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Bioengineered constructs combined with exercise enhance stem cell-mediated treatment of volumetric muscle loss

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  • Marco Quarta

    (Stanford University School of Medicine
    Paul F. Glenn Laboratories for the Biology of Aging, Stanford University School of Medicine
    Center for Tissue Regeneration, Restoration and Repair, Veterans Affairs Hospital Palo Alto)

  • Melinda Cromie

    (Stanford University School of Medicine
    Paul F. Glenn Laboratories for the Biology of Aging, Stanford University School of Medicine
    Center for Tissue Regeneration, Restoration and Repair, Veterans Affairs Hospital Palo Alto)

  • Robert Chacon

    (Stanford University School of Medicine
    Paul F. Glenn Laboratories for the Biology of Aging, Stanford University School of Medicine
    Center for Tissue Regeneration, Restoration and Repair, Veterans Affairs Hospital Palo Alto)

  • Justin Blonigan

    (Stanford University School of Medicine
    Paul F. Glenn Laboratories for the Biology of Aging, Stanford University School of Medicine
    Center for Tissue Regeneration, Restoration and Repair, Veterans Affairs Hospital Palo Alto)

  • Victor Garcia

    (Stanford University School of Medicine
    Paul F. Glenn Laboratories for the Biology of Aging, Stanford University School of Medicine
    Center for Tissue Regeneration, Restoration and Repair, Veterans Affairs Hospital Palo Alto)

  • Igor Akimenko

    (Stanford University School of Medicine
    Paul F. Glenn Laboratories for the Biology of Aging, Stanford University School of Medicine
    Center for Tissue Regeneration, Restoration and Repair, Veterans Affairs Hospital Palo Alto)

  • Mark Hamer

    (Stanford University School of Medicine
    Paul F. Glenn Laboratories for the Biology of Aging, Stanford University School of Medicine
    Center for Tissue Regeneration, Restoration and Repair, Veterans Affairs Hospital Palo Alto)

  • Patrick Paine

    (Stanford University School of Medicine
    Paul F. Glenn Laboratories for the Biology of Aging, Stanford University School of Medicine
    Center for Tissue Regeneration, Restoration and Repair, Veterans Affairs Hospital Palo Alto)

  • Merel Stok

    (Erasmus Medical Center)

  • Joseph B. Shrager

    (Stanford University School of Medicine and VA Palo Alto Health Care System)

  • Thomas A. Rando

    (Stanford University School of Medicine
    Paul F. Glenn Laboratories for the Biology of Aging, Stanford University School of Medicine
    Center for Tissue Regeneration, Restoration and Repair, Veterans Affairs Hospital Palo Alto)

Abstract

Volumetric muscle loss (VML) is associated with loss of skeletal muscle function, and current treatments show limited efficacy. Here we show that bioconstructs suffused with genetically-labelled muscle stem cells (MuSCs) and other muscle resident cells (MRCs) are effective to treat VML injuries in mice. Imaging of bioconstructs implanted in damaged muscles indicates MuSCs survival and growth, and ex vivo analyses show force restoration of treated muscles. Histological analysis highlights myofibre formation, neovascularisation, but insufficient innervation. Both innervation and in vivo force production are enhanced when implantation of bioconstructs is followed by an exercise regimen. Significant improvements are also observed when bioconstructs are used to treat chronic VML injury models. Finally, we demonstrate that bioconstructs made with human MuSCs and MRCs can generate functional muscle tissue in our VML model. These data suggest that stem cell-based therapies aimed to engineer tissue in vivo may be effective to treat acute and chronic VML.

Suggested Citation

  • Marco Quarta & Melinda Cromie & Robert Chacon & Justin Blonigan & Victor Garcia & Igor Akimenko & Mark Hamer & Patrick Paine & Merel Stok & Joseph B. Shrager & Thomas A. Rando, 2017. "Bioengineered constructs combined with exercise enhance stem cell-mediated treatment of volumetric muscle loss," Nature Communications, Nature, vol. 8(1), pages 1-17, August.
  • Handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms15613
    DOI: 10.1038/ncomms15613
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