Ng K W, Partridge N C, Niall M, Martin T J
Calcif Tissue Int. 1983 Jul;35(4-5):624-8. doi: 10.1007/BF02405105.
Normal and malignant osteoblast-like cells in culture have been shown to possess specific, high affinity receptors for epidermal growth factor (EGF). In this study, the mitogenic response to EGF was examined in a clonal line of a rat osteogenic sarcoma (UMR 106) and in osteoblast-rich newborn rat calvarial cells. Twenty-four hour treatment of UMR 106 cells with EGF in doses ranging from 10(-12) M to 2 X 10(-8) M stimulated the incorporation of [3H]thymidine and DNA synthesis in a dose-dependent manner. This short-term stimulatory effect was sustained in long-term culture with a dose-dependent increase in cell proliferation by calvarial cells. A lag period of 8 h occurred before significant stimulation of [3H]thymidine incorporation was observed. Commitment to increased incorporation of [3H]thymidine required a minimum of 6 h continuous incubation with EGF. These results establish the osteoblast as a target cell for EGF action on bone.
培养中的正常和成骨样恶性细胞已被证明对表皮生长因子(EGF)具有特异性、高亲和力受体。在本研究中,检测了大鼠骨肉瘤克隆系(UMR 106)和成骨细胞丰富的新生大鼠颅骨细胞对EGF的促有丝分裂反应。用浓度范围为10^(-12) M至2×10^(-8) M的EGF处理UMR 106细胞24小时,以剂量依赖方式刺激了[3H]胸腺嘧啶核苷的掺入和DNA合成。这种短期刺激作用在长期培养中得以维持,颅骨细胞的细胞增殖呈剂量依赖性增加。在观察到[3H]胸腺嘧啶核苷掺入受到显著刺激之前有8小时的延迟期。要使[3H]胸腺嘧啶核苷掺入增加,至少需要与EGF连续孵育6小时。这些结果确定成骨细胞是EGF作用于骨骼的靶细胞。