Snowdowne K W, Freudenrich C C, Borle A B
J Biol Chem. 1985 Sep 25;260(21):11619-26.
The effect of anoxia and substrate removal on cytosolic free calcium (Ca2+i), cell calcium, ATP content, and calcium efflux was determined in cultured monkey kidney cells (LLC-MK2) exposed to 95% N2, 5% CO2 for 60 min. In the control period, the basal Ca2+i level was 70.8 +/- 9.4 nM. During 1 h of anoxia without substrate, ATP content decreased 70%, Ca2+i and calcium efflux increased 2.5-fold, while the total cell calcium did not change. When the cells were perfused again with O2 and 5 mM glucose, the ATP concentration, Ca2+i, and calcium efflux returned to control levels within 15-20 min. In the presence of 20 mM glucose, anoxia did not produce any change in ATP, in Ca2+i or in calcium efflux. An important source of calcium contributing to the rise in Ca2+i induced by anoxia appears to be extracellular because the rate of rise in Ca2+i is proportional to the extracellular calcium concentration, and because La3+ which blocks calcium influx greatly reduces the rise in Ca2+i. Mitochondria appear to control Ca2+i as well since the early rise in Ca2+i cannot be blocked by La3+ during the initial phase of anoxia, and since the mitochondrial inhibitor carbonyl cyanide p-trifluoromethoxyphenylhydrazone increases Ca2+i further during reoxygenation and slows the return of Ca2+i to control levels.
在暴露于95% N₂、5% CO₂ 60分钟的培养猴肾细胞(LLC-MK2)中,测定了缺氧和底物去除对胞质游离钙(Ca²⁺i)、细胞钙、ATP含量及钙外流的影响。在对照期,基础Ca²⁺i水平为70.8±9.4 nM。在无底物的缺氧1小时期间,ATP含量下降70%,Ca²⁺i和钙外流增加2.5倍,而细胞总钙含量未改变。当细胞再次用O₂和5 mM葡萄糖灌注时,ATP浓度、Ca²⁺i和钙外流在15 - 20分钟内恢复到对照水平。在存在20 mM葡萄糖的情况下,缺氧对ATP、Ca²⁺i或钙外流均未产生任何变化。缺氧诱导Ca²⁺i升高的一个重要钙源似乎是细胞外的,因为Ca²⁺i的升高速率与细胞外钙浓度成正比,并且因为阻断钙内流的La³⁺大大降低了Ca²⁺i的升高。线粒体似乎也控制着Ca²⁺i,因为在缺氧初始阶段,Ca²⁺i的早期升高不能被La³⁺阻断,并且因为线粒体抑制剂羰基氰化物对三氟甲氧基苯腙在复氧期间进一步增加Ca²⁺i,并减缓Ca²⁺i恢复到对照水平的速度。