CCAAT enhancer binding protein beta and hepatocyte nuclear factor 3beta are necessary and sufficient to mediate dexamethasone-induced up-regulation of alpha2HS-glycoprotein/fetuin-A gene expression

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Michael Wöltje - , Universitätsklinikum Aachen (Autor:in)
  • Beate Tschöke - (Autor:in)
  • Verena von Bülow - (Autor:in)
  • Ralf Westenfeld - (Autor:in)
  • Bernd Denecke - (Autor:in)
  • Steffen Gräber - (Autor:in)
  • Willi Jahnen-Dechent - (Autor:in)

Abstract

Alpha2HS-glycoprotein/fetuin-A (Ahsg) is a serum protein preventing soft tissue calcification. In trauma and inflammation, Ahsg is down-regulated and therefore considered a negative acute phase protein. Enhancement of Ahsg expression as a protective serum protein is desirable in several diseases including tissue remodelling after trauma and infection, kidney and heart failure, and cancer. Using reporter gene assays in hepatoma cells combined with electrophoretic mobility shift assays we determined that dexamethasone up-regulates hepatic Ahsg. A steroid response unit at position -146/-119 within the mouse Ahsg promoter mediates the glucocorticoid-induced increase of Ahsg mRNA. It binds the hepatocyte nuclear factor 3beta and CCAAT enhancer binding protein beta (C/EBP-beta). The up-regulation is mediated indirectly via glucocorticoid hormone-induced transcriptional up-regulation in C/EBP-beta protein. A high degree of sequence identity in mouse, rat and human Ahsg promoters suggests that the promoter is similarly up-regulated by dexamethasone in all three species. Therefore, our findings suggest that glucocorticoids may be used to enhance the level of Ahsg protein circulating in serum.

Details

OriginalspracheEnglisch
Seiten (von - bis)261-77
Seitenumfang17
FachzeitschriftJournal of molecular endocrinology
Jahrgang36
Ausgabenummer2
PublikationsstatusVeröffentlicht - Apr. 2006
Peer-Review-StatusJa
Extern publiziertJa

Externe IDs

Scopus 33646129683

Schlagworte

Ziele für nachhaltige Entwicklung

Schlagwörter

  • Animals, Base Sequence, Blood Proteins/genetics, CCAAT-Enhancer-Binding Protein-beta/genetics, Cells, Cultured, Cycloheximide/pharmacology, Dexamethasone/pharmacology, Glucocorticoids/pharmacology, Hepatocyte Nuclear Factor 3-beta/genetics, Humans, Mice, Molecular Sequence Data, Promoter Regions, Genetic/genetics, Protein Binding, RNA, Messenger/genetics, Receptors, Glucocorticoid/genetics, Sequence Alignment, Transcription, Genetic/genetics, Up-Regulation/drug effects, alpha-2-HS-Glycoprotein, alpha-Fetoproteins/genetics