Becker G L
Biochim Biophys Acta. 1980 Jul 8;591(2):234-9. doi: 10.1016/0005-2728(80)90155-3.
An electrode-based system capable of monitoring ionized Ca2+ concentrations ([Ca2+]) < 1 microM was used to examine the regulation of extramitochondrial [Ca2+] by rat liver mitochondria. At the point of steady state balance between Ca2+ uptake and release, [Ca2+] ranged between 0.5 and 1.0 microM in a KCl/Hepes/succinate medium. When 1 mM Mg2+ was included in this basal medium, the range of steady state [Ca2+] values was 1-2 microM. Further additions (3 mM MgATP and 2 mM Pi) lowered extramitochondrial [Ca2+] to 0.4-0.8 microM. Thus under experimental conditions simulating the control of cytosolic [Ca2+], liver mitochondria buffered extramitochondrial [Ca2+] at constant values within the range of [Ca2+] estimated for liver cytosol; and cytosolic levels of Mg2+ and ATP significantly affected those steady state [Ca2+] values in directions consistent with previously reported effects of those modulators on mitochondrial Ca2+ uptake and release.
使用一种能够监测离子化Ca2+浓度([Ca2+])<1微摩尔的基于电极的系统,来研究大鼠肝脏线粒体对线粒体外[Ca2+]的调节作用。在Ca2+摄取与释放达到稳态平衡时,在KCl/HEPES/琥珀酸盐培养基中,[Ca2+]范围在0.5至1.0微摩尔之间。当在此基础培养基中加入1毫摩尔Mg2+时,稳态[Ca2+]值的范围为1 - 2微摩尔。进一步添加(3毫摩尔MgATP和2毫摩尔Pi)可使线粒体外[Ca2+]降至0.4 - 0.8微摩尔。因此,在模拟细胞质[Ca2+]调控的实验条件下,肝脏线粒体将线粒体外[Ca2+]缓冲在肝脏细胞质估计的[Ca2+]范围内的恒定值;并且细胞质中Mg2+和ATP的水平显著影响那些稳态[Ca2+]值,其影响方向与先前报道的这些调节剂对线粒体Ca2+摄取和释放的作用一致。