Levy J, Shimshoni Z, Somjen D, Berger E, Fine N, Silbermann M, Binderman I
Department of Orthodontics, Maurice and Gabriela Goldschleger School of Dental Medicine, Tel Aviv University, Israel.
In Vitro Cell Dev Biol. 1988 Jul;24(7):620-4. doi: 10.1007/BF02623598.
Cell cultures derived from young rat epiphyseal cartilage were grown for approximately 2 wk in BGJb medium supplemented with 10% fetal bovine serum to reach confluence. These cells were identified as chondrocytes as checked by morphology, the presence of alkaline phosphatase, and a positive type II collagen antibody reaction. The cells also responded to different hormonal treatment. Parathyroid hormone (PTH) increased cyclic AMP production by 50% within 15 min of treatment, whereas prostaglandin E2 (PGE2) caused an increase of 160%. Calcitonin (CT) did not affect cAMP production in these cells. DNA synthesis 24 h after hormonal treatment was increased by PTH (2.5-fold) and PGE2 (2-fold), but not by CT. Among the vitamin D metabolites, 24,25(OH)2D3 increased significantly the [3H]thymidine incorporation into DNA, whereas 1,25(OH)2D3 effect was minimal. These results provide evidence for the use of these cell cultures as a model for cartilage in vitro when studying biological and hormonal responsiveness.
从幼鼠骺软骨获取的细胞培养物在补充有10%胎牛血清的BGJb培养基中培养约2周以达到汇合。通过形态学、碱性磷酸酶的存在以及II型胶原抗体阳性反应检查,这些细胞被鉴定为软骨细胞。这些细胞也对不同的激素处理有反应。甲状旁腺激素(PTH)在处理后15分钟内使环磷酸腺苷(cAMP)产量增加50%,而前列腺素E2(PGE2)使产量增加160%。降钙素(CT)对这些细胞中的cAMP产量没有影响。激素处理24小时后的DNA合成在PTH(2.5倍)和PGE2(2倍)作用下增加,但CT没有此作用。在维生素D代谢物中,24,25(OH)2D3显著增加了[3H]胸腺嘧啶核苷掺入DNA,而1,25(OH)2D3的作用最小。这些结果为在研究生物学和激素反应性时将这些细胞培养物用作体外软骨模型提供了证据。