Nicholson G C, Horton M A, Sexton P M, D'Santos C S, Moseley J M, Kemp B E, Pringle J A, Martin T J
University of Melbourne, Department of Medicine, Repatriation General Hospital, Heidelberg, Victoria, Australia.
Horm Metab Res. 1987 Nov;19(11):585-9. doi: 10.1055/s-2007-1011887.
Osteoclast-rich cultures were prepared by disaggregation of osteoclastomas (giant cell tumour of bone) and settlement onto glass or plastic surfaces. Autoradiography using [125I]-salmon calcitonin ([125I]-sCT) revealed specific binding only to multinucleate giant cells (osteoclasts) and a minor population of mononuclear cells. [125I]-sCT competitive binding studies indicated a Kd of 5 x 10(-10) M and receptor number of approximately 1 million sites/osteoclast. sCT treatment resulted in a dose-dependent rise in cAMP (EC50 10(-10) M). Homogenates of an osteoclastoma also demonstrated specific binding of [125I]-sCT. Chemical cross-linking of a labelled synthetic sCT derivative. [125I]-[Arg11,18,Lys14]-sCT, using disuccinimidyl suberate, resulted in labelling of a receptor component of approximate Mr 85-90,000. The multinucleate giant cells (osteoclasts) of human osteoclastomas possess large number of CT receptors which exhibit the same binding kinetics and apparent Mr as those of other CT target cells.
通过将骨巨细胞瘤(骨巨细胞肿瘤)解离并接种到玻璃或塑料表面制备富含破骨细胞的培养物。使用[125I] - 鲑鱼降钙素([125I] - sCT)的放射自显影显示仅与多核巨细胞(破骨细胞)和少量单核细胞有特异性结合。[125I] - sCT竞争结合研究表明解离常数为5×10(-10)M,受体数量约为100万个位点/破骨细胞。sCT处理导致cAMP呈剂量依赖性升高(半数有效浓度10(-10)M)。骨巨细胞瘤的匀浆也显示出[125I] - sCT的特异性结合。使用辛二酸二琥珀酰亚胺酯对标记的合成sCT衍生物[125I] - [精氨酸11,18,赖氨酸14] - sCT进行化学交联,导致标记出一个分子量约为85 - 90,000的受体成分。人骨巨细胞瘤的多核巨细胞(破骨细胞)拥有大量的降钙素受体,这些受体表现出与其他降钙素靶细胞相同的结合动力学和表观分子量。