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通透化大鼠肠上皮细胞中ATP依赖的Ca2+摄取动力学。肌醇1,4,5-三磷酸的作用。

Kinetics of ATP-dependent Ca2+ uptake by permeabilized rat enterocytes. Effects of inositol 1,4,5-trisphosphate.

作者信息

van Corven E J, Verbost P M, de Jong M D, van Os C H

出版信息

Cell Calcium. 1987 Jun;8(3):197-206. doi: 10.1016/0143-4160(87)90018-2.

Abstract

Isolated rat enterocytes were permeabilized by saponin treatment. 45Ca2+ was accumulated by these cells when provided with ATP in a medium containing Ca2+ ligands. The use of oxalate, vanadate and mitochondrial inhibitors indicated that both non-mitochondrial and mitochondrial pools are involved. Kinetic analysis of non-mitochondrial Ca2+ uptake revealed a Km of 0.1 microM Ca2+ and a Vmax of 0.4 nmol Ca2+/mg protein X min for this Ca2+-pumping ATPase activity. Mitochondria started to take up Ca2+ between 0.2 and 0.3 microM free Ca2+ reaching maximal rates around 2 microM. At 1 microM free Ca2+ mitochondria accumulated 20 times more Ca2+ than the non-mitochondrial pool. Inositol 1,4,5-trisphosphate released 40% of the Ca2+ content of the non-mitochondrial pool. Half-maximal release was observed at 0.5 and 1.5 microM IP3 in duodenal and ileal cells respectively. These findings support the possibility that the phosphatidyl inositide metabolism plays a role in regulation of electrolyte transport in enterocytes.

摘要

通过皂素处理使分离的大鼠肠上皮细胞透化。当在含有钙离子配体的培养基中提供ATP时,这些细胞积累了45Ca2+。草酸盐、钒酸盐和线粒体抑制剂的使用表明,非线粒体池和线粒体池都参与其中。非线粒体Ca2+摄取的动力学分析显示,这种Ca2+泵ATP酶活性的Km为0.1 microM Ca2+,Vmax为0.4 nmol Ca2+/mg蛋白质×分钟。线粒体在游离Ca2+浓度为0.2至0.3 microM之间开始摄取Ca2+,在约2 microM时达到最大速率。在游离Ca2+浓度为1 microM时,线粒体积累的Ca2+比非线粒体池多20倍。肌醇1,4,5-三磷酸释放了非线粒体池Ca2+含量的40%。在十二指肠和回肠细胞中,分别在0.5和1.5 microM IP3时观察到最大释放量的一半。这些发现支持磷脂酰肌醇代谢在肠上皮细胞电解质转运调节中起作用的可能性。

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