Hwang Nathaniel S, Varghese Shyni, Puleo Christopher, Zhang Zijun, Elisseeff Jennifer
Department of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland, USA.
J Cell Physiol. 2007 Aug;212(2):281-4. doi: 10.1002/jcp.21052.
Mesenchymal stem cells (MSCs) are potentially useful cells for musculoskeletal tissue engineering. However, controlling MSC differentiation and tissue formation in vivo remains a challenge. There is a significant need for well-defined and efficient protocols for directing MSC behaviors in vivo. We hypothesize that morphogenetic signals from chondrocytes may regulate MSC differentiation. In micromass culture of MSCs, incubation with chondrocyte-conditioned medium (CCM) significantly enhanced the production of cartilage specific matrix including type II collagen. In addition, incubation of MSCs with conditioned medium supplemented with osteogenic factors induced more osteogenesis and accumulation of calcium and increased ALP activity. These findings reveal that chondrocyte-secreted factors promote chondrogenesis as well as osteogenesis of MSCs during in vitro micromass culture. Moreover, when MSCs expanded with chondrocyte-conditioned medium were encapsulated in hydrogels and subsequently implanted into athymic mice, basophilic extracellular matrix deposition characteristic of neocartilage was evident. These results indicate that articular chondrocytes produce suitable morphogenetic factors that induce the differentiation program of MSCs in vitro and in vivo.
间充质干细胞(MSCs)是用于肌肉骨骼组织工程的潜在有用细胞。然而,在体内控制MSC分化和组织形成仍然是一项挑战。迫切需要明确且有效的方案来指导体内MSC的行为。我们假设来自软骨细胞的形态发生信号可能调节MSC分化。在MSCs的微团培养中,用软骨细胞条件培养基(CCM)孵育可显著增强包括II型胶原蛋白在内的软骨特异性基质的产生。此外,用补充有成骨因子的条件培养基孵育MSCs可诱导更多的成骨作用以及钙的积累,并增加碱性磷酸酶(ALP)活性。这些发现表明,在体外微团培养期间,软骨细胞分泌的因子可促进MSCs的软骨生成以及成骨作用。此外,当用软骨细胞条件培养基扩增的MSCs被包裹在水凝胶中并随后植入无胸腺小鼠体内时,新软骨特有的嗜碱性细胞外基质沉积很明显。这些结果表明,关节软骨细胞产生合适的形态发生因子,可在体外和体内诱导MSCs的分化程序。