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Dynamics of Cellular States of Fibro-adipogenic Progenitors During Myogenesis and Muscular Dystrophy

Overview
Journal Nat Commun
Specialty Biology
Date 2018 Sep 12
PMID 30202063
Citations 109
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Abstract

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 or Tie2 and Tie2/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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References
1.
Dulauroy S, Di Carlo S, Langa F, Eberl G, Peduto L . Lineage tracing and genetic ablation of ADAM12(+) perivascular cells identify a major source of profibrotic cells during acute tissue injury. Nat Med. 2012; 18(8):1262-70. DOI: 10.1038/nm.2848. View

2.
Fiore D, Judson R, Low M, Lee S, Zhang E, Hopkins C . Pharmacological blockage of fibro/adipogenic progenitor expansion and suppression of regenerative fibrogenesis is associated with impaired skeletal muscle regeneration. Stem Cell Res. 2016; 17(1):161-9. DOI: 10.1016/j.scr.2016.06.007. View

3.
Dumont N, Wang Y, von Maltzahn J, Pasut A, Bentzinger C, Brun C . Dystrophin expression in muscle stem cells regulates their polarity and asymmetric division. Nat Med. 2015; 21(12):1455-63. PMC: 4839960. DOI: 10.1038/nm.3990. View

4.
Kharraz Y, Guerra J, Mann C, Serrano A, Munoz-Canoves P . Macrophage plasticity and the role of inflammation in skeletal muscle repair. Mediators Inflamm. 2013; 2013:491497. PMC: 3572642. DOI: 10.1155/2013/491497. View

5.
Darby I, Zakuan N, Billet F, Desmouliere A . The myofibroblast, a key cell in normal and pathological tissue repair. Cell Mol Life Sci. 2015; 73(6):1145-57. PMC: 11108523. DOI: 10.1007/s00018-015-2110-0. View