| Literature DB >> 32396864 |
Haibin Xi1, Justin Langerman2, Shan Sabri2, Peggie Chien3, Courtney S Young4, Shahab Younesi1, Michael Hicks1, Karen Gonzalez5, Wakana Fujiwara6, Julia Marzi7, Simone Liebscher8, Melissa Spencer9, Ben Van Handel10, Denis Evseenko10, Katja Schenke-Layland11, Kathrin Plath12, April D Pyle13.
Abstract
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. Published by Elsevier Inc.Entities:
Keywords: development; human myogenesis; pluripotent stem cells; satellite cells; single cell RNA-sequencing; skeletal muscle
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Year: 2020 PMID: 32396864 PMCID: PMC7367475 DOI: 10.1016/j.stem.2020.04.017
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 25.269