Characterization of the fasting-induced adipose factor FIAF, a novel peroxisome proliferator-activated receptor target gene.
Détails
ID Serval
serval:BIB_4B2A552A1FDC
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Characterization of the fasting-induced adipose factor FIAF, a novel peroxisome proliferator-activated receptor target gene.
Périodique
Journal of Biological Chemistry
ISSN
0021-9258[print], 0021-9258[linking]
Statut éditorial
Publié
Date de publication
2000
Volume
275
Numéro
37
Pages
28488-28493
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Publication Status: ppublish
Résumé
Fasting is associated with significant changes in nutrient metabolism, many of which are governed by transcription factors that regulate the expression of rate-limiting enzymes. One factor that plays an important role in the metabolic response to fasting is the peroxisome proliferator-activated receptor alpha (PPARalpha). To gain more insight into the role of PPARalpha during fasting, and into the regulation of metabolism during fasting in general, a search for unknown PPARalpha target genes was performed. Using subtractive hybridization (SABRE) comparing liver mRNA from wild-type and PPARalpha null mice, we isolated a novel PPARalpha target gene, encoding the secreted protein FIAF (for fasting induced adipose factor), that belongs to the family of fibrinogen/angiopoietin-like proteins. FIAF is predominantly expressed in adipose tissue and is strongly up-regulated by fasting in white adipose tissue and liver. Moreover, FIAF mRNA is decreased in white adipose tissue of PPARgamma +/- mice. FIAF protein can be detected in various tissues and in blood plasma, suggesting that FIAF has an endocrine function. Its plasma abundance is increased by fasting and decreased by chronic high fat feeding. The data suggest that FIAF represents a novel endocrine signal involved in the regulation of metabolism, especially under fasting conditions.
Mots-clé
Adipose Tissue/metabolism, Amino Acid Sequence, Angiopoietins, Animals, Base Sequence, Blood Proteins/analysis, Blood Proteins/genetics, Fasting, Mice, Molecular Sequence Data, RNA, Messenger/analysis, Receptors, Cytoplasmic and Nuclear/physiology, Transcription Factors/physiology
Pubmed
Web of science
Open Access
Oui
Création de la notice
24/01/2008 15:27
Dernière modification de la notice
20/08/2019 13:59