Hypoxic culture of bone marrow-derived mesenchymal stromal stem cells differentially enhances in vitro chondrogenesis within cell-seeded collagen and hyaluronic acid porous scaffolds

Troy D Bornes, Nadr M Jomha, Aillette Mulet-Sierra, Adetola B Adesida

Quality of cartilaginous tissue derived from bone marrow mesenchymal stromal stem cell (BMSC) transplantation has been correlated with clinical outcome. Therefore, culture conditions capable of modulating tissue phenotype, such as oxygen tension and scaffold composition, are under investigation. The objective of this study was to assess the effect of hypoxia on in vitro BMSC chondrogenesis within clinically approved porous scaffolds composed of collagen and hyaluronic acid (HA). It was hypothesized that hypoxic isolation/expansion and differentiation would improve BMSC chondrogenesis in each construct. Ovine BMSCs were isolated and expanded to passage two under hypoxia (3% oxygen) or normoxia (21% oxygen). Cell proliferation and colony forming characteristics were assessed. BMSCs were seeded at 10 million cells/cm(3) on cylindrical scaffolds composed of either collagen I sponge or esterified hyaluronic acid (HA) non-woven mesh. Chondrogenic differentiation was performed in a defined medium under hypoxia or normoxia for 14 days. Cultured constructs were assessed for gene expression, proteoglycan staining, glycosaminoglycan (GAG) quantity, and diameter change. Isolation/expansion under hypoxia resulted in faster BMSC population doublings per day (p < 0.05), while cell and colony counts were not significantly different (p = 0.60 and 0.30, respectively). Collagen and HA scaffolds seeded with BMSCs that were isolated, expanded and differentiated under hypoxia exhibited superior aggrecan and collagen II mRNA expressions (p < 0.05), GAG quantity (p < 0.05) and proteoglycan staining in comparison to normoxia. GAG/DNA was augmented with hypoxic isolation/expansion in all constructs (p < 0.01). Comparison by scaffold composition indicated increased mRNA expressions of hyaline cartilage-associated collagen II, aggrecan and SOX9 in collagen scaffolds, although expression of collagen X, which is related to hypertrophic cartilage, was also elevated (p < 0.05). Proteoglycan deposition was not significantly improved in collagen scaffolds unless culture involved normoxic isolation/expansion followed by hypoxic differentiation. During chondrogenesis, collagen-based constructs progressively contracted to 60.1 ± 8.9% of the initial diameter after 14 days, while HA-based construct size was maintained (109.7 ± 4.2%). Hypoxic isolation/expansion and differentiation enhance in vitro BMSC chondrogenesis within porous scaffolds. Although both collagen I and HA scaffolds support the creation of hyaline-like cartilaginous tissue, variations in gene expression, extracellular matrix formation and construct size occur during chondrogenesis.