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Calcitonin receptors of human osteoclastoma
Authors:G C Nicholson  M A Horton  P M Sexton  C S D'Santos  J M Moseley  B E Kemp  J A Pringle  T J Martin
Institution:University of Melbourne, Department of Medicine, Repatriation General Hospital, Heidelberg, Victoria, Australia.
Abstract: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.
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