McVicker Benita L, Tuma Dean J, Casey Carol A
Veterans Affairs Medical Center, Research Service (151), 4101 Woolworth Avenue, Omaha, NE 68105, USA.
World J Gastroenterol. 2007 Oct 7;13(37):4960-6. doi: 10.3748/wjg.v13.i37.4960.
Chronic ethanol consumption is associated with serious and potentially fatal alcohol-related liver injuries such as hepatomegaly, alcoholic hepatitis and cirrhosis. Moreover, it has been documented that the clinical progression of alcohol-induced liver damage may be associated with an increase in hepatocellular death that involves apoptotic mechanisms. Although much information has been learned about the clinical manifestations associated with alcohol-related diseases, the search continues for a better understanding of the molecular and/or cellular mechanisms by which ethanol exerts its deleterious effects such as the induction of pro-apoptotic mechanisms and related cell damaging events. As part of the effort to enhance our understanding of those particular cellular pathways and mechanisms associated with ethanol toxicity, researchers over the years have utilized a variety of model systems. Recently, work has come forth demonstrating the utility of a hybrid cell line (WIF-B) as a cell culture model system for the study of alcohol-associated alterations in hepatocellular mechanisms. Success with such emerging model systems could aid in the development of potential therapeutic treatments for the prevention of alcohol-induced apoptotic cell death that may ultimately serve as a significant target in delaying the onset and/or progression of clinical symptoms of alcohol-mediated liver disease. This review article summarizes the current understanding of ethanol-mediated modifications in cell survival and thus the promotion of pro-apoptotic events with emphasis on analyses made in various experimental model systems, particularly the more recently characterized WIF-B cell system.
长期饮酒与严重且可能致命的酒精相关肝损伤有关,如肝肿大、酒精性肝炎和肝硬化。此外,有文献记载,酒精性肝损伤的临床进展可能与涉及凋亡机制的肝细胞死亡增加有关。尽管我们已经了解了许多与酒精相关疾病的临床表现,但仍在继续探索,以更好地理解乙醇发挥其有害作用(如诱导促凋亡机制和相关细胞损伤事件)的分子和/或细胞机制。作为加强我们对与乙醇毒性相关的特定细胞途径和机制理解的努力的一部分,多年来研究人员使用了各种模型系统。最近,有研究表明一种杂交细胞系(WIF-B)作为一种细胞培养模型系统,可用于研究酒精相关的肝细胞机制改变。这种新兴模型系统的成功应用有助于开发潜在的治疗方法,以预防酒精诱导的凋亡性细胞死亡,这最终可能成为延缓酒精性肝病临床症状发作和/或进展的重要靶点。这篇综述文章总结了目前对乙醇介导的细胞存活修饰以及促凋亡事件促进作用的理解,重点是在各种实验模型系统中进行的分析,特别是最近表征的WIF-B细胞系统。