Jiao Y, Wang D, Tian W
College of Stomatology, West China University of Medical Sciences, Chengdu, Sichuan, China.
Hua Xi Kou Qiang Yi Xue Za Zhi. 1997 Aug;15(3):187-9.
To investigate the behavoir of TMJ condylar cartilage cells in vitro, the mandibular condylar cartilage cells were harvested from a 5-month-old human fetus by dissection and sequential digestion with 0.25% trypsin and 0.2% collagenase (type II). The isolated cells were cultured in DMEM medium and identified by histochemical and immunohistochemical methods. Cell proliferation, morphology and ultrastructure were observed by phase-contrast microscope, cytologic staining and electronic microscope. In primarily cultured cells, polygonal chondroblast-like cells dominated and they were confirmed by the positive result of immunohistochemical examination for type II collagen and Toludin blue staining. In conclusion, the TMJ cells in this culture system kept their phenotype in vivo.
为研究颞下颌关节髁突软骨细胞的体外行为,通过解剖并先后用0.25%胰蛋白酶和0.2%Ⅱ型胶原酶消化,从一名5个月大的人类胎儿获取下颌髁突软骨细胞。将分离出的细胞培养于DMEM培养基中,并通过组织化学和免疫组织化学方法进行鉴定。通过相差显微镜、细胞染色和电子显微镜观察细胞增殖、形态和超微结构。在原代培养细胞中,多边形成软骨细胞样细胞占主导,Ⅱ型胶原免疫组织化学检查阳性结果及甲苯胺蓝染色证实了这一点。总之,该培养系统中的颞下颌关节细胞在体内保持了其表型。