4.7 Article

Pre-innervated tissue-engineered muscle promotes a pro-regenerative microenvironment following volumetric muscle loss

Journal

COMMUNICATIONS BIOLOGY
Volume 3, Issue 1, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s42003-020-1056-4

Keywords

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Funding

  1. U.S. Department of Defense through the Medical Research and Materiel Command [W81XWH-19-1-0867, W81XWH-16-1-0796, W81XWH-15-1-0466]
  2. National Institutes of Health [BRAIN Initiative] [U01-NS094340]
  3. Department of Veterans Affairs [I01-BX003748]

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Volumetric muscle loss (VML) is the traumatic or surgical loss of skeletal muscle beyond the inherent regenerative capacity of the body, generally leading to severe functional deficit. Formation of appropriate somato-motor innervations remains one of the biggest challenges for both autologous grafts as well as tissue-engineered muscle constructs. We aim to address this challenge by developing pre-innervated tissue-engineered muscle comprised of long aligned networks of spinal motor neurons and skeletal myocytes on aligned nanofibrous scaffolds. Motor neurons led to enhanced differentiation and maturation of skeletal myocytes in vitro. These pre-innervated tissue-engineered muscle constructs when implanted in a rat VML model significantly increased satellite cell density, neuromuscular junction maintenance, graft revascularization, and muscle volume over three weeks as compared to myocyte-only constructs and nanofiber scaffolds alone. These pro-regenerative effects may enhance functional neuromuscular regeneration following VML, thereby improving the levels of functional recovery following these devastating injuries. Das et al. create a bioengineered construct combining nerve and muscle cells on a biomimetic scaffold to improve recovery from volumetric muscle loss (VML). When implanted into a rat VML model, they report an increase in in vitro parameters of muscle fiber development and formation of neuromuscular junctions, which support in vivo observations of improved implanted cell survival and vascularization.

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