Farber J L, El-Mofty S K
Am J Pathol. 1975 Oct;81(1):237-50.
Cell death and necrosis are important reactions of liver cells to injury that play a role in a wide variety of human liver diseases. A review is given of the important facets known about the biochemical basis of toxic liver cell death. Liver cells can withstand a great many specific biochemical and morphologic changes without loss of viability. Disturbances in RNA and protein synthesis, mitochondrial function, or release of lysosomal enzymes do not play a primary causative role in cell death. Many previous studies have tended to implicate the plasma membrane and its presumed role in maintaining the proper Ca2+ balance as the primary site of the development of irreversible hepatocyte damage. These studies have generally faced a major difficulty in determining if the observed changes are the cause or an effect of cell death. Galactosamine-induced liver cell injury seems to offer a potentially analyzable model for the experimental analysis of liver cell necrosis. Our studies on the role of plasma membrane injury and associated increases in total cellular calcium are reviewed, and a tentative working hypothesis for the pathogenesis of galactosamine-induced liver cell necrosis is presented.
细胞死亡和坏死是肝细胞对损伤的重要反应,在多种人类肝脏疾病中起作用。本文综述了关于毒性肝细胞死亡生化基础的已知重要方面。肝细胞能够承受许多特定的生化和形态学变化而不丧失活力。RNA和蛋白质合成、线粒体功能或溶酶体酶释放的紊乱在细胞死亡中并不起主要的致病作用。许多先前的研究倾向于认为质膜及其在维持适当钙平衡中的假定作用是不可逆肝细胞损伤发生的主要部位。这些研究在确定观察到的变化是细胞死亡的原因还是结果时通常面临一个主要困难。半乳糖胺诱导的肝细胞损伤似乎为肝细胞坏死的实验分析提供了一个潜在可分析的模型。我们对质膜损伤作用及细胞总钙含量相关增加的研究进行了综述,并提出了半乳糖胺诱导肝细胞坏死发病机制的初步工作假说。