Journal
JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 276, Issue 45, Pages 42485-42491Publisher
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M106480200
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- NCI NIH HHS [CA84472] Funding Source: Medline
- NIGMS NIH HHS [GM23750] Funding Source: Medline
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Peroxisome proliferators, which function as peroxisome proliferator-activated receptor alpha (PPAR alpha) agonists, induce peroxisomal, microsomal, and mitochondrial fatty acid oxidation enzymes, in conjunction with peroxisome proliferation, in liver cells. Sustained activation of PPAR alpha leads to the development of liver tumors in rats and mice. The assertion that synthetic PPAR alpha ligands pose negligible carcinogenic risk to humans is attributable, in part, to the failure to observe peroxisome proliferation in human hepatocytes. To explore the mechanism(s) of species-specific differences in response to PPAR alpha ligands, we determined the functional competency of human PPAR alpha in vivo and compared its potency with that of mouse PPAR alpha. Recombinant adenovirus that expresses human or mouse PPAR alpha was produced and administered intravenously to PPAR alpha -deficient mice. Human as well as mouse PPAR alpha fully restored the development of peroxisome proliferator-induced immediate pleiotropic responses, including peroxisome proliferation and enhanced expression of genes involved in lipid metabolism as well as nonperoxisomal genes, such as CD36, Ly-6D, Rbp7, monoglyceride lipase, pyruvate dehydrogenase kinase-4, and CV, that have been identified recently to be up-regulated in livers with peroxisome proliferation. These studies establish that human PPAR alpha is functionally competent and is equally as dose-sensitive as mouse PPAR alpha in inducing peroxisome proliferation within the context of mouse liver environment and that it can heterodimerize with mouse retinoid X receptor, and this human PPAR alpha -mouse retinoid X receptor chimeric heterodimer transcriptionally activates mouse PPAR alpha target genes in a manner qualitatively similar to that of mouse PPAR alpha.
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