@article{517532c8b204487fb456972ae5661da9,
title = "Treatment of volumetric muscle loss in mice using nanofibrillar scaffolds enhances vascular organization and integration",
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.",
author = "Nakayama, {Karina H.} and Marco Quarta and Patrick Paine and Cynthia Alcazar and Ioannis Karakikes and Victor Garcia and Abilez, {Oscar J.} and Calvo, {Nicholas S.} and Simmons, {Chelsey S.} and Rando, {Thomas A.} and Huang, {Ngan F.}",
note = "Funding Information: We acknowledge Caroline Hu, Adam Davies, Igor Akimenko, and Zachary Strassberg for technical assistance with animal studies. In addition, we would like to thank Ramesh Nair and Gao Zhou for assisting with the RNA-Seq analysis. This research received funding from the Alliance for Regenerative Rehabilitation Research and Training (AR3T), which is supported by the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institute of Neurological Disorders and Stroke (NINDS), and National Institute of Biomedical Imaging and Bioengineering (NIBIB) of the National Institutes of Health under Award Number P2CHD086843. This study was supported by grants to N.F.H. from the US National Institutes of Health (R01 HL127113 and R01 HL142718), and the Department of Veterans Affairs (1I01BX002310 and 1I01BX004259). This work was also supported by grants from the National Institutes of Health (P01 AG036695), the California Institute of Regenerative Medicine, the Department of Defense, and the Department of Veterans Affairs (REAP and RR&D Merit Reviews) to T.A.R. K.H.N. was supported by a grant from the National Institutes of Health (K99 HL136701). Publisher Copyright: {\textcopyright} 2019, This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply.",
year = "2019",
month = dec,
day = "1",
doi = "10.1038/s42003-019-0416-4",
language = "English (US)",
volume = "2",
journal = "Communications Biology",
issn = "2399-3642",
publisher = "Springer Nature",
number = "1",
}