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细胞外钙浓度独立于HeLa细胞中肌醇1,4,5 - 三磷酸产生来控制细胞内钙闪烁的频率。

Extracellular calcium concentration controls the frequency of intracellular calcium spiking independently of inositol 1,4,5-trisphosphate production in HeLa cells.

作者信息

Bootman M D, Young K W, Young J M, Moreton R B, Berridge M J

机构信息

The Babraham Institute Laboratory of Molecular Signalling, Department of Zoology, University of Cambridge, U.K.

出版信息

Biochem J. 1996 Feb 15;314 ( Pt 1)(Pt 1):347-54. doi: 10.1042/bj3140347.

Abstract

Stimulation of single HeLa cells with histamine evoked repetitive increases of the intracellular calcium ion concentration (Ca2+ spikes). The frequency of Ca2+ spiking increased as the extracellular hormone concentration was elevated. In addition, the frequency of Ca2+ spiking could be accelerated by increasing the extracellular Ca2+ concentration ([Ca2+]0) in the presence of a constant hormone concentration. The range of [Ca2+]0 over which the spiking frequency could be titrated was nominally-zero to 10mM, being half-maximally effective at approx. 1 and 2.5mM for 37 and 22 degrees C respectively. The effect of [Ca2+]0 on inositol phosphates production was also examined. Changes of [Ca2+]0 over a range which had been found to affect the frequency of Ca2+ spiking did not have any effect on the rate of myo-inositol 1,4,5-trisphosphate (InsP3) production, although an increase in inositol phosphates production was observed as [Ca2+]0 was increased from zero to values giving less than half-maximal Ca2+ spike frequency. These data suggest that at low Ca2+ spike frequency, Ca2+-stimulated activation of phospholipase C may contribute to Ca2+ spiking in HeLa cells, but under some conditions the availability of Ca2+ to the intracellular stores, rather than changes in the rate of InsP3 production, determines the Ca2+ spike frequency.

摘要

用组胺刺激单个海拉细胞会引起细胞内钙离子浓度的反复增加(钙离子尖峰)。随着细胞外激素浓度升高,钙离子尖峰的频率增加。此外,在激素浓度恒定的情况下,通过增加细胞外钙离子浓度([Ca2+]0)可加速钙离子尖峰的频率。能够对尖峰频率进行滴定的[Ca2+]0范围名义上为零至10mM,在37℃和22℃时分别约为1mM和2.5mM时达到最大效应的一半。还研究了[Ca2+]0对肌醇磷酸生成的影响。在已发现会影响钙离子尖峰频率的范围内改变[Ca2+]0,对肌醇-1,4,5-三磷酸(InsP3)的生成速率没有任何影响,尽管当[Ca2+]0从零增加到产生小于最大钙离子尖峰频率一半的值时,观察到肌醇磷酸生成增加。这些数据表明,在低钙离子尖峰频率下,钙离子刺激的磷脂酶C活化可能有助于海拉细胞中的钙离子尖峰,但在某些情况下,细胞内储存库可利用的钙离子而非InsP3生成速率的变化决定了钙离子尖峰频率。

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