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Effects of intraperitoneal injection of microencapsulated Sertoli cells on chronic and presymptomatic dystrophic mice
We report data about the effects of intraperitoneal (i.p.) injection of specific pathogen-free (SPF) porcine Sertoli cells (SeC) encapsulated into clinical grade alginate-based microcapsules (SeC-MC) on muscles of chronic and presymptomatic dystrophic, mdx mice. Mdx mouse is the best characterized a...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683552/ https://www.ncbi.nlm.nih.gov/pubmed/26759818 http://dx.doi.org/10.1016/j.dib.2015.11.016 |
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author | Chiappalupi, Sara Luca, Giovanni Mancuso, Francesca Madaro, Luca Fallarino, Francesca Nicoletti, Carmine Calvitti, Mario Arato, Iva Falabella, Giulia Salvadori, Laura Di Meo, Antonio Bufalari, Antonello Giovagnoli, Stefano Calafiore, Riccardo Donato, Rosario Sorci, Guglielmo |
author_facet | Chiappalupi, Sara Luca, Giovanni Mancuso, Francesca Madaro, Luca Fallarino, Francesca Nicoletti, Carmine Calvitti, Mario Arato, Iva Falabella, Giulia Salvadori, Laura Di Meo, Antonio Bufalari, Antonello Giovagnoli, Stefano Calafiore, Riccardo Donato, Rosario Sorci, Guglielmo |
author_sort | Chiappalupi, Sara |
collection | PubMed |
description | We report data about the effects of intraperitoneal (i.p.) injection of specific pathogen-free (SPF) porcine Sertoli cells (SeC) encapsulated into clinical grade alginate-based microcapsules (SeC-MC) on muscles of chronic and presymptomatic dystrophic, mdx mice. Mdx mouse is the best characterized animal model of Duchenne muscular dystrophy (DMD), an X-linked lethal myopathy due to mutation in the gene of dystrophin, which is crucial for myofiber integrity during muscle contraction. Our data show that three weeks after i.p. injection of SeC-MC significantly reduced adipose and fibrous tissue deposition, reduced macrophage infiltrate, and reduced numbers of damaged myofibers are found in muscles of 12-month-old mdx mice, which reproduce chronic DMD conditions. Compared with muscles of mock-treated mdx mice muscles of SeC-MC-treated mice show upregulation of the dystrophin paralogue, utrophin which is localized to the periphery of myofibers. Moreover, our data show that i.p. injection of SeC-MC into presymptomatic, 2-week-old mdx mice, although not fully preventing myofiber degeneration, results in protection against myofiber necrosis and muscle inflammation. Extensive discussion of these data can be found in Ref. [1]. |
format | Online Article Text |
id | pubmed-4683552 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-46835522016-01-12 Effects of intraperitoneal injection of microencapsulated Sertoli cells on chronic and presymptomatic dystrophic mice Chiappalupi, Sara Luca, Giovanni Mancuso, Francesca Madaro, Luca Fallarino, Francesca Nicoletti, Carmine Calvitti, Mario Arato, Iva Falabella, Giulia Salvadori, Laura Di Meo, Antonio Bufalari, Antonello Giovagnoli, Stefano Calafiore, Riccardo Donato, Rosario Sorci, Guglielmo Data Brief Data Article We report data about the effects of intraperitoneal (i.p.) injection of specific pathogen-free (SPF) porcine Sertoli cells (SeC) encapsulated into clinical grade alginate-based microcapsules (SeC-MC) on muscles of chronic and presymptomatic dystrophic, mdx mice. Mdx mouse is the best characterized animal model of Duchenne muscular dystrophy (DMD), an X-linked lethal myopathy due to mutation in the gene of dystrophin, which is crucial for myofiber integrity during muscle contraction. Our data show that three weeks after i.p. injection of SeC-MC significantly reduced adipose and fibrous tissue deposition, reduced macrophage infiltrate, and reduced numbers of damaged myofibers are found in muscles of 12-month-old mdx mice, which reproduce chronic DMD conditions. Compared with muscles of mock-treated mdx mice muscles of SeC-MC-treated mice show upregulation of the dystrophin paralogue, utrophin which is localized to the periphery of myofibers. Moreover, our data show that i.p. injection of SeC-MC into presymptomatic, 2-week-old mdx mice, although not fully preventing myofiber degeneration, results in protection against myofiber necrosis and muscle inflammation. Extensive discussion of these data can be found in Ref. [1]. Elsevier 2015-11-15 /pmc/articles/PMC4683552/ /pubmed/26759818 http://dx.doi.org/10.1016/j.dib.2015.11.016 Text en © 2015 Published by Elsevier Inc. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Data Article Chiappalupi, Sara Luca, Giovanni Mancuso, Francesca Madaro, Luca Fallarino, Francesca Nicoletti, Carmine Calvitti, Mario Arato, Iva Falabella, Giulia Salvadori, Laura Di Meo, Antonio Bufalari, Antonello Giovagnoli, Stefano Calafiore, Riccardo Donato, Rosario Sorci, Guglielmo Effects of intraperitoneal injection of microencapsulated Sertoli cells on chronic and presymptomatic dystrophic mice |
title | Effects of intraperitoneal injection of microencapsulated Sertoli cells on chronic and presymptomatic dystrophic mice |
title_full | Effects of intraperitoneal injection of microencapsulated Sertoli cells on chronic and presymptomatic dystrophic mice |
title_fullStr | Effects of intraperitoneal injection of microencapsulated Sertoli cells on chronic and presymptomatic dystrophic mice |
title_full_unstemmed | Effects of intraperitoneal injection of microencapsulated Sertoli cells on chronic and presymptomatic dystrophic mice |
title_short | Effects of intraperitoneal injection of microencapsulated Sertoli cells on chronic and presymptomatic dystrophic mice |
title_sort | effects of intraperitoneal injection of microencapsulated sertoli cells on chronic and presymptomatic dystrophic mice |
topic | Data Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683552/ https://www.ncbi.nlm.nih.gov/pubmed/26759818 http://dx.doi.org/10.1016/j.dib.2015.11.016 |
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