dc.contributor.author
García-Alonso, Verónica
dc.contributor.author
López Vicario, Cristina
dc.contributor.author
Titos Rodríguez, Esther
dc.contributor.author
Morán-Salvador, Eva
dc.contributor.author
González Périz, Ana
dc.contributor.author
Rius, Bibiana
dc.contributor.author
Párrizas, Marcelina
dc.contributor.author
Werz, Oliver
dc.contributor.author
Arroyo, Vicente
dc.contributor.author
Clària i Enrich, Joan
dc.date.issued
2017-03-20T07:59:14Z
dc.date.issued
2017-03-20T07:59:14Z
dc.date.issued
2013-08-13
dc.date.issued
2017-03-20T07:59:15Z
dc.identifier
https://hdl.handle.net/2445/108602
dc.description.abstract
Peroxisome 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
application/pdf
dc.publisher
American Society for Biochemistry and Molecular Biology
dc.relation
Reproducció del document publicat a: https://doi.org/10.1074/jbc.M113.468603
dc.relation
Journal of Biological Chemistry, 2013, vol. 288, num. 39, p. 28230-28242
dc.relation
https://doi.org/10.1074/jbc.M113.468603
dc.rights
(c) American Society for Biochemistry and Molecular Biology, 2013
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Biomedicina)
dc.subject
Prostaglandines
dc.subject
Trastorns del metabolisme
dc.subject
Regulació del metabolisme
dc.subject
Adipose tissues
dc.subject
Prostaglandins
dc.subject
Disorders of metabolism
dc.subject
Metabolic regulation
dc.title
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.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion