Journal Article

Downregulation of Lactoferrin by PPARα Ligands: Role in Perturbation of Hepatocyte Proliferation and Apoptosis

Susan Hasmall, George Orphanides, Neil James, William Pennie, Kathryn Hedley, Anthony Soames, Ian Kimber and Ruth Roberts

in Toxicological Sciences

Volume 68, issue 2, pages 304-313
Published in print August 2002 | ISSN: 1096-6080
Published online August 2002 | e-ISSN: 1096-0929 | DOI: http://dx.doi.org/10.1093/toxsci/68.2.304
Downregulation of Lactoferrin by PPARα Ligands: Role in Perturbation of Hepatocyte Proliferation and Apoptosis

More Like This

Show all results sharing these subjects:

  • Medical Toxicology
  • Toxicology (Non-medical)

GO

Show Summary Details

Preview

PPARα (peroxisome proliferator activated receptor α) is a transcription factor that mediates the rodent liver tumorigenic responses to peroxisome proliferators via regulation of genes that remain to be identified. Using microarray gene expression profiling of mRNA from wild type versus PPARα null mice, we detected a 3- to 7-fold downregulation of hepatic lactoferrin (LF) in response to the PP, diethylhexylphthalate (DEHP; 1150 mg/kg). Northern blot analyses confirmed a significant downregulation of LF mRNA by DEHP in wild type mouse liver. Since LF has been reported to repress tumor necrosis factor-α (TNF-α), LF downregulation by PPs may permit TNF-α levels to rise, enhancing hepatocyte survival and proliferation. To test this hypothesis, we asked if exogenous LF could prevent the perturbation of hepatocyte growth by PPs but not by TNF-α. In vitro, the PPs monoethylhexylphthalate (MEHP; 500 μM, the active metabolite of DEHP) and another PP, nafenopin (50 μM) or exogenous TNF-α (5000 U/ml) induced hepatocyte proliferation and suppressed apoptosis. LF (200 μM) blocked the growth but not the peroxisome proliferation response to PPs but could not block the growth response to TNF-α. Immunocytochemistry using specific antibodies to LF but also to transferrin (TF), a related gene previously shown to contain a PP response element (PPRE), demonstrated that both LF and TF are expressed in murine liver. Furthermore, both were downregulated by DEHP in both wild type and PPARα null mouse liver. These data suggest that the regulation of iron binding proteins by PPARα ligands plays a role in PP-mediated liver growth, but not in peroxisome proliferation.

Keywords: nongenotoxic carcinogenesis; lactoferrin; peroxisome proliferators; PPARα; hypolipidaemic drugs

Journal Article.  6429 words.  Illustrated.

Subjects: Medical Toxicology ; Toxicology (Non-medical)

Full text: subscription required

How to subscribe Recommend to my Librarian

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.