Yee J A, Sutton J K, Shew R L, Olansky L
J Cell Physiol. 1986 Aug;128(2):246-50. doi: 10.1002/jcp.1041280216.
The involvement of cAMP and calcium in the rise in alkaline phosphatase (AP) activity observed when confluent, serum-free primary cultures of neonatal mouse calvarial cells are treated with parathyroid hormone (PTH) has been studied. Synthetic bovine PTH [bPTH-(1-34)] increased cellular cAMP at concentrations (10(-9) to 10(-7) M) previously found to elevate AP activity. Other substances that increase cAMP in these cells (forskolin, prostaglandin E2, 8-bromoadenosine cAMP and 3-isobutyl-1-methylxanthine) also increased enzyme activity. By comparison, increasing the concentration of calcium in the culture medium from 1.8 to 3.8 or 5.8 mM lowered the magnitude of the maximal AP response. In addition, treatment of cultures with the divalent cation ionophore A23187 caused a significant decrease in AP activity. These results suggest that: 1) cAMP mediates the rise in the specific activity of AP in cultured neonatal mouse calvarial cells treated with bPTH-(1-34) and 2) the concentration of calcium in the environment significantly influences the responsivity of bone cells to the hormone.
研究了环磷酸腺苷(cAMP)和钙在新生小鼠颅骨细胞汇合、无血清原代培养物用甲状旁腺激素(PTH)处理时观察到的碱性磷酸酶(AP)活性升高过程中的作用。合成牛PTH [bPTH-(1-34)] 在先前发现可提高AP活性的浓度(10(-9)至10(-7) M)下增加细胞内cAMP。在这些细胞中增加cAMP的其他物质(福斯高林、前列腺素E2、8-溴腺苷cAMP和3-异丁基-1-甲基黄嘌呤)也增加了酶活性。相比之下,将培养基中钙的浓度从1.8 mM提高到3.8 mM或5.8 mM会降低最大AP反应的幅度。此外,用二价阳离子载体A23187处理培养物会导致AP活性显著降低。这些结果表明:1)cAMP介导了用bPTH-(1-34)处理的培养新生小鼠颅骨细胞中AP比活性的升高,2)环境中的钙浓度显著影响骨细胞对该激素的反应性。