Reynolds E S
J Cell Biol. 1965 Jun;25(3):Suppl:53-75. doi: 10.1083/jcb.25.3.53.
Accumulation of calcium in the mitochondria of rat liver parenchymal cells at 16 and 24 hours after poisoning with carbon tetrachloride is associated with an increase in amount of liver inorganic phosphate, the persistence of mitochondrial adenosine triphosphatase activity, and the formation of electron-opaque intramitochondrial masses in cells with increased calcium contents. These masses, which form within the mitochondrial matrix adjacent to internal mitochondrial membranes, resemble those observed in isolated mitochondria which accumulate calcium and inorganic phosphate; are present in a locus similar to that of electron opacities which result from electron-histochemical determination of mitochondrial ATPase activity; and differ in both appearance and position from matrix granules of normal mitochondria. After poisoning, normal matrix granules disappear from mitochondria prior to their accumulation of calcium. As calcium-associated electron-opaque intramitochondrial masses increase in size, mitochondria degenerate in appearance. At the same time, cytoplasmic membrane systems of mid-zonal and centrilobular cells are disrupted by degranulation of the rough endoplasmic reticulum and the formation of labyrinthine tubular aggregates. The increase in amount of inorganic phosphate in rat liver following poisoning is balanced by a decreased amount of phosphoprotein. These chemical events do not appear to be related, however, as the inorganic phosphate accumulated is derived from serum inorganic phosphate.
四氯化碳中毒后16小时和24小时,大鼠肝实质细胞线粒体中钙的积累与肝脏无机磷酸盐含量的增加、线粒体三磷酸腺苷酶活性的持续存在以及钙含量增加的细胞中线粒体内部电子不透明物质的形成有关。这些物质在线粒体内膜附近的线粒体基质中形成,类似于在积累钙和无机磷酸盐的分离线粒体中观察到的物质;存在于与线粒体ATP酶活性的电子组织化学测定所产生的电子不透明区域相似的位置;在外观和位置上与正常线粒体的基质颗粒不同。中毒后,正常的基质颗粒在钙积累之前从线粒体中消失。随着与钙相关的线粒体内部电子不透明物质体积的增加,线粒体外观发生退化。与此同时,中区和小叶中心细胞的细胞质膜系统因粗面内质网的脱颗粒和迷宫状管状聚集体的形成而受到破坏。中毒后大鼠肝脏中无机磷酸盐含量的增加与磷蛋白含量的减少相平衡。然而,这些化学事件似乎没有关联,因为积累的无机磷酸盐来自血清无机磷酸盐。