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PMID: 8524934 Published · ppublish English Journal Article

Mechanisms of transcriptional activation of lipopolysaccharide binding protein (LBP).

Progress in clinical and biological research ·Vol. 392 ·1995-00-00 ·Pages 297-304

Schumann RR

Abstract

The Lipopolysaccharide Binding Protein (LBP) is of high importance for endotoxin recognition, presentation and subsequent cytokine induction in immune cells. LBP, which is a member of a growing family of structurally and functionally related proteins, is synthesized in hepatocytes and secreted into the blood stream constitutively. During the acute phase response, however, LBP levels rise substantially and here the mechanisms of induction of LBP protein synthesis were reviewed. The induction of LBP in hepatocytes is due to transcriptional and posttranscriptional mechanisms as we have shown by nuclear run-on and RNA half-life experiments. Cloning of the 5'-flanking region of the LBP gene, furthermore revealed a typical acute phase protein promoter. Reporter gene assays employing the luciferase gene and mutation variants of the LBP promoter revealed that integrity of a common acute phase promoter motif, named APRE/STAT-3 is essential for activation of the LBP promoter. Elucidation of the transcriptional activation mechanism could point the way to a therapeutically lowering of LBP levels in high risk patients for reducing their susceptibility to Gram-negative septic shock.

MeSH Terms
Acute-Phase Proteins/biosynthesis,genetics,metabolism Animals Carrier Proteins/biosynthesis,genetics,metabolism Gram-Negative Bacterial Infections/prevention & control Humans Lipopolysaccharides/metabolism,toxicity Liver/metabolism Membrane Glycoproteins Promoter Regions, Genetic RNA, Messenger/genetics,metabolism Shock, Septic/prevention & control Toxemia/prevention & control Transcriptional Activation
Chemicals
Acute-Phase Proteins Carrier Proteins Lipopolysaccharides Membrane Glycoproteins RNA, Messenger lipopolysaccharide-binding protein
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Schumann R R
Max-Delbrück-Centrum für Molekulare Medizin (MDC), Robert-Rössle-Cancer Center, University Hospital Rudolf-Virchow, Free University of Berlin, Germany.
Article Info
Journal
Progress in clinical and biological research
Abbr.
Prog Clin Biol Res
ISSN
0361-7742
Published
1995-00-00
Pages
297-304
Language
English
Region
United States
NLM ID
7605701
Subset
IM
External Links
PubMed source
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