Bulk RNA-seq of CD248+/- PDGFR-α+ cardiac fibroblasts
Ontology highlight
ABSTRACT:
PROVIDER: PRJNA1212032 | ENA |
REPOSITORIES: ENA
Dataset's files
| Action | DRS | |||
|---|---|---|---|---|
| SRR32033500_1.fastq.gz | Fastqsanger.gz | |||
| SRR32033500_2.fastq.gz | Fastqsanger.gz | |||
| SRR32033493_1.fastq.gz | Fastqsanger.gz | |||
| SRR32033493_2.fastq.gz | Fastqsanger.gz | |||
| SRR32033494_1.fastq.gz | Fastqsanger.gz |
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Project description:The interstitial and perivascular spaces of the heart contain stem-like cells including cardiac colony forming units - fibroblast (cCFU-F), a sub-fraction of SCA1+PDGFR-alpha +CD31- (S+P+) immature stromal cells with the qualities of mesenchymal stem cells, that we have characterized previously. Here we explore the role of platelet-derived growth factor receptor (PDGFR-alpha in cCFU-F and S+P+ cell niche regulation in homeostasis and repair. PDGFR-alpha signaling modulated quiescence, metabolic state, mitogenic propensity and colony formation, as well as the rate and stability of self-renewal. Exogenously administered PDGF-AB ligand had anti-aging effects on cCFU-F, akin to those seen in heterochronic parabiotic mice. Post-myocardial infarction (MI), PDGF-AB stimulated S+P+ cell proliferation and conversion to myofibroblasts through a metabolic priming effect, yet significantly enhanced anatomical and functional repair via multiple cellular processes. Our study provides a rationale for a novel therapeutic approach to cardiac injury involving stimulating endogenous repair mechanisms via activation of cardiac stem and stromal cells.
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