Jongen J W, Willemstein-van Hove E C, van der Meer J M, Bos M P, Jüppner H, Segre G V, Abou-Samra A B, Feyen J H, Herrmann-Erlee M P
Laboratory of Cell Biology and Histology, University of Leiden, The Netherlands.
J Bone Miner Res. 1996 Sep;11(9):1218-25. doi: 10.1002/jbmr.5650110905.
We studied the effects of parathyroid hormone (PTH) on PTH parathyroid hormone related peptide (PTHrP) receptor mRNA level, PTHrP binding and PTH-stimulated cyclic adenosine monophosphate (cAMP) accumulation in osteoblasts, derived from fetal rat calvariae (ROB). Cells isolated during 10-70 minutes of collagenase treatment were seeded at a density of 25,000 cells/cm2 and cultured for 4 days. These cells show a fast increase in cAMP production after stimulation for 5 minutes with 20 nM bovine parathyroid hormone(1-34) (bPTH(1-34)). When ROB are incubated with bPTH(1-34) (0.04-40nM) for 24 h, a dose-dependent decrease of the PTH/PTHrP receptor mRNA level, PTHrP binding, and PTH-stimulated cAMP accumulation can be observed. Pretreatment of ROB with a high concentration of bPTH(1-34) (40 nM) leads within 15 minutes to a decrease in PTH-stimulated cAMP accumulation. However, it takes > or = 3 h before a significant decrease in PTH/PTHrP receptor mRNA level can be observed. Also a significant decrease in PTHrP binding is observed after only 4 h of incubation with bPTH(1-34). Compared with bPTH(1-34), pretreatment of ROB with bPTH(3-34) (40 and 100 nM) for 24 h causes smaller decreases in PTH-stimulated cAMP accumulation, PTHrP binding, and in the PTH/PTHrP receptor mRNA level. We investigated the possible involvement of the protein kinase A signaling pathway in the regulation of the PTH/PTHrP receptor mRNA expression. Both forskolin and (Bu)2cAMP decreased PTHrP binding and PTH/PTHrP mRNA levels. These observations suggest that chronic activation of the PKA signaling pathway may down-regulate PTH/PTHrP receptor expression and thus hormone responsiveness in "normal" osteoblasts. In short, we found that the decrease of the PTH-stimulated cAMP accumulation after long-term pretreatment with bPTH(1-34) is correlated with both PTH/PTHrP receptor mRNA level and PTHrP binding. These data also suggest that the initial desensitization (< 30 minutes) of PTH-stimulated cAMP responsiveness by pretreatment with a high concentration of bPTH(1-34) (40 nM) is not dependent on the number of available PTH/PTHrP receptors. The protein kinase A signaling pathway is involved in the regulation of the PTH/PTHrP receptor, but, regarding the effect of bPTH(3-34), other signaling systems are also involved.
我们研究了甲状旁腺激素(PTH)对源自胎鼠颅骨(ROB)的成骨细胞中PTH甲状旁腺激素相关肽(PTHrP)受体mRNA水平、PTHrP结合以及PTH刺激的环磷酸腺苷(cAMP)积累的影响。在胶原酶处理10 - 70分钟期间分离的细胞以25,000个细胞/cm²的密度接种,并培养4天。在用20 nM牛甲状旁腺激素(1 - 34)(bPTH(1 - 34))刺激5分钟后,这些细胞的cAMP产生迅速增加。当ROB与bPTH(1 - 34)(0.04 - 40 nM)孵育24小时时,可以观察到PTH/PTHrP受体mRNA水平、PTHrP结合以及PTH刺激的cAMP积累呈剂量依赖性下降。用高浓度的bPTH(1 - 34)(40 nM)对ROB进行预处理,15分钟内会导致PTH刺激的cAMP积累下降。然而,在可观察到PTH/PTHrP受体mRNA水平显著下降之前需要≥3小时。在用bPTH(1 - 34)孵育仅4小时后,也观察到PTHrP结合显著下降。与bPTH(1 - 34)相比,用bPTH(3 - 34)(40和100 nM)对ROB进行24小时预处理,导致PTH刺激的cAMP积累、PTHrP结合以及PTH/PTHrP受体mRNA水平的下降较小。我们研究了蛋白激酶A信号通路在PTH/PTHrP受体mRNA表达调节中的可能作用。福斯可林和(Bu)2cAMP均降低了PTHrP结合和PTH/PTHrP mRNA水平。这些观察结果表明,PKA信号通路的慢性激活可能下调PTH/PTHrP受体表达,从而降低“正常”成骨细胞中的激素反应性。简而言之,我们发现用bPTH(1 - 34)长期预处理后PTH刺激的cAMP积累的下降与PTH/PTHrP受体mRNA水平和PTHrP结合均相关。这些数据还表明,用高浓度的bPTH(1 - 34)(40 nM)预处理对PTH刺激的cAMP反应性的初始脱敏(<30分钟)不依赖于可用的PTH/PTHrP受体数量。蛋白激酶A信号通路参与PTH/PTHrP受体的调节,但就bPTH(3 - 34)的作用而言,其他信号系统也参与其中。