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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
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].
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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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