Suppr超能文献

纤细裸藻线粒体中钙离子转运的特性研究

Characterization of Ca2+ transport in Euglena gracilis mitochondria.

作者信息

Uribe A, Chávez E, Jiménez M, Zazueta C, Moreno-Sánchez R

机构信息

Departamento de Bioquímica, Instituto Nacional de Cardiología, México D.F., Mexico.

出版信息

Biochim Biophys Acta. 1994 Jun 28;1186(1-2):107-16. doi: 10.1016/0005-2728(94)90141-4.

Abstract

The present study was designed to establish the characteristics of the Ca2+ fluxes in isolated mitochondria of the protist Euglena gracilis. Uptake of Ca2+ and Sr2+ was supported by succinate and lactate oxidation. Ca2+ influx was slightly inhibited by 5 microM Ruthenium red and completely blocked by La3+ with a half-maximal inhibition attained at 50 microM. The addition of inorganic phosphate induced a 3-fold stimulation of Ca2+ uptake. Ca2+ uptake was inhibited by Mg2+ only in the absence of phosphate. Ca2+ efflux was induced by Na+, Li+ and K+ through a diltiazem-insensitive reaction. Ca2+ release, collapse of membrane potential and swelling were induced by Hg2+ and Cd2+ but not by carboxyatractyloside; cyclosporin A did not prevent the Ca2+ release induced by the heavy metal ions. Ca2+ uptake was achieved in the presence of 3 microM antimycin or 0.1 mM cyanide; this finding indicates that the alternative respiratory chain present in Euglena mitochondria can support this energy-dependent reaction. The data obtained suggest similar pathways, but different regulatory mechanisms, for Ca2+ transport between protist and mammalian mitochondria.

摘要

本研究旨在确定原生生物纤细裸藻分离线粒体中Ca2+通量的特征。琥珀酸和乳酸氧化支持Ca2+和Sr2+的摄取。5 microM钌红轻微抑制Ca2+内流,La3+完全阻断Ca2+内流,在50 microM时达到半数最大抑制。添加无机磷酸盐可使Ca2+摄取增加3倍。仅在无磷酸盐时,Mg2+抑制Ca2+摄取。Na+、Li+和K+通过地尔硫䓬不敏感反应诱导Ca2+外流。Hg2+和Cd2+诱导Ca2+释放、膜电位崩溃和肿胀,但羧基苍术苷不诱导;环孢素A不能阻止重金属离子诱导的Ca2+释放。在存在3 microM抗霉素或0.1 mM氰化物的情况下实现Ca2+摄取;这一发现表明纤细裸藻线粒体中存在的交替呼吸链可以支持这种能量依赖反应。获得的数据表明,原生生物和哺乳动物线粒体之间Ca2+转运的途径相似,但调节机制不同。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验