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Multiscale analysis of a regenerative therapy for treatment of volumetric muscle loss injury

Skeletal muscle possesses a remarkable capacity to regenerate when injured, but when confronted with major traumatic injury resulting in volumetric muscle loss (VML), the regenerative process consistently fails. The loss of muscle tissue and function from VML injury has prompted development of a sui...

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Autores principales: Aguilar, Carlos A., Greising, Sarah M., Watts, Alain, Goldman, Stephen M., Peragallo, Chelsea, Zook, Christina, Larouche, Jacqueline, Corona, Benjamin T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5841404/
https://www.ncbi.nlm.nih.gov/pubmed/29531830
http://dx.doi.org/10.1038/s41420-018-0027-8
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author Aguilar, Carlos A.
Greising, Sarah M.
Watts, Alain
Goldman, Stephen M.
Peragallo, Chelsea
Zook, Christina
Larouche, Jacqueline
Corona, Benjamin T.
author_facet Aguilar, Carlos A.
Greising, Sarah M.
Watts, Alain
Goldman, Stephen M.
Peragallo, Chelsea
Zook, Christina
Larouche, Jacqueline
Corona, Benjamin T.
author_sort Aguilar, Carlos A.
collection PubMed
description Skeletal muscle possesses a remarkable capacity to regenerate when injured, but when confronted with major traumatic injury resulting in volumetric muscle loss (VML), the regenerative process consistently fails. The loss of muscle tissue and function from VML injury has prompted development of a suite of therapeutic approaches but these strategies have proceeded without a comprehensive understanding of the molecular landscape that drives the injury response. Herein, we administered a VML injury in an established rodent model and monitored the evolution of the healing phenomenology over multiple time points using muscle function testing, histology, and expression profiling by RNA sequencing. The injury response was then compared to a regenerative medicine treatment using orthotopic transplantation of autologous minced muscle grafts (~1 mm(3) tissue fragments). A chronic inflammatory and fibrotic response was observed at all time points following VML. These results suggest that the pathological response to VML injury during the acute stage of the healing response overwhelms endogenous and therapeutic regenerative processes. Overall, the data presented delineate key molecular characteristics of the pathobiological response to VML injury that are critical effectors of effective regenerative treatment paradigms.
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spelling pubmed-58414042018-03-12 Multiscale analysis of a regenerative therapy for treatment of volumetric muscle loss injury Aguilar, Carlos A. Greising, Sarah M. Watts, Alain Goldman, Stephen M. Peragallo, Chelsea Zook, Christina Larouche, Jacqueline Corona, Benjamin T. Cell Death Discov Article Skeletal muscle possesses a remarkable capacity to regenerate when injured, but when confronted with major traumatic injury resulting in volumetric muscle loss (VML), the regenerative process consistently fails. The loss of muscle tissue and function from VML injury has prompted development of a suite of therapeutic approaches but these strategies have proceeded without a comprehensive understanding of the molecular landscape that drives the injury response. Herein, we administered a VML injury in an established rodent model and monitored the evolution of the healing phenomenology over multiple time points using muscle function testing, histology, and expression profiling by RNA sequencing. The injury response was then compared to a regenerative medicine treatment using orthotopic transplantation of autologous minced muscle grafts (~1 mm(3) tissue fragments). A chronic inflammatory and fibrotic response was observed at all time points following VML. These results suggest that the pathological response to VML injury during the acute stage of the healing response overwhelms endogenous and therapeutic regenerative processes. Overall, the data presented delineate key molecular characteristics of the pathobiological response to VML injury that are critical effectors of effective regenerative treatment paradigms. Nature Publishing Group UK 2018-02-20 /pmc/articles/PMC5841404/ /pubmed/29531830 http://dx.doi.org/10.1038/s41420-018-0027-8 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Aguilar, Carlos A.
Greising, Sarah M.
Watts, Alain
Goldman, Stephen M.
Peragallo, Chelsea
Zook, Christina
Larouche, Jacqueline
Corona, Benjamin T.
Multiscale analysis of a regenerative therapy for treatment of volumetric muscle loss injury
title Multiscale analysis of a regenerative therapy for treatment of volumetric muscle loss injury
title_full Multiscale analysis of a regenerative therapy for treatment of volumetric muscle loss injury
title_fullStr Multiscale analysis of a regenerative therapy for treatment of volumetric muscle loss injury
title_full_unstemmed Multiscale analysis of a regenerative therapy for treatment of volumetric muscle loss injury
title_short Multiscale analysis of a regenerative therapy for treatment of volumetric muscle loss injury
title_sort multiscale analysis of a regenerative therapy for treatment of volumetric muscle loss injury
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5841404/
https://www.ncbi.nlm.nih.gov/pubmed/29531830
http://dx.doi.org/10.1038/s41420-018-0027-8
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