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在离子载体A23187存在的情况下,钙离子杀伤细胞机制中两个钙依赖步骤和一个钠依赖步骤的证据。

Evidence for two calcium-dependent steps and a sodium-dependent step in the mechanism of cell killing by calcium ions in the presence of ionophore A23187.

作者信息

Shier W T, Dubourdieu D J

出版信息

Am J Pathol. 1985 Aug;120(2):304-15.

Abstract

Elevated intracellular Ca2+ appears to play an important role in the mechanism of cell killing in certain pathologic states such as ischemia. The authors have examined aspects of the biochemical mechanism of cell killing by elevated intracellular Ca2+ using as a model system cultured fibroblasts treated with ionophore A23187 in Ca2+-containing medium. Evidence has been obtained for two Ca2+-mediated steps and a Na+-mediated step in the cell killing process. The first Ca2+-mediated step occurs in low extracellular Ca2+ concentrations (1-100 microM) and exhibits a variety of characteristics in common with the arachidonic acid release response stimulated under the same conditions. These results are consistent with the arachidonic acid release response constituting or closely monitoring the initial injury process. The second Ca2+-mediated process is achieved at near physiologic extracellular Ca2+ concentrations in the absence of A23187. Killing of cells injured by the two Ca2+-dependent steps requires extracellular Na+ ions at half or more the physiologic concentration.

摘要

细胞内钙离子浓度升高似乎在某些病理状态(如缺血)下的细胞杀伤机制中发挥重要作用。作者以在含钙培养基中用离子载体A23187处理的培养成纤维细胞为模型系统,研究了细胞内钙离子浓度升高导致细胞杀伤的生化机制。已获得证据表明,在细胞杀伤过程中有两个钙介导步骤和一个钠介导步骤。第一个钙介导步骤发生在细胞外低钙浓度(1 - 100微摩尔)下,并且表现出与在相同条件下刺激的花生四烯酸释放反应有多种共同特征。这些结果与花生四烯酸释放反应构成或密切监测初始损伤过程一致。第二个钙介导过程是在生理细胞外钙浓度附近且不存在A23187的情况下实现的。由这两个钙依赖性步骤损伤的细胞杀伤需要细胞外钠离子浓度达到生理浓度的一半或更高。

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Role of lipid metabolism in cell killing by calcium plus ionophore A23187.
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本文引用的文献

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The role of calcium in cell death.钙在细胞死亡中的作用。
Life Sci. 1981 Sep 28;29(13):1289-95. doi: 10.1016/0024-3205(81)90670-6.
10
Role of phospholipid hydrolysis in the mechanism of toxic cell death by calcium and ionophore A23187.
Biochem Biophys Res Commun. 1982 Nov 16;109(1):106-12. doi: 10.1016/0006-291x(82)91572-8.

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