Dynamics of cellular states of fibro-adipogenic progenitors during myogenesis and muscular dystrophy.
Barbora MalecovaSole GattoUsue EtxanizMagda PassafaroAmy CortezChiara NicolettiLorenzo GiordaniAlessio TorcinaroMarco De BardiSilvio BicciatoFrancesca De SantaLuca MadaroPier Lorenzo PuriPublished in: Nature communications (2018)
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 Tie2high or Tie2low and Tie2low/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.
Keyphrases
- duchenne muscular dystrophy
- single cell
- muscular dystrophy
- rna seq
- cell adhesion
- inflammatory response
- liver failure
- oxidative stress
- respiratory failure
- transcription factor
- high throughput
- induced apoptosis
- cell therapy
- poor prognosis
- drug induced
- aortic dissection
- systemic sclerosis
- gene expression
- adipose tissue
- genome wide identification
- genome wide
- idiopathic pulmonary fibrosis
- stem cells
- intensive care unit
- lipopolysaccharide induced
- immune response
- toll like receptor
- cell death
- lps induced
- hepatitis b virus
- long non coding rna
- acute respiratory distress syndrome
- heat shock protein