TY - JOUR
T1 - Gene expression profiles in rat liver treated with perfluorooctanoic acid (PFOA)
AU - Guruge, Keerthi S.
AU - Yeung, Leo W.Y.
AU - Yamanaka, Noriko
AU - Miyazaki, Shigeru
AU - Lam, Paul K.S.
AU - Giesy, John P.
AU - Jones, Paul D.
AU - Yamashita, Nobuyoshi
N1 - Funding Information:
This research work was partially supported from the Japanese Ministry of Environment under the Global Environment Conservation Research Fund (2004–2008) to K.S.G. and by a CERG grant (CityU1401/05M) from the Hong Kong Research Grants Council awarded to P.K.S.L. The authors also thank Dr. H. Hoshiba and animal care members of NIAH for their invaluable assistance during the study. Conflict of interest: none declared.
PY - 2006/1
Y1 - 2006/1
N2 - Perfluorooctanoic acid (PFOA; Pentadecafluorooctanoic acid) is widely used in various industrial applications. It is persistent in the environment and does not appear to undergo further degradation or transformation. PFOA is found in tissues including blood of wildlife and humans; however, the environmental fate and biological effects of PFOA remain unclear. Microarray techniques of gene expression have become a powerful approach for exploring the biological effects of chemicals. Here, the Affymetrix, Inc. rat genome 230 2.0 GeneChip was used to identify alterations in gene regulation in Sprague-Dawley rats treated with five different concentrations of PFOA. Male rats were exposed by daily gavage to 1, 3, 5, 10, or 15 mg PFOA/kg, body weight (bw)/day for 21 days and at the end of the exposure, liver was isolated and total liver RNA were used for the gene chip analysis. Over 500 genes, whose expression was significantly (p < 0.0025) altered by PFOA at two-fold changes compared to control, were examined. The effects were dose-dependent with exposure to 10 mg PFOA/kg, bw/day, causing alteration in expression of the greatest number of genes (over 800). Approximately 106 genes and 38 genes were consistently up- or down-regulated, respectively, in all treatment groups. The largest categories of induced genes were those involved in transport and metabolism of lipids, particularly fatty acids. Other induced genes were involved in cell communication, adhesion, growth, apoptosis, hormone regulatory pathways, proteolysis and peptidolysis and signal transduction. The genes expression of which was suppressed were related to transport of lipids, inflammation and immunity, and especially cell adhesion. Several other genes involved in apoptosis; regulation of hormones; metabolism; and G-protein coupled receptor protein signaling pathways were significantly suppressed.
AB - Perfluorooctanoic acid (PFOA; Pentadecafluorooctanoic acid) is widely used in various industrial applications. It is persistent in the environment and does not appear to undergo further degradation or transformation. PFOA is found in tissues including blood of wildlife and humans; however, the environmental fate and biological effects of PFOA remain unclear. Microarray techniques of gene expression have become a powerful approach for exploring the biological effects of chemicals. Here, the Affymetrix, Inc. rat genome 230 2.0 GeneChip was used to identify alterations in gene regulation in Sprague-Dawley rats treated with five different concentrations of PFOA. Male rats were exposed by daily gavage to 1, 3, 5, 10, or 15 mg PFOA/kg, body weight (bw)/day for 21 days and at the end of the exposure, liver was isolated and total liver RNA were used for the gene chip analysis. Over 500 genes, whose expression was significantly (p < 0.0025) altered by PFOA at two-fold changes compared to control, were examined. The effects were dose-dependent with exposure to 10 mg PFOA/kg, bw/day, causing alteration in expression of the greatest number of genes (over 800). Approximately 106 genes and 38 genes were consistently up- or down-regulated, respectively, in all treatment groups. The largest categories of induced genes were those involved in transport and metabolism of lipids, particularly fatty acids. Other induced genes were involved in cell communication, adhesion, growth, apoptosis, hormone regulatory pathways, proteolysis and peptidolysis and signal transduction. The genes expression of which was suppressed were related to transport of lipids, inflammation and immunity, and especially cell adhesion. Several other genes involved in apoptosis; regulation of hormones; metabolism; and G-protein coupled receptor protein signaling pathways were significantly suppressed.
KW - Fatty acid and lipid metabolism
KW - GeneChip
KW - Liver gene expression
KW - PFOA
KW - Perfluorinated compounds
UR - http://www.scopus.com/inward/record.url?scp=29544437778&partnerID=8YFLogxK
U2 - 10.1093/toxsci/kfj011
DO - 10.1093/toxsci/kfj011
M3 - Article
C2 - 16221955
AN - SCOPUS:29544437778
SN - 1096-6080
VL - 89
SP - 93
EP - 107
JO - Toxicological Sciences
JF - Toxicological Sciences
IS - 1
ER -