Single-cell transcriptomic analysis of the identity and function of fibro/adipogenic progenitors in healthy and dystrophic muscle

被引:4
|
作者
Uapinyoying, Prech [1 ,2 ]
Hogarth, Marshall [1 ]
Battacharya, Surajit [1 ]
Mazala, Davi A. G. [1 ,3 ]
Panchapakesan, Karuna [1 ]
Bonnemann, Carsten G. [2 ]
Jaiswal, Jyoti K. [1 ,4 ]
机构
[1] Childrens Natl Hosp, Ctr Genet Med Res, Childrens Natl Res & Innovat Campus, Washington, DC 20012 USA
[2] NINDS, Neuromuscular & Neurogenet Disorders Childhood Sec, NIH, Bethesda, MD 20892 USA
[3] Towson Univ, Coll Hlth Profess, Dept Kinesiol, Towson, MD 21252 USA
[4] George Washington Univ, Sch Med & Hlth Sci, Dept Genom & Precis Med, Washington, DC 20052 USA
关键词
SKELETAL-MUSCLE; SATELLITE CELLS; EXPRESSION; INHIBITION; RECEPTOR; REPEATS; PROTEIN; PREF-1; WNT;
D O I
10.1016/j.isci.2023.107479
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 PDGFR alpha as a reporter for FAPs, and identified extracellular proteolysis as a new FAP function. Using PDGFR alpha 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.
引用
收藏
页数:21
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