Endothelial cell signature in muscle stem cells validated by VEGFA-FLT1-AKT1 axis promoting survival of muscle stem cell.
Mayank VermaYoko AsakuraXuerui WangKasey ZhouMahmut ÜnverdiAllison P KannRobert S KraussAtsushi AsakuraPublished in: eLife (2024)
Endothelial and skeletal muscle lineages arise from common embryonic progenitors. Despite their shared developmental origin, adult endothelial cells (ECs) and muscle stem cells (MuSCs) (satellite cells) have been thought to possess distinct gene signatures and signaling pathways. Here we shift this paradigm by uncovering how adult MuSC behavior is affected by the expression of a subset of EC transcripts. We used several computational analyses including single-cell RNAseq to show that MuSCs express low levels of canonical EC markers in mice. We demonstrate that MuSC survival is regulated by one such prototypic endothelial signaling pathway (VEGFA-FLT1). Using pharmacological and genetic gain- and loss-of-function studies, we identify the FLT1-AKT1 axis as the key effector underlying VEGFA-mediated regulation of MuSC survival. All together, our data support that the VEGFA-FLT1-AKT1 pathway promotes MuSC survival during muscle regeneration, and highlights how the minor expression of select transcripts is sufficient for affecting cell behavior.
Keyphrases
- stem cells
- signaling pathway
- skeletal muscle
- endothelial cells
- acute myeloid leukemia
- induced apoptosis
- single cell
- tyrosine kinase
- cell therapy
- pi k akt
- cell proliferation
- free survival
- poor prognosis
- genome wide
- insulin resistance
- epithelial mesenchymal transition
- high glucose
- cell cycle arrest
- rna seq
- binding protein
- type diabetes
- copy number
- endoplasmic reticulum stress
- electronic health record
- cell death
- immune response
- deep learning
- vascular endothelial growth factor
- machine learning
- mesenchymal stem cells
- adipose tissue
- artificial intelligence