Manioc : Portail | resultats 1 - 20 pour la recherche: Pommier, Aurélien

L'Église et l'esclavage
Auteur(s) : Rivière, Armand (1822-1891)
Année de publication :

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Annuaire de la vie martiniquaise : 1936
Auteur(s) : Sylvestre, Emile (1...-19.. ; fonctionnaire) Lotaut, Eustache
Auteurs secondaires : Eboué, Félix (1884-1944)
Année de publication :

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Géographie complète et universelle : illustrée de 50 gravures, 8 cartes, 5 planches et du portrait de l'auteur. Tome deuxième
Auteur(s) : Malte-Brun, Conrad (1775-1826)
Auteurs secondaires : Malte-Brun, Victor-Adolphe (1816-1889)
Année de publication :

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Géographie complète et universelle : illustrée de 50 gravures, 8 cartes, 5 planches et du portrait de l'auteur. Tome quatrième
Auteur(s) : Malte-Brun, Conrad (1775-1826)
Auteurs secondaires : Malte-Brun, Victor-Adolphe (1816-1889)
Année de publication :

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Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
The Liver X Receptors (LXRs) α and β and the Peroxisome Proliferator-Activated Receptor α (PPARα) are transcription factors that belong to class II nuclear receptors. They drive the expression of genes involved in hepatic lipid homeostasis and therefore are important targets for the prevention and treatment of nonalcoholic fatty liver disease (NAFLD). LXRs and PPARα are regulated by endogenous ligands, oxysterols and fatty acid derived molecules, respectively. In the liver, pharmacological activation of LXRs leads to the over-expression of genes involved in de novo lipogenesis, while PPARα is critical for fatty acid catabolism in nutrient deprivation. Even if these two nuclear receptors seemed to play opposite parts, recent studies have highlighted that PPARα also influence the expression of genes involved in fatty acids synthesis. In this study, we used pharmacological approaches and genetically engineered mice to investigate the cross-talk between LXRs and PPARα in the regulation of genes responsible for lipogenesis. We first investigated the effect of T0901317 and fenofibrate, two synthetic agonists of LXRs and PPARα, respectively. As expected, T0901317 and fenofibrate induce expression of genes involved LXR-dependent and PPARα-dependent lipogenic responses. Considering such overlapping effect, we then tested whether LXR agonist may influence PPARα driven response and vice versa. We show that the lack of PPARα does not influence the effects of T0901317 on lipogenic genes expression. However, PPARα deficiency prevents the up-regulation of genes involved in ω-hydroxylation that are induced by the LXR agonist. In addition, over-expression of lipogenic genes in response to fenofibrate is decreased in LXR knockout mice as well as the expression of PPARα target genes involved in fatty acid oxidation. Altogether, our work provides in vivo evidence for a central interconnection between nuclear receptors that drive hepatic lipid metabolism in response to oxysterol and fatty acids.
ISSN: 0300-9084

inserm-00872582
http://www.hal.inserm.fr/inserm-00872582
DOI : 10.1016/j.biochi.2012.09.028
PUBMED : 23063693

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