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AhR 介导的 TCDD 诱导人肝成体干细胞基因表达的比较分析。

Comparative analysis of AhR-mediated TCDD-elicited gene expression in human liver adult stem cells.

机构信息

Department of Biochemistry & Molecular Biology, 501 Biochemistry Building, Wilson Road, East Lansing, MI 48824-1319, USA.

出版信息

Toxicol Sci. 2009 Nov;112(1):229-44. doi: 10.1093/toxsci/kfp189. Epub 2009 Aug 14.

Abstract

Time course and dose-response studies were conducted in HL1-1 cells, a human liver cell line with stem cell-like characteristics, to assess the differential gene expression elicited by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) compared with other established models. Cells were treated with 0.001, 0.01, 0.1, 1, 10, or 100nM TCDD or dimethyl sulfoxide vehicle control for 12 h for the dose-response study, or with 10nM TCDD or vehicle for 1, 2, 4, 8, 12, 24, or 48 h for the time course study. Elicited changes were monitored using a human cDNA microarray with 6995 represented genes. Empirical Bayes analysis identified 144 genes differentially expressed at one or more time points following treatment. Most genes exhibited dose-dependent responses including CYP1A1, CYP1B1, ALDH1A3, and SLC7A5 genes. Comparative analysis of HL1-1 differential gene expression to human HepG2 data identified 74 genes with comparable temporal expression profiles including 12 putative primary responses. HL1-1-specific changes were related to lipid metabolism and immune responses, consistent with effects elicited in vivo. Furthermore, comparative analysis of HL1-1 cells with mouse Hepa1c1c7 hepatoma cell lines and C57BL/6 hepatic tissue identified 18 and 32 commonly regulated orthologous genes, respectively, with functions associated with signal transduction, transcriptional regulation, metabolism and transport. Although some common pathways are affected, the results suggest that TCDD elicits species- and model-specific gene expression profiles.

摘要

时间进程和剂量反应研究在 HL1-1 细胞中进行,HL1-1 细胞是一种具有干细胞样特征的人肝细胞系,用于评估 2,3,7,8-四氯二苯并对二恶英(TCDD)与其他已建立模型相比引起的差异基因表达。细胞用 0.001、0.01、0.1、1、10 或 100nM TCDD 或二甲基亚砜载体对照处理 12 小时进行剂量反应研究,或用 10nM TCDD 或载体处理 1、2、4、8、12、24 或 48 小时进行时间进程研究。使用代表 6995 个基因的人类 cDNA 微阵列监测引起的变化。经验贝叶斯分析鉴定出 144 个在处理后一个或多个时间点差异表达的基因。大多数基因表现出剂量依赖性反应,包括 CYP1A1、CYP1B1、ALDH1A3 和 SLC7A5 基因。HL1-1 差异基因表达与人类 HepG2 数据的比较分析确定了 74 个具有相似时间表达谱的基因,包括 12 个推定的主要反应。HL1-1 特异性变化与脂质代谢和免疫反应有关,与体内诱导的作用一致。此外,HL1-1 细胞与小鼠 Hepa1c1c7 肝癌细胞系和 C57BL/6 肝组织的比较分析分别确定了 18 和 32 个共同调节的同源基因,这些基因的功能与信号转导、转录调控、代谢和转运有关。尽管一些共同途径受到影响,但结果表明 TCDD 引起物种和模型特异性基因表达谱。

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