Stewart P J, Stern P H
Calcif Tissue Int. 1987 Jan;40(1):21-6. doi: 10.1007/BF02555724.
We have developed and characterized a new bone resorption system to test the effect of estrogen on vertebral bone in vitro. Neonatal mouse vertebral bones prelabeled with 45Ca were maintained in stationary tissue culture for 60-108 hours at 37 degrees C in 5% CO2/air. Each vertebral bone measured approximately 1 mm X 1 mm. Hormonal treatments were added directly to the incubation medium. The morphological appearance of these bones, before and after the onset of resorption, was examined by scanning electron microscopy. Bone resorption was measured by determining the % of the bone 45Ca released into the incubation medium. Vertebral bone resorption was stimulated in a dose-dependent manner by parathyroid hormone (1-100 nM), 1,25 dihydroxyvitamin D3 (0.0325-3.25 nM), and prostaglandin E2 (3-3000 nM). Epidermal growth factor (300 ng/ml) produced a small stimulation of bone resorption which was not inhibited by indomethacin (0.5 microM). Likewise, indomethacin (0.5 microM) did not inhibit PTH-stimulated vertebral bone resorption. Calcitonin (6.6 nM) produced a 79% inhibition of bone resorption induced by PTH (10 nM), whereas estradiol (up to 3 microM) did not inhibit bone resorption. Our results demonstrate that estrogen does not have a direct effect on vertebral bone tissue in vitro. This new bone culture system is a sensitive assay for the direct effects of resorptive agents on vertebral bone.
我们开发并鉴定了一种新的骨吸收系统,以在体外测试雌激素对椎骨的作用。预先用45Ca标记的新生小鼠椎骨在37℃、5%二氧化碳/空气环境下于静态组织培养中维持60 - 108小时。每块椎骨尺寸约为1毫米×1毫米。激素处理直接添加到孵育培养基中。通过扫描电子显微镜检查这些骨在吸收开始前后的形态外观。通过测定释放到孵育培养基中的骨45Ca百分比来测量骨吸收。甲状旁腺激素(1 - 100 nM)、1,25 - 二羟维生素D3(0.0325 - 3.25 nM)和前列腺素E2(3 - 3000 nM)以剂量依赖方式刺激椎骨吸收。表皮生长因子(300 ng/ml)对骨吸收有轻微刺激作用,且不受吲哚美辛(0.5 microM)抑制。同样,吲哚美辛(0.5 microM)也不抑制甲状旁腺激素刺激的椎骨吸收。降钙素(6.6 nM)可使甲状旁腺激素(10 nM)诱导的骨吸收抑制79%,而雌二醇(高达3 microM)不抑制骨吸收。我们的结果表明,雌激素在体外对椎骨组织没有直接作用。这种新的骨培养系统是一种用于检测吸收剂对椎骨直接作用的灵敏测定方法。