| Literature DB >> 35395188 |
Congshan Sun1, Suraj Kannan2, In Young Choi3, HoTae Lim3, Hao Zhang4, Grace S Chen5, Nancy Zhang5, Seong-Hyun Park3, Carlo Serra1, Shama R Iyer6, Thomas E Lloyd7, Chulan Kwon2, Richard M Lovering6, Su Bin Lim8, Peter Andersen9, Kathryn R Wagner10, Gabsang Lee11.
Abstract
Human pluripotent stem cell (hPSC)-derived myogenic progenitor cell (MPC) transplantation is a promising therapeutic approach for a variety of degenerative muscle disorders. Here, using an MPC-specific fluorescent reporter system (PAX7::GFP), we demonstrate that hPSC-derived MPCs can contribute to the regeneration of myofibers in mice following local injury and in mice deficient of dystrophin (mdx). We also demonstrate that a subset of PAX7::GFP MPCs engraft within the basal lamina of regenerated myofibers, adopt a quiescent state, and contribute to regeneration upon reinjury and in mdx mouse models. This subset of PAX7::GFP MPCs undergo a maturation process and remodel their molecular characteristics to resemble those of late-stage fetal MPCs/adult satellite cells following in vivo engraftment. These in-vivo-matured PAX7::GFP MPCs retain a cell-autonomous ability to regenerate and can repopulate in the niche of secondary recipient mice, providing a proof of principle for future hPSC-based cell therapy for muscle disorders.Entities:
Keywords: Duchenne muscular dystrophy; mdx mouse; pluripotent stem cells; quiescent stem cells; skeletal muscle stem cells
Mesh:
Substances:
Year: 2022 PMID: 35395188 PMCID: PMC9000524 DOI: 10.1016/j.stem.2022.03.004
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 25.269