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.

Highlights

  • Microsomal prostaglandin E (PGE) synthase-1 is an inducible enzyme with unknown properties in adipose homeostasis

  • We present evidence that mice lacking PPAR␥ in the adipose tissue are resistant to high fat diet (HFD)-induced Epididymal WAT (eWAT) formation by mechanisms linked to prostaglandin E2 (PGE2) biosynthesis

  • Our study demonstrates the induction of Microsomal prostaglandin E (PGE) synthase-1 (mPGES-1) expression and augmented PGE2 levels in eWAT from aP2-Cre peroxisome proliferator-activated receptor ␥ (PPAR␥)deficient mice

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Summary

Background

Microsomal prostaglandin E (PGE) synthase-1 (mPGES-1) is an inducible enzyme with unknown properties in adipose homeostasis. In this study we demonstrate the existence of a coordinate functional interaction between PPAR␥ and mPGES-1 in controlling the process of preadipocyte differentiation in white adipose tissue (WAT). The effects of PGE2 on pre-adipocyte differentiation were not seen in mice lacking PPAR␥ 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 PPAR␥ and mPGES-1. PGE2 is recognized as a negative regulator of WAT lipolysis and adipocyte development [14, 15], and preadipocytes stably transfected with either COX-1 or COX-2 show lower PPAR␥ expression [16] Consistent with this view, mice genetically deficient for mPGES-1 show basal elevations in PPAR␥ expression and transcriptional activity [17]. Our results demonstrate that removing PPAR␥ in fat cells triggers mPGES-1 expression and PGE2 biosynthesis, uncovering an important role in the browning process of WAT pre-adipocytes

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