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人类红细胞的细胞内钙含量:与钠转运系统的关系。

Intracellular calcium content of human erythrocytes: relation to sodium transport systems.

作者信息

Engelmann B, Duhm J

机构信息

Department of Physiology, University of Munich, Federal Republic of Germany.

出版信息

J Membr Biol. 1987;98(1):79-87. doi: 10.1007/BF01871047.

DOI:10.1007/BF01871047
PMID:2822934
Abstract

To study the possible role of intracellular Ca (Cai) in controlling the activities of the Na+-K+ pump, the Na+-K+ cotransport and the Na+/Li+ exchange system of human erythrocytes, a method was developed to measure the amount of Ca embodied within the red cell. For complete removal of Ca associated with the outer aspect of the membrane, it proved to be essential to wash the cells in buffers containing less than 20 nM Ca. Ca was extracted by HClO4 in Teflon vessels boiled in acid to avoid Ca contaminations and quantitated by flameless atomic absorption. Cai of fresh human erythrocytes of apparently healthy donors ranged between 0.9 and 2.8 mumol/liter cells. The mean value found in females was significantly higher than in males. The interindividual different Ca contents remained constant over periods of more than one year. Sixty to 90% of Cai could be removed by incubation of the cells with A23187 and EGTA. The activities of the Na+-K+ pump, of Na+-K+ cotransport and Na+/Li+ exchange and the mean cellular hemoglobin content fell with rising Cai; the red cell Na+ and K+ contents rose with Cai. Ca depletion by A23187 plus EGTA as well as chelation of intracellular Ca2+ by quin-2 did not significantly enhance the transport rates. It is concluded that the large scatter of the values of Cai of normal human erythrocytes reported in the literature mainly results from a widely differing removal of Ca associated with the outer aspect of the membrane.

摘要

为了研究细胞内钙(Cai)在控制人红细胞钠钾泵、钠钾协同转运和钠/锂交换系统活性方面的可能作用,开发了一种测量红细胞内钙含量的方法。为了完全去除与细胞膜外表面相关的钙,事实证明用含钙量低于20 nM的缓冲液洗涤细胞至关重要。钙在聚四氟乙烯容器中用高氯酸提取,容器在酸中煮沸以避免钙污染,并用无火焰原子吸收法定量。明显健康供体的新鲜人红细胞的Cai在0.9至2.8 μmol/升细胞之间。女性的平均值显著高于男性。个体间不同的钙含量在一年多的时间里保持不变。通过将细胞与A23187和乙二醇双四乙酸(EGTA)孵育,可以去除60%至90%的Cai。钠钾泵、钠钾协同转运和钠/锂交换的活性以及平均细胞血红蛋白含量随Cai升高而下降;红细胞钠和钾含量随Cai升高而升高。A23187加EGTA导致的钙耗竭以及quin-2对细胞内Ca2+的螯合并没有显著提高转运速率。得出的结论是,文献中报道的正常人红细胞Cai值的较大离散主要是由于与细胞膜外表面相关的钙去除差异很大。

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