Cargando…
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...
Autores principales: | , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1783354086287998976 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6131350 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT malecovabarbora dynamicsofcellularstatesoffibroadipogenicprogenitorsduringmyogenesisandmusculardystrophy AT gattosole dynamicsofcellularstatesoffibroadipogenicprogenitorsduringmyogenesisandmusculardystrophy AT etxanizusue dynamicsofcellularstatesoffibroadipogenicprogenitorsduringmyogenesisandmusculardystrophy AT passafaromagda dynamicsofcellularstatesoffibroadipogenicprogenitorsduringmyogenesisandmusculardystrophy AT cortezamy dynamicsofcellularstatesoffibroadipogenicprogenitorsduringmyogenesisandmusculardystrophy AT nicolettichiara dynamicsofcellularstatesoffibroadipogenicprogenitorsduringmyogenesisandmusculardystrophy AT giordanilorenzo dynamicsofcellularstatesoffibroadipogenicprogenitorsduringmyogenesisandmusculardystrophy AT torcinaroalessio dynamicsofcellularstatesoffibroadipogenicprogenitorsduringmyogenesisandmusculardystrophy AT debardimarco dynamicsofcellularstatesoffibroadipogenicprogenitorsduringmyogenesisandmusculardystrophy AT bicciatosilvio dynamicsofcellularstatesoffibroadipogenicprogenitorsduringmyogenesisandmusculardystrophy AT desantafrancesca dynamicsofcellularstatesoffibroadipogenicprogenitorsduringmyogenesisandmusculardystrophy AT madaroluca dynamicsofcellularstatesoffibroadipogenicprogenitorsduringmyogenesisandmusculardystrophy AT puripierlorenzo dynamicsofcellularstatesoffibroadipogenicprogenitorsduringmyogenesisandmusculardystrophy |