类成肌发生提供了资源。它还为更好地理解 hPSC 衍生的成肌祖细胞提供了工具,可用于基于骨骼肌的再生医学的转化应用。