Porous decellularized tissue engineered hypertrophic cartilage as a scaffold for large bone defect healing. (1st September 2015)

• Record Type: Journal Article
• Authors: Cunniffe, Gráinne M.; Vinardell, Tatiana; Murphy, J. Mary; Thompson, Emmet M.; Matsiko, Amos; O'Brien, Fergal J.; Kelly, Daniel J.
• Is Part Of: Acta biomaterialia. Volume 23(2015)
• Page Start: 82
• Page End: 90
• Publication Date: 2015-09-01
• Subjects: Hypertrophic cartilage -- Decellularized scaffold -- Extracellular matrix -- Endochondral ossification -- Large bone defect; Biomedical materials -- Periodicals; 610.28
• DOI: 10.1016/j.actbio.2015.05.031
• Languages: English
• ISSNs: 1742-7061

Abstract

Graphical abstract: Abstract: Clinical translation of tissue engineered therapeutics is hampered by the significant logistical and regulatory challenges associated with such products, prompting increased interest in the use of decellularized extracellular matrix (ECM) to enhance endogenous regeneration. Most bones develop and heal by endochondral ossification, the replacement of a hypertrophic cartilaginous intermediary with bone. The hypothesis of this study is that a porous scaffold derived from decellularized tissue engineered hypertrophic cartilage will retain the necessary signals to instruct host cells to accelerate endogenous bone regeneration. Cartilage tissue (CT) and hypertrophic cartilage tissue (HT) were engineered using human bone marrow derived mesenchymal stem cells, decellularized and the remaining ECM was freeze-dried to generate porous scaffolds. When implanted subcutaneously in nude mice, only the decellularized HT-derived scaffolds were found to induce vascularization and de novo mineral accumulation. Furthermore, when implanted into critically-sized femoral defects, full bridging was observed in half of the defects treated with HT scaffolds, while no evidence of such bridging was found in empty controls. Host cells which had migrated throughout the scaffold were capable of producing new bone tissue, in contrast to fibrous tissue formation within empty controls. These results demonstrate the capacity of decellularized engineered tissues as 'off-the-shelf' implants to promote tissue regeneration.