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Do porcine Sertoli cells represent an opportunity for Duchenne muscular dystrophy?
Sertoli cells (SeC) are responsible for the immunoprivileged status of the testis thanks to which allogeneic or xenogeneic engraftments can survive without pharmacological immune suppression if co‐injected with SeC. This peculiar ability of SeC is dependent on secretion of a plethora of factors incl...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536415/ https://www.ncbi.nlm.nih.gov/pubmed/30912260 http://dx.doi.org/10.1111/cpr.12599 |
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author | Chiappalupi, Sara Salvadori, Laura Luca, Giovanni Riuzzi, Francesca Calafiore, Riccardo Donato, Rosario Sorci, Guglielmo |
author_facet | Chiappalupi, Sara Salvadori, Laura Luca, Giovanni Riuzzi, Francesca Calafiore, Riccardo Donato, Rosario Sorci, Guglielmo |
author_sort | Chiappalupi, Sara |
collection | PubMed |
description | Sertoli cells (SeC) are responsible for the immunoprivileged status of the testis thanks to which allogeneic or xenogeneic engraftments can survive without pharmacological immune suppression if co‐injected with SeC. This peculiar ability of SeC is dependent on secretion of a plethora of factors including maturation factors, hormones, growth factors, cytokines and immunomodulatory factors. The anti‐inflammatory and trophic properties of SeC have been largely exploited in several experimental models of diseases, diabetes being the most studied. Duchenne muscular dystrophy (DMD) is a lethal X‐linked recessive pathology in which lack of functional dystrophin leads to progressive muscle degeneration culminating in loss of locomotion and premature death. Despite a huge effort to find a cure, DMD patients are currently treated with anti‐inflammatory steroids. Recently, encapsulated porcine SeC (MC‐SeC) have been injected ip in the absence of immunosuppression in an animal model of DMD resulting in reduction of muscle inflammation and amelioration of muscle morphology and functionality, thus opening an additional avenue in the treatment of DMD. The novel protocol is endowed with the advantage of being potentially applicable to all the cohort of DMD patients regardless of the mutation. This mini‐review addresses several issues linked to the possible use of MC‐SeC injected ip in dystrophic people. |
format | Online Article Text |
id | pubmed-6536415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65364152020-03-13 Do porcine Sertoli cells represent an opportunity for Duchenne muscular dystrophy? Chiappalupi, Sara Salvadori, Laura Luca, Giovanni Riuzzi, Francesca Calafiore, Riccardo Donato, Rosario Sorci, Guglielmo Cell Prolif Review Sertoli cells (SeC) are responsible for the immunoprivileged status of the testis thanks to which allogeneic or xenogeneic engraftments can survive without pharmacological immune suppression if co‐injected with SeC. This peculiar ability of SeC is dependent on secretion of a plethora of factors including maturation factors, hormones, growth factors, cytokines and immunomodulatory factors. The anti‐inflammatory and trophic properties of SeC have been largely exploited in several experimental models of diseases, diabetes being the most studied. Duchenne muscular dystrophy (DMD) is a lethal X‐linked recessive pathology in which lack of functional dystrophin leads to progressive muscle degeneration culminating in loss of locomotion and premature death. Despite a huge effort to find a cure, DMD patients are currently treated with anti‐inflammatory steroids. Recently, encapsulated porcine SeC (MC‐SeC) have been injected ip in the absence of immunosuppression in an animal model of DMD resulting in reduction of muscle inflammation and amelioration of muscle morphology and functionality, thus opening an additional avenue in the treatment of DMD. The novel protocol is endowed with the advantage of being potentially applicable to all the cohort of DMD patients regardless of the mutation. This mini‐review addresses several issues linked to the possible use of MC‐SeC injected ip in dystrophic people. John Wiley and Sons Inc. 2019-03-26 /pmc/articles/PMC6536415/ /pubmed/30912260 http://dx.doi.org/10.1111/cpr.12599 Text en © 2019 The Authors. Cell Proliferation Published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Chiappalupi, Sara Salvadori, Laura Luca, Giovanni Riuzzi, Francesca Calafiore, Riccardo Donato, Rosario Sorci, Guglielmo Do porcine Sertoli cells represent an opportunity for Duchenne muscular dystrophy? |
title | Do porcine Sertoli cells represent an opportunity for Duchenne muscular dystrophy? |
title_full | Do porcine Sertoli cells represent an opportunity for Duchenne muscular dystrophy? |
title_fullStr | Do porcine Sertoli cells represent an opportunity for Duchenne muscular dystrophy? |
title_full_unstemmed | Do porcine Sertoli cells represent an opportunity for Duchenne muscular dystrophy? |
title_short | Do porcine Sertoli cells represent an opportunity for Duchenne muscular dystrophy? |
title_sort | do porcine sertoli cells represent an opportunity for duchenne muscular dystrophy? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536415/ https://www.ncbi.nlm.nih.gov/pubmed/30912260 http://dx.doi.org/10.1111/cpr.12599 |
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