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Conditional Cripto overexpression in satellite cells promotes myogenic commitment and enhances early regeneration

Skeletal muscle regeneration mainly depends on satellite cells, a population of resident muscle stem cells. Despite extensive studies, knowledge of the molecular mechanisms underlying the early events associated with satellite cell activation and myogenic commitment in muscle regeneration remains st...

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Autores principales: Prezioso, Carolina, Iaconis, Salvatore, Andolfi, Gennaro, Zentilin, Lorena, Iavarone, Francescopaolo, Guardiola, Ombretta, Minchiotti, Gabriella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439575/
https://www.ncbi.nlm.nih.gov/pubmed/26052513
http://dx.doi.org/10.3389/fcell.2015.00031
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author Prezioso, Carolina
Iaconis, Salvatore
Andolfi, Gennaro
Zentilin, Lorena
Iavarone, Francescopaolo
Guardiola, Ombretta
Minchiotti, Gabriella
author_facet Prezioso, Carolina
Iaconis, Salvatore
Andolfi, Gennaro
Zentilin, Lorena
Iavarone, Francescopaolo
Guardiola, Ombretta
Minchiotti, Gabriella
author_sort Prezioso, Carolina
collection PubMed
description Skeletal muscle regeneration mainly depends on satellite cells, a population of resident muscle stem cells. Despite extensive studies, knowledge of the molecular mechanisms underlying the early events associated with satellite cell activation and myogenic commitment in muscle regeneration remains still incomplete. Cripto is a novel regulator of postnatal skeletal muscle regeneration and a promising target for future therapy. Indeed, Cripto is expressed both in myogenic and inflammatory cells in skeletal muscle after acute injury and it is required in the satellite cell compartment to achieve effective muscle regeneration. A critical requirement to further explore the in vivo cellular contribution of Cripto in regulating skeletal muscle regeneration is the possibility to overexpress Cripto in its endogenous configuration and in a cell and time-specific manner. Here we report the generation and the functional characterization of a novel mouse model for conditional expression of Cripto, i.e., the Tg:DsRed(loxP/loxP)Cripto-eGFP mice. Moreover, by using a satellite cell specific Cre-driver line we investigated the biological effect of Cripto overexpression in vivo, and provided evidence that overexpression of Cripto in the adult satellite cell compartment promotes myogenic commitment and differentiation, and enhances early regeneration in a mouse model of acute injury.
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spelling pubmed-44395752015-06-05 Conditional Cripto overexpression in satellite cells promotes myogenic commitment and enhances early regeneration Prezioso, Carolina Iaconis, Salvatore Andolfi, Gennaro Zentilin, Lorena Iavarone, Francescopaolo Guardiola, Ombretta Minchiotti, Gabriella Front Cell Dev Biol Cell and Developmental Biology Skeletal muscle regeneration mainly depends on satellite cells, a population of resident muscle stem cells. Despite extensive studies, knowledge of the molecular mechanisms underlying the early events associated with satellite cell activation and myogenic commitment in muscle regeneration remains still incomplete. Cripto is a novel regulator of postnatal skeletal muscle regeneration and a promising target for future therapy. Indeed, Cripto is expressed both in myogenic and inflammatory cells in skeletal muscle after acute injury and it is required in the satellite cell compartment to achieve effective muscle regeneration. A critical requirement to further explore the in vivo cellular contribution of Cripto in regulating skeletal muscle regeneration is the possibility to overexpress Cripto in its endogenous configuration and in a cell and time-specific manner. Here we report the generation and the functional characterization of a novel mouse model for conditional expression of Cripto, i.e., the Tg:DsRed(loxP/loxP)Cripto-eGFP mice. Moreover, by using a satellite cell specific Cre-driver line we investigated the biological effect of Cripto overexpression in vivo, and provided evidence that overexpression of Cripto in the adult satellite cell compartment promotes myogenic commitment and differentiation, and enhances early regeneration in a mouse model of acute injury. Frontiers Media S.A. 2015-05-21 /pmc/articles/PMC4439575/ /pubmed/26052513 http://dx.doi.org/10.3389/fcell.2015.00031 Text en Copyright © 2015 Prezioso, Iaconis, Andolfi, Zentilin, Iavarone, Guardiola and Minchiotti. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Prezioso, Carolina
Iaconis, Salvatore
Andolfi, Gennaro
Zentilin, Lorena
Iavarone, Francescopaolo
Guardiola, Ombretta
Minchiotti, Gabriella
Conditional Cripto overexpression in satellite cells promotes myogenic commitment and enhances early regeneration
title Conditional Cripto overexpression in satellite cells promotes myogenic commitment and enhances early regeneration
title_full Conditional Cripto overexpression in satellite cells promotes myogenic commitment and enhances early regeneration
title_fullStr Conditional Cripto overexpression in satellite cells promotes myogenic commitment and enhances early regeneration
title_full_unstemmed Conditional Cripto overexpression in satellite cells promotes myogenic commitment and enhances early regeneration
title_short Conditional Cripto overexpression in satellite cells promotes myogenic commitment and enhances early regeneration
title_sort conditional cripto overexpression in satellite cells promotes myogenic commitment and enhances early regeneration
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439575/
https://www.ncbi.nlm.nih.gov/pubmed/26052513
http://dx.doi.org/10.3389/fcell.2015.00031
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