Vasoactive intestinal peptide, pituitary adenylate cyclase-activating peptide, and noradrenaline induce the transcription factors CCAAT/enhancer binding protein (C/EBP)-beta and C/EBP delta in mouse cortical astrocytes: involvement in cAMP-regulated glycogen metabolism.

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Version: Final published version
ID Serval
serval:BIB_2A9ED0B306D3
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Vasoactive intestinal peptide, pituitary adenylate cyclase-activating peptide, and noradrenaline induce the transcription factors CCAAT/enhancer binding protein (C/EBP)-beta and C/EBP delta in mouse cortical astrocytes: involvement in cAMP-regulated glycogen metabolism.
Périodique
Journal of Neuroscience
Auteur(s)
Cardinaux J.R., Magistretti P.J.
ISSN
0270-6474
Statut éditorial
Publié
Date de publication
1996
Peer-reviewed
Oui
Volume
16
Numéro
3
Pages
919-929
Langue
anglais
Résumé
We have described previously a transcription-dependent induction of glycogen resynthesis by the vasoactive intestinal peptide (VIP) or noradrenaline (NA) in astrocytes, which is mediated by cAMP. Because it has been postulated that the cAMP-mediated regulation of energy balance in hepatocytes and adipocytes is channeled at least in part through the CCAAT/enhancer binding protein (C/EBP) family of transcription factors, we tested the hypothesis that C/EBP isoforms could be expressed in mouse cortical astrocytes and that their level of expression could be regulated by VIP, by the VIP-related neuropeptide pituitary adenylate cyclase-activating peptide (PACAP), or by NA. We report in this study that in these cells, C/EBP beta and C/EBP delta are induced by VIP, PACAP, or NA via the cAMP second-messenger pathway. Induction of C/EBP beta and -delta mRNA by VIP occurs in the presence of a protein synthesis inhibitor. Thus, c/ebp beta and c/ebp delta behave as cAMP-inducible immediate-early genes in astrocytes. Moreover, transfection of astrocytes with expression vectors selectively producing the transcriptionally active form of C/EBP beta, termed liver-enriched transcriptional activator protein, or C/EBP delta enhance the glycogen resynthesis elicited by NA, whereas an expression vector producing the transcriptionally inactive form of C/EBP beta, termed liver-enriched transcriptional inhibitory protein, reduces this resynthesis. These results support the idea that C/EBP beta and -delta regulate gene expression of energy metabolism-related enzymes in astrocytes.
Mots-clé
8-Bromo Cyclic Adenosine Monophosphate, Animals, Anisomycin, Astrocytes, CCAAT-Enhancer-Binding Protein-delta, CCAAT-Enhancer-Binding Proteins, Cells, Cultured, Cerebral Cortex, Cyclic AMP, DNA-Binding Proteins, Energy Metabolism, Forskolin, Gene Expression Regulation, Genes, Immediate-Early, Glycogen, Leucine Zippers, Mice, Nerve Tissue Proteins, Neuropeptides, Norepinephrine, Nuclear Proteins, Pituitary Adenylate Cyclase-Activating Polypeptide, Protein Synthesis Inhibitors, Second Messenger Systems, Transcription Factors, Transcription, Genetic, Vasoactive Intestinal Peptide
Pubmed
Web of science
Création de la notice
18/02/2008 10:32
Dernière modification de la notice
20/08/2019 13:10
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