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骨细胞克隆之间的电生理差异:对甲状旁腺激素的膜电位反应及与环磷酸腺苷反应的相关性。

Electrophysiological differences between bone cell clones: membrane potential responses to parathyroid hormone and correlation with the cAMP response.

作者信息

Ferrier J, Ward A

出版信息

J Cell Physiol. 1986 Feb;126(2):237-42. doi: 10.1002/jcp.1041260212.

Abstract

Electrophysiological measurements on three clonally derived bone cell populations showed a positive correlation between longer-term hyperpolarizing membrane potential responses to parathyroid hormone (PTH) and an intracellular cAMP response to PTH. One clone (RCJ 1.20) had no sustained electrophysiological response and no cAMP response to PTH. Another clone (ROS 17/2.8) had both a sustained hyperpolarizing response and a cAMP response to PTH. The third clone (RCB 2.2) initially had both an electrophysiological response and a cAMP response to PTH, but both responses were lost after prolonged growth in culture. Application of dibutyryl cAMP to RCJ 1.20 and ROS 17/2.8 cells produced both transient and sustained hyperpolarizing responses. Application of isobutylmethylxanthine produced a sustained hyperpolarization. These results suggest that the hyperpolarizing response to PTH is related to a cAMP-mediated increase in Ca2+ conductance, which leads to an increase in Ca2+-activated K+ conductance. The pronounced membrane potential spikes and fluctuations that occur in some of the clonal lines were shown to be unrelated to the hyperpolarizing response to PTH. This was demonstrated by the lack of correlation between the occurrence of the spikes or fluctuations and the occurrence of the hyperpolarizing response to PTH in the various cell lines, by the lack of effect of PTH on the spikes and fluctuations, and by the lack of effect on the hyperpolarizing response to PTH of verapamil and quinine, both of which significantly reduce the spikes and fluctuations.

摘要

对三个克隆衍生的骨细胞群体进行的电生理测量表明,对甲状旁腺激素(PTH)的长期超极化膜电位反应与对PTH的细胞内cAMP反应之间存在正相关。一个克隆(RCJ 1.20)对PTH没有持续的电生理反应,也没有cAMP反应。另一个克隆(ROS 17/2.8)对PTH既有持续的超极化反应,也有cAMP反应。第三个克隆(RCB 2.2)最初对PTH既有电生理反应,也有cAMP反应,但在培养中长时间生长后,这两种反应都消失了。将二丁酰cAMP应用于RCJ 1.20和ROS 17/2.8细胞,产生了瞬时和持续的超极化反应。应用异丁基甲基黄嘌呤产生了持续的超极化。这些结果表明,对PTH的超极化反应与cAMP介导的Ca2+电导增加有关,这导致Ca2+激活的K+电导增加。在一些克隆系中出现的明显膜电位尖峰和波动被证明与对PTH的超极化反应无关。这通过各种细胞系中尖峰或波动的发生与对PTH的超极化反应的发生之间缺乏相关性、PTH对尖峰和波动缺乏影响以及维拉帕米和奎宁对PTH的超极化反应缺乏影响得到证明,这两种药物都能显著减少尖峰和波动。

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