Lajeunesse D, Frondoza C, Schoffield B, Sacktor B
National Institutes of Health, National Institute on Aging, Francis Scott Key Medical Center, Baltimore, MD 21224.
J Bone Miner Res. 1990 Sep;5(9):915-22. doi: 10.1002/jbmr.5650050904.
The human osteosarcoma cell line MG-63 has been used to study the production of the bone-specific protein, osteocalcin. In the absence of any stimuli, MG-63 cells secreted very low levels of osteocalcin. The secretion of osteocalcin started after a lag time of 10-12 h upon 1,25-(OH)2D3 treatment. Osteocalcin secretion was measured at doses as low as 0.03 nM (fourfold increase, p less than 0.05), and this activity increased further with higher doses of 1,25-(OH)2D3 to reach a plateau at 50 nM. The secretion increased transiently from very low levels in sparse cell cultures to peak values in subconfluent cultures (+/- 40%), two- to threefold above values obtained for confluent cells. Values for confluent cells average 55.9 +/- 2.0 ng/ml protein per 48 h. A similar behavior is observed for 1,25-(OH)2D3 receptor concentration under similar experimental conditions. Bmax increased transiently from sparse to subconfluent cell cultures (40-60% confluent) and reached values 50% lower in confluent cells. However, the receptor affinity was not affected by cell density. MG-63 cells also possessed an alkaline phosphatase isoenzyme of the bone-liver-kidney type that was stimulated by 1,25-(OH)2D3 treatment (two- to threefold) and inhibited by parathyroid hormone (40 nM, -25%, p less than 0.025). PTH and PGE2 increased cAMP production in a dose-dependent manner, but the cells were irresponsive to salmon calcitonin. Basal and PTH-responsive cyclic AMP production were also modulated by cell density. Dexamethasone pretreatment (100 nM, 48 h) stimulated the PTH-dependent cAMP production but failed to influence the response to PGE2.(ABSTRACT TRUNCATED AT 250 WORDS)
人骨肉瘤细胞系MG-63已被用于研究骨特异性蛋白骨钙素的产生。在没有任何刺激的情况下,MG-63细胞分泌的骨钙素水平非常低。经1,25-(OH)₂D₃处理后,骨钙素的分泌在延迟10 - 12小时后开始。骨钙素分泌量在低至0.03 nM的剂量下即可检测到(增加四倍,p小于0.05),并且随着1,25-(OH)₂D₃剂量的增加,这种活性进一步增强,在50 nM时达到平台期。在稀疏细胞培养中,分泌量从极低水平短暂增加到亚汇合培养中的峰值(±40%),比亚汇合细胞的值高出两到三倍。汇合细胞的值平均为每48小时55.9±2.0 ng/ml蛋白质。在类似的实验条件下,1,25-(OH)₂D₃受体浓度也观察到类似的行为。Bmax从稀疏细胞培养到亚汇合细胞培养(汇合度40 - 60%)短暂增加,在汇合细胞中达到的值低50%。然而,受体亲和力不受细胞密度的影响。MG-63细胞还具有骨-肝-肾型碱性磷酸酶同工酶,其受到1,25-(OH)₂D₃处理的刺激(增加两到三倍),并受到甲状旁腺激素(40 nM,-25%,p小于0.025)的抑制。甲状旁腺激素(PTH)和前列腺素E₂(PGE₂)以剂量依赖的方式增加cAMP的产生,但细胞对鲑鱼降钙素无反应。基础和PTH反应性环磷酸腺苷(cAMP)的产生也受细胞密度调节。地塞米松预处理(100 nM,48小时)刺激了PTH依赖的cAMP产生,但未能影响对PGE₂的反应。(摘要截断于250字)