Takano-Yamamoto T, Nakagawa K, Shimada T, Sakuda M
Department of Orthodontics, Osaka University Faculty of Dentistry, Japan.
J Osaka Univ Dent Sch. 1993 Dec;33:1-8.
Previously, we reported methods for isolating chondrocytes from the craniofacial cartilage and culturing them in vitro. The cells actively synthesize glycosaminoglycan (GAG), a marker of the differentiated phenotype of chondrocytes and respond well to PTH and glucocorticoids. It has been suggested that chondrocytes produce somatomedin-like growth factors which support their own growth and GAG synthesis. In the present study, we reported studies on the effect of conditioned medium obtained from cultures of rabbit craniofacial chondrocytes on GAG and DNA syntheses in the same chondrocyte cultures. Serum-free medium, conditioned by exposure to rabbit chondrocytes from mandibular condyle, nasal septum and sphenooccipital synchondrosis in monolayer culture stimulated not only the synthesis of GAG by the same cells but also their own DNA synthesis. The stimulation of the syntheses of GAG and DNA by the conditioned-medium factor were concentration-dependent. In addition, these three kinds of conditioned media stimulated GAG and DNA syntheses of other types of chondrocytes. These findings suggest that rabbit chondrocytes from the craniofacial complex release factors into the culture medium that enhance their own growth and expression of the differentiated phenotype of chondrocytes as well as that of costal chondrocytes.
此前,我们报道了从颅面软骨中分离软骨细胞并在体外培养的方法。这些细胞能积极合成糖胺聚糖(GAG),这是软骨细胞分化表型的一个标志物,并且对甲状旁腺激素(PTH)和糖皮质激素反应良好。有人提出软骨细胞会产生类生长激素介质样生长因子,以支持其自身生长和GAG合成。在本研究中,我们报告了关于从兔颅面软骨细胞培养物中获得的条件培养基对相同软骨细胞培养物中GAG和DNA合成影响的研究。通过单层培养中暴露于来自下颌髁、鼻中隔和蝶枕软骨结合处的兔软骨细胞而条件化的无血清培养基,不仅刺激了相同细胞的GAG合成,还刺激了它们自身的DNA合成。条件培养基因子对GAG和DNA合成的刺激是浓度依赖性的。此外,这三种条件培养基刺激了其他类型软骨细胞的GAG和DNA合成。这些发现表明,来自颅面复合体的兔软骨细胞向培养基中释放因子,这些因子可增强其自身生长以及软骨细胞和肋软骨细胞分化表型的表达。