Scutt A, Duvos C, Lauber J, Mayer H
Department of Genetics, Gesellschaft für Biotechnologische Forschung, Braunschweig, Germany.
Calcif Tissue Int. 1994 Sep;55(3):208-15. doi: 10.1007/BF00425877.
Both PGE2 and PTH (1-34) caused a time- and concentration-dependent stimulation of proliferation by embryonic chick periosteal cells. Cells were exposed to the agents for different periods of time, the medium was replaced with fresh medium, and 3H-TdR incorporation was measured after 16 hours. Challenge with 10(-6) M prostaglandin E2 (PGE2) or 10(-7) M parathyroid hormone (1-34) (PTH) for 5 minutes produced 4- and 5.5-fold increases in 3H-TdR incorporation, respectively. Longer exposures, however, produced diminishing responses and after 45 minutes, only minimal effects or slight inhibitions were seen. These time-dependent effects were also seen with forskolin and dibutyryl-cAMP; TPA on the other hand stimulated DNA synthesis after both short- and long-term exposure. Both PGE2 and PTH (1-34) stimulated cAMP synthesis in periosteal cells but neither could be shown to stimulate protein kinase-C (PKC) at concentrations required for stimulation of proliferation, and dibutyryl-cyclic AMP (cAMP) effectively inhibited endogenous PKC activity. It is possible that the stimulation of proliferation by short-term exposure to PGE2 and PTH (1-34) is mediated by cAMP and that the time dependency possibly stems from the inhibition of endogenous PKC activity by increased intracellular cAMP levels.
前列腺素E2(PGE2)和甲状旁腺激素(1-34)[PTH(1-34)]均能引起鸡胚骨膜细胞增殖的时间和浓度依赖性刺激。将细胞暴露于这些因子不同时间后,更换新鲜培养基,16小时后检测3H-胸腺嘧啶核苷(3H-TdR)掺入量。用10(-6)M前列腺素E2(PGE2)或10(-7)M甲状旁腺激素(1-34)[PTH(1-34)]刺激5分钟,3H-TdR掺入量分别增加4倍和5.5倍。然而,更长时间的暴露产生的反应逐渐减弱,45分钟后,仅见最小效应或轻微抑制。福斯高林和二丁酰环磷腺苷(dbcAMP)也有这种时间依赖性效应;另一方面,佛波酯(TPA)在短期和长期暴露后均能刺激DNA合成。PGE2和PTH(1-34)均能刺激骨膜细胞合成环磷腺苷(cAMP),但在刺激增殖所需的浓度下,二者均未显示能刺激蛋白激酶C(PKC),且二丁酰环磷腺苷(dbcAMP)能有效抑制内源性PKC活性。短期暴露于PGE2和PTH(1-34)对增殖的刺激可能是由cAMP介导的,而时间依赖性可能源于细胞内cAMP水平升高对内源性PKC活性的抑制。