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Ectopic adipogenesis in response to injury and material implantation in an autoimmune mouse model

Due to the limited capacity of mammals to regenerate complex tissues, researchers have worked to understand the mechanisms of tissue regeneration in organisms that maintain that capacity. One example is the MRL/MpJ mouse strain with unique regenerative capacity in ear pinnae that is absent from othe...

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Autores principales: Ngo, Tran B., Josyula, Aditya, DeStefano, Sabrina, Fertil, Daphna, Faust, Mondreakest, Lokwani, Ravi, Sadtler, Kaitlyn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10659416/
https://www.ncbi.nlm.nih.gov/pubmed/37986843
http://dx.doi.org/10.1101/2023.10.05.561105
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author Ngo, Tran B.
Josyula, Aditya
DeStefano, Sabrina
Fertil, Daphna
Faust, Mondreakest
Lokwani, Ravi
Sadtler, Kaitlyn
author_facet Ngo, Tran B.
Josyula, Aditya
DeStefano, Sabrina
Fertil, Daphna
Faust, Mondreakest
Lokwani, Ravi
Sadtler, Kaitlyn
author_sort Ngo, Tran B.
collection PubMed
description Due to the limited capacity of mammals to regenerate complex tissues, researchers have worked to understand the mechanisms of tissue regeneration in organisms that maintain that capacity. One example is the MRL/MpJ mouse strain with unique regenerative capacity in ear pinnae that is absent from other strains, such as the common C57BL/6 strain. The MRL/MpJ mouse has also been associated with an autoimmune phenotype even in the absence of the mutant Fas gene described in its parent strain MRL/lpr. Due to these findings, we evaluated the differences between the responses of MRL/MpJ versus C57BL/6 strain in traumatic muscle injury and subsequent material implantation. One salient feature of the MRL/MpJ response to injury was a robust adipogenesis within the muscle. This was associated with a decrease in M2-like polarization in response to biologically derived extracellular matrix scaffolds. In pro-fibrotic materials, such as polyethylene, there were fewer foreign body giant cells in the MRL/MpJ mice. As there are reports of both positive and negative influences of adipose tissue and adipogenesis on wound healing, this model could provide an important lens to investigate the interplay between stem cells, adipose tissue, and immune responses in trauma and materials implantation.
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spelling pubmed-106594162023-11-20 Ectopic adipogenesis in response to injury and material implantation in an autoimmune mouse model Ngo, Tran B. Josyula, Aditya DeStefano, Sabrina Fertil, Daphna Faust, Mondreakest Lokwani, Ravi Sadtler, Kaitlyn bioRxiv Article Due to the limited capacity of mammals to regenerate complex tissues, researchers have worked to understand the mechanisms of tissue regeneration in organisms that maintain that capacity. One example is the MRL/MpJ mouse strain with unique regenerative capacity in ear pinnae that is absent from other strains, such as the common C57BL/6 strain. The MRL/MpJ mouse has also been associated with an autoimmune phenotype even in the absence of the mutant Fas gene described in its parent strain MRL/lpr. Due to these findings, we evaluated the differences between the responses of MRL/MpJ versus C57BL/6 strain in traumatic muscle injury and subsequent material implantation. One salient feature of the MRL/MpJ response to injury was a robust adipogenesis within the muscle. This was associated with a decrease in M2-like polarization in response to biologically derived extracellular matrix scaffolds. In pro-fibrotic materials, such as polyethylene, there were fewer foreign body giant cells in the MRL/MpJ mice. As there are reports of both positive and negative influences of adipose tissue and adipogenesis on wound healing, this model could provide an important lens to investigate the interplay between stem cells, adipose tissue, and immune responses in trauma and materials implantation. Cold Spring Harbor Laboratory 2023-10-07 /pmc/articles/PMC10659416/ /pubmed/37986843 http://dx.doi.org/10.1101/2023.10.05.561105 Text en https://creativecommons.org/publicdomain/zero/1.0/This article is a US Government work. It is not subject to copyright under 17 USC 105 and is also made available for use under a CC0 license (https://creativecommons.org/publicdomain/zero/1.0/) .
spellingShingle Article
Ngo, Tran B.
Josyula, Aditya
DeStefano, Sabrina
Fertil, Daphna
Faust, Mondreakest
Lokwani, Ravi
Sadtler, Kaitlyn
Ectopic adipogenesis in response to injury and material implantation in an autoimmune mouse model
title Ectopic adipogenesis in response to injury and material implantation in an autoimmune mouse model
title_full Ectopic adipogenesis in response to injury and material implantation in an autoimmune mouse model
title_fullStr Ectopic adipogenesis in response to injury and material implantation in an autoimmune mouse model
title_full_unstemmed Ectopic adipogenesis in response to injury and material implantation in an autoimmune mouse model
title_short Ectopic adipogenesis in response to injury and material implantation in an autoimmune mouse model
title_sort ectopic adipogenesis in response to injury and material implantation in an autoimmune mouse model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10659416/
https://www.ncbi.nlm.nih.gov/pubmed/37986843
http://dx.doi.org/10.1101/2023.10.05.561105
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