Fig. 1From: Advancing osteochondral tissue engineering: bone morphogenetic protein, transforming growth factor, and fibroblast growth factor signaling drive ordered differentiation of periosteal cells resulting in stable cartilage and bone formation in vivoCharacterization of TIs at the gene expression and histological levels. a mRNA quantification by qPCR of chondrogenic genes in tissue intermediates (TIs), control aggregates (CTRL, no GFs) and human articular chondrocytes (hACs). b Longitudinal histological sections (5 μm) of TIs stained for glycosaminoglycans (alcian blue), type-II collagen, type-I collagen, and Indian Hedgehog (IHH) at 14 and 28 days after in vitro culture. Top and bottom layers of TIs are identified by * and **, respectively. Dashed lines represent a critical depth at which cells no longer express type-II collagen or IHH, from top to bottom. Results are representative of two independent experiments. Each experiment was performed using 2–3 technical replicates. In a, error bars are max/min; *P < 0.05, **P < 0.01, ***P < 0.001Back to article page