Treatment of volumetric muscle loss in mice using nanofibrillar scaffolds enhances vascular organization and integration

Commun Biol. 2019 May 7:2:170. doi: 10.1038/s42003-019-0416-4. eCollection 2019.

Abstract

Traumatic skeletal muscle injuries cause irreversible tissue damage and impaired revascularization. Engineered muscle is promising for enhancing tissue revascularization and regeneration in injured muscle. Here we fabricated engineered skeletal muscle composed of myotubes interspersed with vascular endothelial cells using spatially patterned scaffolds that induce aligned cellular organization, and then assessed their therapeutic benefit for treatment of murine volumetric muscle loss. Murine skeletal myoblasts co-cultured with endothelial cells in aligned nanofibrillar scaffolds form endothelialized and aligned muscle with longer myotubes, more synchronized contractility, and more abundant secretion of angiogenic cytokines, compared to endothelialized engineered muscle formed from randomly-oriented scaffolds. Treatment of traumatically injured muscle with endothelialized and aligned skeletal muscle promotes the formation of highly organized myofibers and microvasculature, along with greater vascular perfusion, compared to treatment of muscle derived from randomly-oriented scaffolds. This work demonstrates the potential of endothelialized and aligned engineered skeletal muscle to promote vascular regeneration following transplantation.

Keywords: Cell therapies; Musculoskeletal models; Regeneration; Tissue engineering; Tissues.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Cell Line
  • Coculture Techniques
  • Cytokines / biosynthesis
  • Endothelial Cells / cytology
  • Endothelial Cells / physiology
  • Humans
  • Mice
  • Muscle Fibers, Skeletal / physiology
  • Muscle, Skeletal / blood supply*
  • Muscle, Skeletal / injuries*
  • Muscle, Skeletal / physiology
  • Myoblasts, Skeletal / cytology
  • Nanofibers / ultrastructure
  • Regeneration / physiology
  • Tissue Engineering / methods*
  • Tissue Scaffolds

Substances

  • Cytokines