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Human muscle in gene edited pigs for treatment of volumetric muscle loss

Focusing on complex extremity trauma and volumetric muscle loss (VML) injuries, this review highlights: 1) the current pathophysiologic limitations of the injury sequela; 2) the gene editing strategy of the pig as a model that provides a novel treatment approach; 3) the notion that human skeletal mu...

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Autores principales: Greising, Sarah M., Weiner, Joshua I., Garry, Daniel J., Sachs, David H., Garry, Mary G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9358139/
https://www.ncbi.nlm.nih.gov/pubmed/35957684
http://dx.doi.org/10.3389/fgene.2022.948496
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author Greising, Sarah M.
Weiner, Joshua I.
Garry, Daniel J.
Sachs, David H.
Garry, Mary G.
author_facet Greising, Sarah M.
Weiner, Joshua I.
Garry, Daniel J.
Sachs, David H.
Garry, Mary G.
author_sort Greising, Sarah M.
collection PubMed
description Focusing on complex extremity trauma and volumetric muscle loss (VML) injuries, this review highlights: 1) the current pathophysiologic limitations of the injury sequela; 2) the gene editing strategy of the pig as a model that provides a novel treatment approach; 3) the notion that human skeletal muscle derived from gene edited, humanized pigs provides a groundbreaking treatment option; and 4) the impact of this technologic platform and how it will advance to far more multifaceted applications. This review seeks to shed insights on a novel treatment option using gene edited pigs as a platform which is necessary to overcome the clinical challenges and limitations in the field.
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spelling pubmed-93581392022-08-10 Human muscle in gene edited pigs for treatment of volumetric muscle loss Greising, Sarah M. Weiner, Joshua I. Garry, Daniel J. Sachs, David H. Garry, Mary G. Front Genet Genetics Focusing on complex extremity trauma and volumetric muscle loss (VML) injuries, this review highlights: 1) the current pathophysiologic limitations of the injury sequela; 2) the gene editing strategy of the pig as a model that provides a novel treatment approach; 3) the notion that human skeletal muscle derived from gene edited, humanized pigs provides a groundbreaking treatment option; and 4) the impact of this technologic platform and how it will advance to far more multifaceted applications. This review seeks to shed insights on a novel treatment option using gene edited pigs as a platform which is necessary to overcome the clinical challenges and limitations in the field. Frontiers Media S.A. 2022-07-25 /pmc/articles/PMC9358139/ /pubmed/35957684 http://dx.doi.org/10.3389/fgene.2022.948496 Text en Copyright © 2022 Greising, Weiner, Garry, Sachs and Garry. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Greising, Sarah M.
Weiner, Joshua I.
Garry, Daniel J.
Sachs, David H.
Garry, Mary G.
Human muscle in gene edited pigs for treatment of volumetric muscle loss
title Human muscle in gene edited pigs for treatment of volumetric muscle loss
title_full Human muscle in gene edited pigs for treatment of volumetric muscle loss
title_fullStr Human muscle in gene edited pigs for treatment of volumetric muscle loss
title_full_unstemmed Human muscle in gene edited pigs for treatment of volumetric muscle loss
title_short Human muscle in gene edited pigs for treatment of volumetric muscle loss
title_sort human muscle in gene edited pigs for treatment of volumetric muscle loss
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9358139/
https://www.ncbi.nlm.nih.gov/pubmed/35957684
http://dx.doi.org/10.3389/fgene.2022.948496
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