| Literature DB >> 28178531 |
Haibin Xi1, Wakana Fujiwara2, Karen Gonzalez3, Majib Jan4, Simone Liebscher5, Ben Van Handel6, Katja Schenke-Layland7, April D Pyle8.
Abstract
Somites form during embryonic development and give rise to unique cell and tissue types, such as skeletal muscles and bones and cartilage of the vertebrae. Using somitogenesis-stage human embryos, we performed transcriptomic profiling of human presomitic mesoderm as well as nascent and developed somites. In addition to conserved pathways such as WNT-β-catenin, we also identified BMP and transforming growth factor β (TGF-β) signaling as major regulators unique to human somitogenesis. This information enabled us to develop an efficient protocol to derive somite cells in vitro from human pluripotent stem cells (hPSCs). Importantly, the in-vitro-differentiating cells progressively expressed markers of the distinct developmental stages that are known to occur during in vivo somitogenesis. Furthermore, when subjected to lineage-specific differentiation conditions, the hPSC-derived somite cells were multipotent in generating somite derivatives, including skeletal myocytes, osteocytes, and chondrocytes. This work improves our understanding of human somitogenesis and may enhance our ability to treat diseases affecting somite derivatives. Published by Elsevier Inc.Entities:
Keywords: chondrogenesis; development; differentiation; human pluripotent stem cells; osteogenesis; skeletal myogenesis; somite
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Year: 2017 PMID: 28178531 PMCID: PMC5327729 DOI: 10.1016/j.celrep.2017.01.040
Source DB: PubMed Journal: Cell Rep Impact factor: 9.995