Fibroblast-specific TGF-β–Smad2/3 signaling underlies cardiac fibrosis
Cincinnati Children's Hospital Medical Center · University of Cincinnati · +4 more institutions
Abstract
The master cytokine TGF-β mediates tissue fibrosis associated with inflammation and tissue injury. TGF-β induces fibroblast activation and differentiation into myofibroblasts that secrete extracellular matrix proteins. Canonical TGF-β signaling mobilizes Smad2 and Smad3 transcription factors that control fibrosis by promoting gene expression. However, the importance of TGF-β-Smad2/3 signaling in fibroblast-mediated cardiac fibrosis has not been directly evaluated in vivo. Here, we examined pressure overload-induced cardiac fibrosis in fibroblast- and myofibroblast-specific inducible Cre-expressing mouse lines with selective deletion of the TGF-β receptors Tgfbr1/2, Smad2, or Smad3. Fibroblast-specific deletion…
Citation impact
- FWCI
- 37.56
- Percentile
- 100%
- References
- 66
Authors
12- HKHadi Khalil
Cincinnati Children's Hospital Medical Center, University of Cincinnati
- OKOnur Kanisicak
Cincinnati Children's Hospital Medical Center, University of Cincinnati
- VPVikram Prasad
Cincinnati Children's Hospital Medical Center, University of Cincinnati
- RNRobert N. Correll
Cincinnati Children's Hospital Medical Center, University of Cincinnati
- XFXing Fu
Cincinnati Children's Hospital Medical Center, University of Cincinnati
Topics & keywords
- Fibrosis
- Cardiac fibrosis
- Fibroblast
- Myofibroblast
- Extracellular matrix
- Biology
- Cell biology
- Pressure overload
- Good health and well-being