Conover C A, Misra P, Hintz R L, Rosenfeld R G
Biochem Biophys Res Commun. 1986 Sep 14;139(2):501-8. doi: 10.1016/s0006-291x(86)80019-5.
To investigate the role of insulin-like growth factor II in the control of DNA synthesis in human fibroblasts, dose-response curves for insulin-like growth factor I and II stimulation of [3H]thymidine incorporation were compared in the absence and presence of alpha IR-3, a highly specific monoclonal antibody directed against the type I insulin-like growth factor receptor. Specific binding of [125I]insulin-like growth factor I to human fibroblast monolayer cultures was inhibited 60-70% in the presence of alpha IR-3. alpha IR-3 had no effect on [125I]insulin-like growth factor II binding to human fibroblasts. However, alpha IR-3 inhibited both insulin-like growth factor I and II stimulated [3H]thymidine incorporation. These data indicate that the type II insulin-like growth factor receptor does not function as a transducer of insulin-like growth factor II's mitogenic effect in human fibroblasts.
为研究胰岛素样生长因子II在调控人成纤维细胞DNA合成中的作用,在不存在和存在αIR-3(一种针对I型胰岛素样生长因子受体的高度特异性单克隆抗体)的情况下,比较了胰岛素样生长因子I和II刺激[3H]胸腺嘧啶核苷掺入的剂量反应曲线。在αIR-3存在的情况下,[125I]胰岛素样生长因子I与人成纤维细胞单层培养物的特异性结合被抑制了60 - 70%。αIR-3对[125I]胰岛素样生长因子II与人成纤维细胞的结合没有影响。然而,αIR-3抑制了胰岛素样生长因子I和II刺激的[3H]胸腺嘧啶核苷掺入。这些数据表明,II型胰岛素样生长因子受体在人成纤维细胞中并非作为胰岛素样生长因子II促有丝分裂作用的转导器发挥功能。