Stimulation of selenoprotein P promoter activity in hepatoma cells by FoxO1a transcription factor.

Abstract

Selenoprotein P (SeP) is the major selenoprotein in human plasma, acting as an antioxidant and serving the transport of selenium from the liver to extrahepatic tissues. We here demonstrate that the human SeP promoter responds to overexpression of FoxO1a as well as of a constitutively active form of FoxO1a. Two FoxO-responsive elements were identified and characterized by generation of point mutation and deletion constructs. Similarly, SeP mRNA was upregulated in response to activation of FoxO1a in rat hepatoma cells stably transfected with a hydroxytamoxifen-regulatable form of FoxO1a. Insulin, stimulating the phosphorylation and inactivation of FoxO1a via phosphoinositide 3-kinase (PI3K) and Akt, suppressed SeP promoter activity and mRNA synthesis. This suppressive effect of insulin on SeP expression was attenuated by inhibitors of PI3K. In conclusion, the selenoprotein P promoter is a target of the Akt/FoxO signal transduction cascade and SeP expression is regulated at the level of transcription by the forkhead box protein FoxO1a in human and rat hepatoma cells.

• Authors: Philippe L Walter, Holger Steinbrenner, Andreas Barthel, Lars-Oliver Klotz
• Journal: Biochemical and biophysical research communications (Biochem Biophys Res Commun) Vol. 365 Issue 2 Pg. 316-21 (Jan 11 2008) ISSN: 1090-2104 [Electronic] United States
• PMID: 17986386 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• FOXO1 protein, human
• Forkhead Box Protein O1
• Forkhead Transcription Factors
• Selenoprotein P
• Transcription Factors

Topics

• Animals
• Carcinoma, Hepatocellular (genetics, metabolism)
• Cell Line
• Cells, Cultured
• Forkhead Box Protein O1
• Forkhead Transcription Factors (metabolism)
• Humans
• Promoter Regions, Genetic (genetics)
• Rats
• Selenoprotein P (metabolism)
• Transcription Factors (genetics, metabolism)