Rao L G, March M, Murray T M
Division of Endocrinology and Metabolism, St. Michael's Hospital, Toronto, Ontario, Canada.
Bone Miner. 1989 Nov;7(3):191-204. doi: 10.1016/0169-6009(89)90077-9.
The calcium modulation of the cyclic 3',5'-adenosine monophosphate (cAMP) response to parathyroid hormone (PTH) was studied in a clonal osteosarcoma cell line ROS 17/2.8. CaCl2 was found to stimulate the PTH-sensitive cAMP response of intact cells. At the maximal concentration of 1 mM CaCl2, the maximum response to PTH was increased, but the ED50 for PTH and the time course of maximal cAMP production were not affected. Verapamil blunted, while the cation ionophore A23187 enhanced, the stimulatory effect of CaCl2. Trifluoperazine (TFP) and N-(6-aminohexyl-5-Cl-naphthalene sulfonamide) (W-7) inhibited the stimulatory effect of CaCl2. In membranes prepared in the presence of 0.1 mM CaCl2, a biphasic effect of CaCl2 was demonstrated: stimulation at concentrations of 60-100 microM, and an inhibition above 200 microM, when adenylate cyclase was assayed in the presence of 200 microM EGTA. Addition of exogenous calmodulin to membranes prepared in the presence of EGTA did not have any effect on the PTH-sensitive adenylate cyclase activity, suggesting that endogenous calmodulin was not effectively stripped from the membranes by EGTA treatment. It is concluded that Ca2+ has both a stimulatory and an inhibitory role in modulating PTH-sensitive adenylate cyclase in ROS 17/2.8 cells by as yet unknown mechanisms, and that the involvement of endogenous calmodulin is implicated.
在克隆骨肉瘤细胞系ROS 17/2.8中研究了钙对甲状旁腺激素(PTH)诱导的环3',5'-单磷酸腺苷(cAMP)反应的调节作用。发现氯化钙可刺激完整细胞对PTH敏感的cAMP反应。在氯化钙最大浓度为1 mM时,对PTH的最大反应增强,但PTH的半数有效浓度(ED50)和最大cAMP产生的时间进程未受影响。维拉帕米可减弱氯化钙的刺激作用,而阳离子载体A23187则增强该作用。三氟拉嗪(TFP)和N-(6-氨基己基-5-氯萘磺酰胺)(W-7)可抑制氯化钙的刺激作用。在含有0.1 mM氯化钙的条件下制备的细胞膜中,当在200 microM乙二醇双(2-氨基乙基醚)四乙酸(EGTA)存在下测定腺苷酸环化酶时,氯化钙呈现双相作用:在60 - 100 microM浓度下刺激,在200 microM以上抑制。向在EGTA存在下制备的细胞膜中添加外源性钙调蛋白对PTH敏感的腺苷酸环化酶活性没有任何影响,这表明EGTA处理未能有效去除细胞膜上的内源性钙调蛋白。结论是,Ca2+通过尚未明确的机制在调节ROS 17/2.8细胞中PTH敏感的腺苷酸环化酶方面兼具刺激和抑制作用,并且涉及内源性钙调蛋白。