Coordinate Functional Regulation between Microsomal Prostaglandin E Synthase-1 (mPGES-1) and Peroxisome Proliferator-activated Receptor y (PPARy) in the Conversion of White-to-brown Adipocytes

dc.contributor.authorGarcía-Alonso, Verónica
dc.contributor.authorLópez Vicario, Cristina
dc.contributor.authorTitos Rodríguez, Esther
dc.contributor.authorMorán-Salvador, Eva
dc.contributor.authorGonzález Périz, Ana
dc.contributor.authorRius, Bibiana
dc.contributor.authorPárrizas, Marcelina
dc.contributor.authorWerz, Oliver
dc.contributor.authorArroyo, Vicente
dc.contributor.authorClària i Enrich, Joan
dc.date.accessioned2017-03-20T07:59:14Z
dc.date.available2017-03-20T07:59:14Z
dc.date.issued2013-08-13
dc.date.updated2017-03-20T07:59:15Z
dc.description.abstractPeroxisome proliferator-activated receptor γ (PPARγ) is a ligand-activated nuclear receptor and a master regulator of adipogenesis. Microsomal prostaglandin E (PGE) synthase-1 (mPGES-1) is an inducible enzyme that couples with cyclooxygenase-2 for the biosynthesis of PGE2. In this study we demonstrate the existence of a coordinate functional interaction between PPARγ and mPGES-1 in controlling the process of pre-adipocyte differentiation in white adipose tissue (WAT). Adipocyte-specific PPARγ knock-out mice carrying an aP2 promoter-driven Cre recombinase transgene showed a blunted response to the adipogenic effects of a high fat diet. Pre-adipocytes from these knock-out mice showed loss of PPARγ and were resistant to rosiglitazone-induced WAT differentiation. In parallel, WAT from these mice showed increased expression of uncoupling protein 1, a mitochondrial enzyme that dissipates chemical energy as heat. Adipose tissue from mice lacking PPARγ also showed mPGES-1 up-regulation and increased PGE2 levels. In turn, PGE2 suppressed PPARγ expression and blocked rosiglitazone-induced pre-adipocyte differentiation toward white adipocytes while directly elevating uncoupling protein 1 expression and pre-adipocyte differentiation into mature beige/brite adipocytes. Consistently, pharmacological mPGES-1 inhibition directed pre-adipocyte differentiation toward white adipocytes while suppressing differentiation into beige/brite adipocytes. This browning effect was reproduced in knockdown experiments using a siRNA directed against mPGES-1. The effects of PGE2 on pre-adipocyte differentiation were not seen in mice lacking PPARγ in adipose tissue and were not mirrored by other eicosanoids (i.e. leukotriene B4). Taken together, these findings identify PGE2 as a key regulator of white-to-brown adipogenesis and suggest the existence of a coordinate regulation of adipogenesis between PPARγ and mPGES-1.
dc.format.extent17 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec627755
dc.identifier.issn0021-9258
dc.identifier.pmid23943621
dc.identifier.urihttps://hdl.handle.net/2445/108602
dc.language.isoeng
dc.publisherAmerican Society for Biochemistry and Molecular Biology
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1074/jbc.M113.468603
dc.relation.ispartofJournal of Biological Chemistry, 2013, vol. 288, num. 39, p. 28230-28242
dc.relation.urihttps://doi.org/10.1074/jbc.M113.468603
dc.rights(c) American Society for Biochemistry and Molecular Biology, 2013
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (Biomedicina)
dc.subject.classificationTeixit adipós
dc.subject.classificationProstaglandines
dc.subject.classificationTrastorns del metabolisme
dc.subject.classificationRegulació del metabolisme
dc.subject.otherAdipose tissues
dc.subject.otherProstaglandins
dc.subject.otherDisorders of metabolism
dc.subject.otherMetabolic regulation
dc.titleCoordinate Functional Regulation between Microsomal Prostaglandin E Synthase-1 (mPGES-1) and Peroxisome Proliferator-activated Receptor y (PPARy) in the Conversion of White-to-brown Adipocytes
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

Fitxers

Paquet original

Mostrant 1 - 1 de 1
Carregant...
Miniatura
Nom:
627755.pdf
Mida:
2.5 MB
Format:
Adobe Portable Document Format