ToxSci Advance Access originally published online on October 12, 2005
Toxicological Sciences 2006 89(1):93-107; doi:10.1093/toxsci/kfj011
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Gene Expression Profiles in Rat Liver Treated With Perfluorooctanoic Acid (PFOA)
,
* Toxico-Biochemistry Section, National Institute of Animal Health, Kannondai 3-1-5, Tsukuba, Ibaraki 305-0856, Japan; Department of Biology and Chemistry, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong SAR, PR China; Zoology Dept., National Food Safety and Toxicology Center and Center for Integrative Toxicology, Michigan State University, East Lansing, Michigan 48824; and Environmental Measurement Group, National Institute of Advance Industrial Science and Technology, Onogawa 16-1, Tsukuba, Ibaraki 305-8569, Japan
Received July 26, 2005; accepted September 22, 2005
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.
Key Words: perfluorinated compounds; PFOA; GeneChip; liver gene expression; fatty acid and lipid metabolism.
CiteULike 
Connotea 
Del.icio.us What's this?
This article has been cited by other articles:
|
|
 |
|
  N. J. Hickey, D. Crump, S. P. Jones, and S. W. Kennedy Effects of 18 Perfluoroalkyl Compounds on mRNA Expression in Chicken Embryo Hepatocyte Cultures Toxicol. Sci., October 1, 2009; 111(2): 311 - 320. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
J. A. Bjork and K. B. Wallace Structure-Activity Relationships and Human Relevance for Perfluoroalkyl Acid-Induced Transcriptional Activation of Peroxisome Proliferation in Liver Cell Cultures Toxicol. Sci., September 1, 2009; 111(1): 89 - 99. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
X. Cheng and C. D. Klaassen Critical Role of PPAR-{alpha} in Perfluorooctanoic Acid- and Perfluorodecanoic Acid-Induced Downregulation of Oatp Uptake Transporters in Mouse Livers Toxicol. Sci., November 1, 2008; 106(1): 37 - 45. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
K. P. Das, B. E. Grey, R. D. Zehr, C. R. Wood, J. L. Butenhoff, S.-C. Chang, D. J. Ehresman, Y.-M. Tan, and C. Lau Effects of Perfluorobutyrate Exposure during Pregnancy in the Mouse Toxicol. Sci., September 1, 2008; 105(1): 173 - 181. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 A. J. Nilsen, M. A. Landin, K. H. Haug, F. Fonnum, U. Berger, and H. Osmundsen Comparative hepatic gene expression profiling of rats treated with 1H,1H,2H,2H-heptadecafluorodecan-1-ol or with pentadecafluorooctanoic acid Physiol Genomics, August 1, 2008; 34(3): 285 - 303. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
M. M. Peden-Adams, J. M. Keller, J. G. EuDaly, J. Berger, G. S. Gilkeson, and D. E. Keil Suppression of Humoral Immunity in Mice following Exposure to Perfluorooctane Sulfonate Toxicol. Sci., July 1, 2008; 104(1): 144 - 154. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 M. B. Rosen, B. D. Abbott, D. C. Wolf, J. C. Corton, C. R. Wood, J. E. Schmid, K. P. Das, R. D. Zehr, E. T. Blair, and C. Lau Gene Profiling in the Livers of Wild-type and PPAR{alpha}-Null Mice Exposed to Perfluorooctanoic Acid Toxicol Pathol, June 1, 2008; 36(4): 592 - 607. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
C. Lau, K. Anitole, C. Hodes, D. Lai, A. Pfahles-Hutchens, and J. Seed Perfluoroalkyl Acids: A Review of Monitoring and Toxicological Findings Toxicol. Sci., October 1, 2007; 99(2): 366 - 394. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
H.-Q. Yin, M. Kim, J.-H. Kim, G. Kong, M.-O. Lee, K.-S. Kang, B.-I. Yoon, H.-L. Kim, and B.-H. Lee Hepatic Gene Expression Profiling and Lipid Homeostasis in Mice Exposed to Steatogenic Drug, Tetracycline Toxicol. Sci., November 1, 2006; 94(1): 206 - 216. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
J. P. Vanden Heuvel, J. T. Thompson, S. R. Frame, and P. J. Gillies Differential Activation of Nuclear Receptors by Perfluorinated Fatty Acid Analogs and Natural Fatty Acids: A Comparison of Human, Mouse, and Rat Peroxisome Proliferator-Activated Receptor-{alpha}, -{beta}, and -{gamma}, Liver X Receptor-{beta}, and Retinoid X Receptor-{alpha} Toxicol. Sci., August 1, 2006; 92(2): 476 - 489. [Abstract] [Full Text] [PDF]
|
|