Murphy E, Jacob R, Lieberman M
J Mol Cell Cardiol. 1985 Mar;17(3):221-31. doi: 10.1016/s0022-2828(85)80005-5.
The role of cytosolic free Ca2+ (Caf) in cell injury was investigated using two methods for measuring Caf in freshly disaggregated embryonic chick heart cells. The null-point method, using arsenazo III, is based on determining the extracellular Ca2+ concentration at which no net Ca2+ movement occurs when plasma membrane permeability is increased. With this technique, the null point Caf averaged 0.23 +/- 0.07 microM (n = 6) in the basal state. Using quin2, an intracellular fluorescent dye, to measure Caf a value of 0.05 +/- 0.01 microM (n = 5) was obtained. Elevation of Caf by various agents was associated with an increase in cell injury as measured by the release of the cytosolic enzyme, LDH. However, the relationship between Caf and LDH release was not a direct one under all experimental conditions, indicating that the level of Caf is not the sole determinant of cell injury.
利用两种测量刚分离的胚胎鸡心脏细胞胞质游离钙离子(Caf)的方法,研究了胞质游离钙离子在细胞损伤中的作用。使用偶氮胂III的零点法,是基于确定当质膜通透性增加时,没有净钙离子移动发生时的细胞外钙离子浓度。采用该技术,基础状态下的零点Caf平均为0.23±0.07微摩尔(n = 6)。使用细胞内荧光染料喹啉-2测量Caf,得到的值为0.05±0.01微摩尔(n = 5)。通过各种试剂使Caf升高与细胞损伤增加相关,细胞损伤通过胞质酶乳酸脱氢酶(LDH)的释放来衡量。然而,在所有实验条件下,Caf与LDH释放之间的关系并非直接关系,这表明Caf水平不是细胞损伤的唯一决定因素。