Chowdhury M H, Shen V, Dempster D W
Regional Bone Center, Helen Hayes Hospital, New York State Dept. of Health, West Haverstraw 10993.
Calcif Tissue Int. 1991 Oct;49(4):275-9. doi: 10.1007/BF02556217.
We have studied the effects of cyclosporine A (CsA) on basal and bovine parathyroid hormone (1-34) (bPTH)-stimulated bone resorption by osteoclasts in 24-hour cultures of chick long bone cells. At a high concentration (10 micrograms/ml), CsA had a cytotoxic effect on both osteoclasts and mononuclear cells in the culture. At 1 microgram/ml, CsA inhibited basal and bPTH-stimulated bone resorption but was not cytotoxic over 24 hours. We also studied the binding of bPTH to the osteoblastic cell line, Saos-2, and chick long bone cells in suspension culture. CsA inhibited bPTH binding in Saos-2 in a dose-dependent manner; inhibition of binding was also observed in chick bone cells. The effects of CsA on osteoclast viability and resorptive function may be due to a direct effect on the osteoclasts and/or to an interaction with the nonosteoclastic cell population in the culture.
我们研究了环孢素A(CsA)对鸡长骨细胞24小时培养中破骨细胞介导的基础骨吸收以及牛甲状旁腺激素(1-34)(bPTH)刺激的骨吸收的影响。在高浓度(10微克/毫升)时,CsA对培养中的破骨细胞和单核细胞均具有细胞毒性作用。在1微克/毫升时,CsA抑制基础和bPTH刺激的骨吸收,但在24小时内无细胞毒性。我们还研究了bPTH与成骨细胞系Saos-2以及悬浮培养的鸡长骨细胞的结合。CsA以剂量依赖性方式抑制Saos-2中bPTH的结合;在鸡骨细胞中也观察到结合受到抑制。CsA对破骨细胞活力和吸收功能的影响可能是由于对破骨细胞的直接作用和/或与培养中非破骨细胞群体的相互作用。