4.3 Article

Engineering Skeletal Muscle Grafts with PAX7::GFP-Sorted Human Pluripotent Stem Cell-Derived Myogenic Progenitors on Fibrin Microfiber Bundles for Tissue Regeneration

期刊

BIOENGINEERING-BASEL
卷 9, 期 11, 页码 -

出版社

MDPI
DOI: 10.3390/bioengineering9110693

关键词

human pluripotent stem cells (hPSCs); hPSC-derived myogenic progenitors (hPDMs) PAX7; skeletal muscle tissue engineering; skeletal muscle injury and regeneration; fibrin microfiber bundles

资金

  1. Maryland Stem Cell Research Fund [2016-MSCRFI-2692]
  2. Wilmer Core Grant for Vision Research [EY001765]
  3. Microscopy and Imaging Core Module
  4. NIH [1R01AR077581]
  5. NIAMS

向作者/读者索取更多资源

Tissue engineering strategies combining human pluripotent stem cells and advanced biomaterials can be used to engineer skeletal muscle grafts, providing a model for tissue development and promoting muscle regeneration. In this study, the researchers demonstrated the formation of engineered human skeletal muscle grafts containing multinucleated myotubes using fibrin microfiber bundles and PAX7::GFP-sorted hPDMs, which showed potential for promoting in vivo skeletal muscle regeneration.
Tissue engineering strategies that combine human pluripotent stem cell-derived myogenic progenitors (hPDMs) with advanced biomaterials provide promising tools for engineering 3D skeletal muscle grafts to model tissue development in vitro and promote muscle regeneration in vivo. We recently demonstrated (i) the potential for obtaining large numbers of hPDMs using a combination of two small molecules without the overexpression of transgenes and (ii) the application of electrospun fibrin microfiber bundles for functional skeletal muscle restoration following volumetric muscle loss. In this study, we aimed to demonstrate that the biophysical cues provided by the fibrin microfiber bundles induce hPDMs to form engineered human skeletal muscle grafts containing multinucleated myotubes that express desmin and myosin heavy chains and that these grafts could promote regeneration following skeletal muscle injuries. We tested a genetic PAX7 reporter line (PAX7::GFP) to sort for more homogenous populations of hPDMs. RNA sequencing and gene set enrichment analyses confirmed that PAX7::GFP-sorted hPDMs exhibited high expression of myogenic genes. We tested engineered human skeletal muscle grafts derived from PAX7::GFP-sorted hPDMs within in vivo skeletal muscle defects by assessing myogenesis, engraftment and immunogenicity using immunohistochemical staining. The PAX7::GFP-sorted groups had moderately high vascular infiltration and more implanted cell association with embryonic myosin heavy chain (eMHC) regions, suggesting they induced pro-regenerative microenvironments. These findings demonstrated the promise for the use of PAX7::GFP-sorted hPDMs on fibrin microfiber bundles and provided some insights for improving the cell-biomaterial system to stimulate more robust in vivo skeletal muscle regeneration.

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