Chung Heekyoung, Hong Doo-Pyo, Kim Hyun-Jun, Jang Ki-Seok, Shin Dong-Mi, Ahn Joon-Ik, Lee Yong-Sung, Kong Gu
Department of Pathology, College of Medicine, Hanyang University, 17 Haengdang-dong, Seongdong-gu, Seoul 133-791, Korea.
Toxicol Appl Pharmacol. 2005 Nov 1;208(3):242-54. doi: 10.1016/j.taap.2005.03.002.
Global gene expression profile was analyzed by microarray analysis of rat liver RNA after chronic carbon tetrachloride (CCl(4)) administration. Rats received 0.5 ml CCl(4)/kg three times a week, and the liver samples were obtained after 0, 30, 60, and 90 days of injection. Histopathologic studies of liver tissues enabled the classification of the CCl(4) effect into mild and severe fatty liver/steatosis (30 and 60 days, respectively) and fibrosis/cirrhosis (90 days) stages. The expression levels of 4,900 clones on a custom rat gene microarray were analyzed and the results were confirmed by semi-quantitative RT-PCR. Four hundred thirty-eight clones were differentially expressed with more than a 1.625-fold difference (which equals 0.7 in log2 scale) at one or more time points. Multiple genes involved in lipid metabolism and ribosome biogenesis showed differential transcript levels upon chronic CCl(4) administration, which was previously seen in acute rat model as well. In addition, a total of 149 clones were identified as fibrosis/cirrhosis-specific genes by either fold changes or Significance Analysis of Microarrays. In conclusion, we report microarray analysis results in rat liver upon chronic CCl(4) administration with a full chronological profile that not only covered fatty liver/steatosis but also later points of fibrosis/cirrhosis. These data will provide the insight of specific gene expression profiles that is implicated in the multistep process of fatty liver/steatosis and fibrosis/cirrhosis after chronic hepatotoxin exposure.
通过对慢性四氯化碳(CCl₄)给药后大鼠肝脏RNA进行微阵列分析,来分析全球基因表达谱。大鼠每周接受3次0.5 ml CCl₄/kg的剂量,在注射后0、30、60和90天获取肝脏样本。肝脏组织的组织病理学研究能够将CCl₄的影响分为轻度和重度脂肪肝/脂肪变性阶段(分别为30天和60天)以及纤维化/肝硬化阶段(90天)。分析了定制大鼠基因微阵列上4900个克隆的表达水平,并通过半定量RT-PCR对结果进行了确认。在一个或多个时间点,有438个克隆差异表达,差异倍数超过1.625倍(在log₂尺度上等于0.7)。慢性CCl₄给药后,多个参与脂质代谢和核糖体生物发生的基因显示出转录水平差异,这在急性大鼠模型中也有发现。此外,通过倍数变化或微阵列显著性分析,共鉴定出149个克隆为纤维化/肝硬化特异性基因。总之,我们报告了慢性CCl₄给药后大鼠肝脏的微阵列分析结果,具有完整的时间顺序谱,不仅涵盖了脂肪肝/脂肪变性,还包括了纤维化/肝硬化的后期阶段。这些数据将提供特定基因表达谱的见解,这些表达谱与慢性肝毒素暴露后脂肪肝/脂肪变性和纤维化/肝硬化的多步骤过程有关。