Denton R M, McCormack J G
Am J Physiol. 1985 Dec;249(6 Pt 1):E543-54. doi: 10.1152/ajpendo.1985.249.6.E543.
Three key dehydrogenases in mammalian mitochondria have been found to be activated by Ca2+ with a half-maximal effect at approximately 1 microM. These are pyruvate dehydrogenase, NAD+-isocitrate dehydrogenase, and oxoglutarate dehydrogenase. Activation of these enzymes can also be demonstrated in intact coupled mitochondria when extra mitochondrial Ca2+ is increased in the range of concentrations (0.1 to 2 microM) generally considered to occur in the cytoplasm of normal cells. It is argued that the main role of the calcium transport system in mammalian mitochondria is to relay changes in cytoplasmic Ca2+ into the mitochondrial matrix. Hormones and other extracellular messengers which stimulate ATP-requiring processes such as secretion or muscle contraction through increasing the cytoplasmic concentration of Ca2+ could in this way also increase intramitochondrial oxidative metabolism and hence promote the replenishment of ATP. Recent evidence obtained with heart and liver preparations in support of this view is reviewed.
已发现哺乳动物线粒体中的三种关键脱氢酶可被Ca2+激活,在约1微摩尔浓度时达到最大效应的一半。这些酶是丙酮酸脱氢酶、NAD+-异柠檬酸脱氢酶和氧代戊二酸脱氢酶。当线粒体外Ca2+在通常认为在正常细胞细胞质中会出现的浓度范围(0.1至2微摩尔)内增加时,完整的偶联线粒体中也可证明这些酶的激活。有人认为,哺乳动物线粒体中钙转运系统的主要作用是将细胞质中Ca2+的变化传递到线粒体基质中。通过增加细胞质中Ca2+浓度来刺激诸如分泌或肌肉收缩等需要ATP的过程的激素和其他细胞外信使,也可以通过这种方式增加线粒体内的氧化代谢,从而促进ATP的补充。本文综述了最近从心脏和肝脏制剂中获得的支持这一观点的证据。