| Literature DB >> 27063490 |
Nathalie Luciani1, Vicard Du2, Florence Gazeau2, Alain Richert2, Didier Letourneur3, Catherine Le Visage4, Claire Wilhelm2.
Abstract
UNLABELLED: Tissue engineering strategies, such as cellularized scaffolds approaches, have been explored for cartilage replacement. The challenge, however, remains to produce a cartilaginous tissue incorporating functional chondrocytes and being large and thick enough to be compatible with the replacement of articular defects. Here, we achieved unprecedented cartilage tissue production into a porous polysaccharide scaffold by combining of efficient magnetic condensation of mesenchymal stem cells, and dynamic maturation in a bioreactor. In optimal conditions, all the hallmarks of chondrogenesis were enhanced with a 50-fold increase in collagen II expression compared to negative control, an overexpression of aggrecan and collagen XI, and a very low expression of collagen I and RUNX2. Histological staining showed a large number of cellular aggregates, as well as an increased proteoglycan synthesis by chondrocytes. Interestingly, electron microscopy showed larger chondrocytes and a more abundant extracellular matrix. In addition, the periodicity of the neosynthesized collagen fibers matched that of collagen II. These results represent a major step forward in replacement tissue for cartilage defects. STATEMENT OF SIGNIFICANCE: A combination of several innovative technologies (magnetic cell seeding, polysaccharide porous scaffolds, and dynamic maturation in bioreactor) enabled unprecedented successful chondrogenesis within scaffolds.Entities:
Keywords: Bioreactor; Cartilage defect; Chondrogenesis; Magnetic mesenchymal stem cells; Tissue engineering
Mesh:
Year: 2016 PMID: 27063490 DOI: 10.1016/j.actbio.2016.04.009
Source DB: PubMed Journal: Acta Biomater ISSN: 1742-7061 Impact factor: 8.947