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PC12细胞中分泌与容量性钙内流的功能偶联

Functional coupling of secretion and capacitative calcium entry in PC12 cells.

作者信息

Koizumi S, Inoue K

机构信息

Division of Pharmacology, National Institute of Health Sciences, Tokyo, Japan.

出版信息

Biochem Biophys Res Commun. 1998 Mar 6;244(1):293-7. doi: 10.1006/bbrc.1998.8251.

Abstract

The caffeine-evoked effects on the intracellular Ca2+ concentration ([Ca2+]i) and on the release of dopamine by PC12 cells were investigated. Stimulation by caffeine resulted in a transient Ca2+ release which was followed by a sustained phase of Ca2+ entry through a non-voltage dependent pathway. Treatment with cyclopiazonic acid (CPA) or thapsigargin, inhibitors of the Ca2+ ATPase pump of the endoplasmic reticulum, resulted in only a sustained rise in [Ca2+]i in the presence of extracellular Ca2+. Pretreatment of cells with CPA or thapsigargin abolished the subsequent Ca2+ responses to caffeine. Caffeine also evoked the release of dopamine from the cells only in the presence of extracellular Ca2+, which was mimicked by CPA. These results suggest that store-dependent Ca2+ entry evoked by caffeine has an indispensable role in the secretory response in an excitable cell line, PC12 cells.

摘要

研究了咖啡因对PC12细胞内钙离子浓度([Ca2+]i)以及多巴胺释放的影响。咖啡因刺激导致钙离子短暂释放,随后通过非电压依赖性途径持续进入钙离子。用内质网钙离子ATP酶泵抑制剂环匹阿尼酸(CPA)或毒胡萝卜素处理,仅在细胞外存在钙离子的情况下导致[Ca2+]i持续升高。用CPA或毒胡萝卜素预处理细胞可消除随后对咖啡因的钙离子反应。咖啡因也仅在细胞外存在钙离子的情况下引起细胞释放多巴胺,这一作用可被CPA模拟。这些结果表明,咖啡因引发的储存依赖性钙离子内流在可兴奋细胞系PC12细胞的分泌反应中起不可或缺的作用。

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