Cross-species Comparisons of Transcriptomic Alterations in Human and Rat Primary Hepatocytes Exposed to 2,3,7,8-Tetrachlorodibenzo-p-dioxin

被引:52
作者
Black, Michael B. [2 ]
Budinsky, Robert A. [1 ]
Dombkowski, Alan [3 ]
Cukovic, Daniela [3 ]
LeCluyse, Edward L. [4 ]
Ferguson, Stephen S. [4 ]
Thomas, Russell S. [2 ]
Rowlands, J. Craig [1 ]
机构
[1] Dow Chem Co USA, Toxicol & Environm Res & Consulting, Midland, MI 48674 USA
[2] Hamner Inst Hlth Sci, Res Triangle Pk, NC 27709 USA
[3] Wayne State Univ, Sch Med, Inst Environm Hlth Sci, Detroit, MI 48201 USA
[4] CellzDirectlInvitrogen, Durham, NC 27703 USA
关键词
aryl hydrocarbon receptor; dioxin; gene expression; human hepatocyte; rat hepatocyte; risk assessment; ARYL-HYDROCARBON RECEPTOR; SPRAGUE-DAWLEY RATS; HALOGENATED AROMATIC-HYDROCARBONS; ABNORMAL LIVER DEVELOPMENT; CELL-CYCLE PROGRESSION; HEPATIC STELLATE CELLS; DYNAMIC ORGAN-CULTURE; IN-VITRO MODEL; AH RECEPTOR; RISK-ASSESSMENT;
D O I
10.1093/toxsci/kfs069
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
A toxicogenomics approach was used to qualitatively and quantitatively compare the gene expression changes in human and rat primary hepatocytes exposed to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Hepatocytes from five individual rats and five individual humans were exposed for 24 h to 11 concentrations of TCDD ranging from 0.00001 to 100nM and a vehicle control. Gene expression changes were analyzed using whole-genome microarrays containing 13,002 orthologs. Significant changes in expression of individual orthologs at any concentration (fold change [FC] +/- 1.5 and false discovery rate < 0.05) were higher in the rat (1547) compared with human hepatocytes (475). Only 158 differentially expressed orthologs were common between rats and humans. Enrichment analysis was performed on the differentially expressed orthologs in each species with 49 and 34 enriched human and rat pathways, respectively. Only 12 enriched pathways were shared between the two species. The results demonstrate significant cross-species differences in expression at both the gene and pathway level. Benchmark dose analysis of gene expression changes showed an average 18-fold cross-species difference in potency among differentially expressed orthologs with the rat more sensitive than the human. Similar cross-species differences in potency were observed for signaling pathways. Using the maximum FC in gene expression as a measure of efficacy, the human hepatocytes showed on average a 20% lower efficacy among the individual orthologs showing differential expression. The results provide evidence for divergent cross-species gene expression changes in response to TCDD and are consistent with epidemiological and clinical evidence showing humans to be less sensitive to TCDD-induced hepatotoxicity.
引用
收藏
页码:199 / 215
页数:17
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