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Progression of inflammation during immunodeficient mouse skeletal muscle regeneration
The skeletal muscle injury triggers the inflammatory response which is crucial for damaged muscle fiber degradation and satellite cell activation. Immunodeficient mice are often used as a model to study the myogenic potential of transplanted human stem cells. Therefore, it is crucial to elucidate wh...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4762921/ https://www.ncbi.nlm.nih.gov/pubmed/26613733 http://dx.doi.org/10.1007/s10974-015-9433-1 |
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author | Grabowska, Iwona Mazur, Magdalena A. Kowalski, K. Helinska, A. Moraczewski, Jerzy Stremińska, Władysława Hoser, Grażyna Kawiak, Jerzy Ciemerych, Maria A. Brzoska, Edyta |
author_facet | Grabowska, Iwona Mazur, Magdalena A. Kowalski, K. Helinska, A. Moraczewski, Jerzy Stremińska, Władysława Hoser, Grażyna Kawiak, Jerzy Ciemerych, Maria A. Brzoska, Edyta |
author_sort | Grabowska, Iwona |
collection | PubMed |
description | The skeletal muscle injury triggers the inflammatory response which is crucial for damaged muscle fiber degradation and satellite cell activation. Immunodeficient mice are often used as a model to study the myogenic potential of transplanted human stem cells. Therefore, it is crucial to elucidate whether such model truly reflects processes occurring under physiological conditions. To answer this question we compared skeletal muscle regeneration of BALB/c, i.e. animals producing all types of inflammatory cells, and SCID mice. Results of our study documented that initial stages of muscles regeneration in both strains of mice were comparable. However, lower number of mononucleated cells was noticed in regenerating SCID mouse muscles. Significant differences in the number of CD14-/CD45+ and CD14+/CD45+ cells between BALB/c and SCID muscles were also observed. In addition, we found important differences in M1 and M2 macrophage levels of BALB/c and SCID mouse muscles identified by CD68 and CD163 markers. Thus, our data show that differences in inflammatory response during muscle regeneration, were not translated into significant modifications in muscle regeneration. |
format | Online Article Text |
id | pubmed-4762921 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-47629212016-03-03 Progression of inflammation during immunodeficient mouse skeletal muscle regeneration Grabowska, Iwona Mazur, Magdalena A. Kowalski, K. Helinska, A. Moraczewski, Jerzy Stremińska, Władysława Hoser, Grażyna Kawiak, Jerzy Ciemerych, Maria A. Brzoska, Edyta J Muscle Res Cell Motil Original Paper The skeletal muscle injury triggers the inflammatory response which is crucial for damaged muscle fiber degradation and satellite cell activation. Immunodeficient mice are often used as a model to study the myogenic potential of transplanted human stem cells. Therefore, it is crucial to elucidate whether such model truly reflects processes occurring under physiological conditions. To answer this question we compared skeletal muscle regeneration of BALB/c, i.e. animals producing all types of inflammatory cells, and SCID mice. Results of our study documented that initial stages of muscles regeneration in both strains of mice were comparable. However, lower number of mononucleated cells was noticed in regenerating SCID mouse muscles. Significant differences in the number of CD14-/CD45+ and CD14+/CD45+ cells between BALB/c and SCID muscles were also observed. In addition, we found important differences in M1 and M2 macrophage levels of BALB/c and SCID mouse muscles identified by CD68 and CD163 markers. Thus, our data show that differences in inflammatory response during muscle regeneration, were not translated into significant modifications in muscle regeneration. Springer International Publishing 2015-11-27 2015 /pmc/articles/PMC4762921/ /pubmed/26613733 http://dx.doi.org/10.1007/s10974-015-9433-1 Text en © The Author(s) 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Original Paper Grabowska, Iwona Mazur, Magdalena A. Kowalski, K. Helinska, A. Moraczewski, Jerzy Stremińska, Władysława Hoser, Grażyna Kawiak, Jerzy Ciemerych, Maria A. Brzoska, Edyta Progression of inflammation during immunodeficient mouse skeletal muscle regeneration |
title | Progression of inflammation during immunodeficient mouse skeletal muscle regeneration |
title_full | Progression of inflammation during immunodeficient mouse skeletal muscle regeneration |
title_fullStr | Progression of inflammation during immunodeficient mouse skeletal muscle regeneration |
title_full_unstemmed | Progression of inflammation during immunodeficient mouse skeletal muscle regeneration |
title_short | Progression of inflammation during immunodeficient mouse skeletal muscle regeneration |
title_sort | progression of inflammation during immunodeficient mouse skeletal muscle regeneration |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4762921/ https://www.ncbi.nlm.nih.gov/pubmed/26613733 http://dx.doi.org/10.1007/s10974-015-9433-1 |
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