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Single-cell transcriptomic analysis of the identity and function of fibro/adipogenic progenitors in healthy and dystrophic muscle.
Uapinyoying, Prech; Hogarth, Marshall; Battacharya, Surajit; Mázala, Davi A G; Panchapakesan, Karuna; Bönnemann, Carsten G; Jaiswal, Jyoti K.
Afiliação
  • Uapinyoying P; Center for Genetic Medicine Research, Children's National Research and Innovation Campus, Children's National Hospital, Washington, DC 20012, USA.
  • Hogarth M; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.
  • Battacharya S; Center for Genetic Medicine Research, Children's National Research and Innovation Campus, Children's National Hospital, Washington, DC 20012, USA.
  • Mázala DAG; Center for Genetic Medicine Research, Children's National Research and Innovation Campus, Children's National Hospital, Washington, DC 20012, USA.
  • Panchapakesan K; Center for Genetic Medicine Research, Children's National Research and Innovation Campus, Children's National Hospital, Washington, DC 20012, USA.
  • Bönnemann CG; Department of Kinesiology, College of Health Professions, Towson University, Towson, MD 21252, USA.
  • Jaiswal JK; Center for Genetic Medicine Research, Children's National Research and Innovation Campus, Children's National Hospital, Washington, DC 20012, USA.
iScience ; 26(8): 107479, 2023 Aug 18.
Article em En | MEDLINE | ID: mdl-37599828
ABSTRACT
Fibro/adipogenic progenitors (FAPs) are skeletal muscle stromal cells that support regeneration of injured myofibers and their maintenance in healthy muscles. FAPs are related to mesenchymal stem cells (MSCs/MeSCs) found in other adult tissues, but there is poor understanding of the extent of similarity between these cells. Using single-cell RNA sequencing (scRNA-seq) datasets from multiple mouse tissues, we have performed comparative transcriptomic analysis. This identified remarkable transcriptional similarity between FAPs and MeSCs, confirmed the suitability of PDGFRα as a reporter for FAPs, and identified extracellular proteolysis as a new FAP function. Using PDGFRα as a cell surface marker, we isolated FAPs from healthy and dysferlinopathic mouse muscles and performed scRNA-seq analysis. This revealed decreased FAP-mediated Wnt signaling as a potential driver of FAP dysfunction in dysferlinopathic muscles. Analysis of FAPs in dysferlin- and dystrophin-deficient muscles identified a relationship between the nature of muscle pathology and alteration in FAP gene expression.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article