Cribb Alastair E, Peyrou Mathieu, Muruganandan Shanmugam, Schneider Laetitia
Laboratory of Comparative Pharmacogenetics, Department of Biomedical Sciences, Atlantic Veterinary College, University of Prince Edward Island, Charlottetown, PEI, Canada.
Drug Metab Rev. 2005;37(3):405-42. doi: 10.1080/03602530500205135.
The endoplasmic reticulum (ER) is involved in an array of cellular functions that play important roles in xenobiotic toxicity. The ER contains the majority of cytochrome P450 enzymes involved in xenobiotic metabolism, as well as a number of conjugating enzymes. In addition to its role in drug bioactivation and detoxification, the ER can be a target for damage by reactive intermediates leading to cell death or immune-mediated toxicity. The ER contains a set of luminal proteins referred to as ER stress proteins (including GRP78, GRP94, protein disulfide isomerase, and calreticulin). These proteins help regulate protein processing and folding of membrane and secretory proteins in the ER, calcium homeostasis, and ER-associated apoptotic pathways. They are induced in response to ER stress. This review discusses the importance of the ER in molecular events leading to cell death following xenobiotic exposure. Data showing that the ER is important in both renal and hepatic toxicity will be discussed.
内质网(ER)参与了一系列在异生物质毒性中起重要作用的细胞功能。内质网包含了大部分参与异生物质代谢的细胞色素P450酶以及许多结合酶。除了在药物生物活化和解毒方面的作用外,内质网可能成为反应性中间体损伤的靶点,从而导致细胞死亡或免疫介导的毒性。内质网含有一组被称为内质网应激蛋白的腔内蛋白(包括GRP78、GRP94、蛋白二硫键异构酶和钙网蛋白)。这些蛋白有助于调节内质网中膜蛋白和分泌蛋白的加工与折叠、钙稳态以及内质网相关的凋亡途径。它们在对内质网应激的反应中被诱导。本综述讨论了内质网在异生物质暴露后导致细胞死亡的分子事件中的重要性。将讨论表明内质网在肾毒性和肝毒性中均起重要作用的数据。