首页> 美国卫生研究院文献>Biochemical Journal >Extracellular calcium concentration controls the frequency of intracellular calcium spiking independently of inositol 145-trisphosphate production in HeLa cells.
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Extracellular calcium concentration controls the frequency of intracellular calcium spiking independently of inositol 145-trisphosphate production in HeLa cells.

机译:细胞外钙浓度独立于HeLa细胞中肌醇145-三磷酸的产生而控制细胞内钙突增的频率。

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摘要

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.
机译:用组胺刺激单个HeLa细胞会引起细胞内钙离子浓度(Ca2 +峰值)的重复增加。随着细胞外激素浓度的升高,Ca2 +掺入的频率增加。此外,在恒定激素浓度下,可通过增加细胞外Ca2 +浓度([Ca2 +] 0)来加快Ca2 +掺入的频率。可以确定尖峰频率的[Ca2 +] 0范围名义上为零至10mM,大约在10mM时有效。在37和22摄氏度下分别为1和2.5mM。还检查了[Ca 2+] 0对肌醇磷酸酯生产的影响。 [Ca2 +] 0在一定范围内的变化会影响钙离子加标的频率,尽管肌醇磷酸酯的增加,但对肌醇1,4,5-三磷酸酯(InsP3)的生成速率没有任何影响。当[Ca2 +] 0从零增加到给出小于最大Ca2 +尖峰频率一半的值时,观察到产生。这些数据表明,在低Ca2 +尖峰频率下,Ca2 +刺激的磷脂酶C的激活可能有助于HeLa细胞中Ca2 +的突增,但在某些情况下,Ca2 +在细胞内存储区的可用性而不是InsP3产生速率的变化决定了Ca2 +尖峰频率。

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