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Dynamics of cellular states of fibro-adipogenic progenitors during myogenesis and muscular dystrophy

Fibro-adipogenic progenitors (FAPs) are currently defined by their anatomical position, expression of non-specific membrane-associated proteins, and ability to adopt multiple lineages in vitro. Gene expression analysis at single-cell level reveals that FAPs undergo dynamic transitions through a spec...

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Autores principales: Malecova, Barbora, Gatto, Sole, Etxaniz, Usue, Passafaro, Magda, Cortez, Amy, Nicoletti, Chiara, Giordani, Lorenzo, Torcinaro, Alessio, De Bardi, Marco, Bicciato, Silvio, De Santa, Francesca, Madaro, Luca, Puri, Pier Lorenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131350/
https://www.ncbi.nlm.nih.gov/pubmed/30202063
http://dx.doi.org/10.1038/s41467-018-06068-6
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author Malecova, Barbora
Gatto, Sole
Etxaniz, Usue
Passafaro, Magda
Cortez, Amy
Nicoletti, Chiara
Giordani, Lorenzo
Torcinaro, Alessio
De Bardi, Marco
Bicciato, Silvio
De Santa, Francesca
Madaro, Luca
Puri, Pier Lorenzo
author_facet Malecova, Barbora
Gatto, Sole
Etxaniz, Usue
Passafaro, Magda
Cortez, Amy
Nicoletti, Chiara
Giordani, Lorenzo
Torcinaro, Alessio
De Bardi, Marco
Bicciato, Silvio
De Santa, Francesca
Madaro, Luca
Puri, Pier Lorenzo
author_sort Malecova, Barbora
collection PubMed
description Fibro-adipogenic progenitors (FAPs) are currently defined by their anatomical position, expression of non-specific membrane-associated proteins, and ability to adopt multiple lineages in vitro. Gene expression analysis at single-cell level reveals that FAPs undergo dynamic transitions through a spectrum of cell states that can be identified by differential expression levels of Tie2 and Vcam1. Different patterns of Vcam1-negative Tie2(high) or Tie2(low) and Tie2(low)/Vcam1-expressing FAPs are detected during neonatal myogenesis, response to acute injury and Duchenne Muscular Dystrophy (DMD). RNA sequencing analysis identified cell state-specific transcriptional profiles that predict functional interactions with satellite and inflammatory cells. In particular, Vcam1-expressing FAPs, which exhibit a pro-fibrotic expression profile, are transiently activated by acute injury in concomitance with the inflammatory response. Aberrant persistence of Vcam1-expressing FAPs is detected in DMD muscles or upon macrophage depletion, and is associated with muscle fibrosis, thereby revealing how disruption of inflammation-regulated FAPs dynamics leads to a pathogenic outcome.
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spelling pubmed-61313502018-09-12 Dynamics of cellular states of fibro-adipogenic progenitors during myogenesis and muscular dystrophy Malecova, Barbora Gatto, Sole Etxaniz, Usue Passafaro, Magda Cortez, Amy Nicoletti, Chiara Giordani, Lorenzo Torcinaro, Alessio De Bardi, Marco Bicciato, Silvio De Santa, Francesca Madaro, Luca Puri, Pier Lorenzo Nat Commun Article Fibro-adipogenic progenitors (FAPs) are currently defined by their anatomical position, expression of non-specific membrane-associated proteins, and ability to adopt multiple lineages in vitro. Gene expression analysis at single-cell level reveals that FAPs undergo dynamic transitions through a spectrum of cell states that can be identified by differential expression levels of Tie2 and Vcam1. Different patterns of Vcam1-negative Tie2(high) or Tie2(low) and Tie2(low)/Vcam1-expressing FAPs are detected during neonatal myogenesis, response to acute injury and Duchenne Muscular Dystrophy (DMD). RNA sequencing analysis identified cell state-specific transcriptional profiles that predict functional interactions with satellite and inflammatory cells. In particular, Vcam1-expressing FAPs, which exhibit a pro-fibrotic expression profile, are transiently activated by acute injury in concomitance with the inflammatory response. Aberrant persistence of Vcam1-expressing FAPs is detected in DMD muscles or upon macrophage depletion, and is associated with muscle fibrosis, thereby revealing how disruption of inflammation-regulated FAPs dynamics leads to a pathogenic outcome. Nature Publishing Group UK 2018-09-10 /pmc/articles/PMC6131350/ /pubmed/30202063 http://dx.doi.org/10.1038/s41467-018-06068-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Malecova, Barbora
Gatto, Sole
Etxaniz, Usue
Passafaro, Magda
Cortez, Amy
Nicoletti, Chiara
Giordani, Lorenzo
Torcinaro, Alessio
De Bardi, Marco
Bicciato, Silvio
De Santa, Francesca
Madaro, Luca
Puri, Pier Lorenzo
Dynamics of cellular states of fibro-adipogenic progenitors during myogenesis and muscular dystrophy
title Dynamics of cellular states of fibro-adipogenic progenitors during myogenesis and muscular dystrophy
title_full Dynamics of cellular states of fibro-adipogenic progenitors during myogenesis and muscular dystrophy
title_fullStr Dynamics of cellular states of fibro-adipogenic progenitors during myogenesis and muscular dystrophy
title_full_unstemmed Dynamics of cellular states of fibro-adipogenic progenitors during myogenesis and muscular dystrophy
title_short Dynamics of cellular states of fibro-adipogenic progenitors during myogenesis and muscular dystrophy
title_sort dynamics of cellular states of fibro-adipogenic progenitors during myogenesis and muscular dystrophy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131350/
https://www.ncbi.nlm.nih.gov/pubmed/30202063
http://dx.doi.org/10.1038/s41467-018-06068-6
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