A team at the Mechanobiology Institute, National University of Singapore, engineers hybrid polyacrylamide–ECM scaffolds that decellularize heart tissue in situ and tune stiffness independently to probe age-related biochemical and mechanical effects on cardiac fibroblasts.
Key points
- DECIPHER embeds thin murine heart slices in acrylamide pretreated with formaldehyde to form stable polyacrylamide–ECM hybrids while preserving native ligand distribution.
- Hydrogel formulations are tuned to Young’s moduli of ~10 kPa or ~40 kPa, replicating young and aged cardiac tissue stiffness independently of ECM composition.
- Young ECM ligand presentation overrides profibrotic stiffness in maintaining cardiac fibroblast quiescence; aged ECM drives activation and senescence through specific receptor and mechanotransduction pathways.
Why it matters: This platform decouples biochemical ligands and mechanics in aged cardiac ECM, offering precise targets for anti-fibrotic and rejuvenation therapies.
Q&A
- What is a hybrid hydrogel–ECM scaffold?
- How does DECIPHER preserve native ECM properties?
- Why study mechanical stiffness and ligand cues separately?
- What role do cardiac fibroblasts play in heart aging?