From the Department of Biochemistry and Molecular Genetics, Hospital Clínic-IDIBAPS-Esther Koplowitz Center, Barcelona 08036, Spain.
J Biol Chem. 2013 Sep 27;288(39):28230-42. doi: 10.1074/jbc.M113.468603. Epub 2013 Aug 13.
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.
过氧化物酶体增殖物激活受体 γ(PPARγ)是一种配体激活的核受体,也是脂肪生成的主调控因子。微粒体前列腺素 E(PGE)合酶-1(mPGES-1)是一种诱导型酶,与环氧化酶-2 结合用于合成 PGE2。在这项研究中,我们证明了 PPARγ 和 mPGES-1 之间存在协调的功能相互作用,以控制白色脂肪组织(WAT)中前脂肪细胞分化的过程。携带 aP2 启动子驱动的 Cre 重组酶转基因的脂肪细胞特异性 PPARγ 敲除小鼠对高脂肪饮食的脂肪生成作用反应迟钝。这些敲除小鼠的前脂肪细胞失去了 PPARγ,并且对罗格列酮诱导的 WAT 分化具有抗性。与此同时,这些小鼠的 WAT 中解偶联蛋白 1 的表达增加,解偶联蛋白 1 是一种线粒体酶,可将化学能转化为热能。缺乏 PPARγ 的脂肪组织也表现出 mPGES-1 的上调和 PGE2 水平的增加。反过来,PGE2 抑制 PPARγ 表达并阻断罗格列酮诱导的前脂肪细胞向白色脂肪细胞分化,同时直接升高解偶联蛋白 1 表达并将前脂肪细胞分化为成熟的米色/棕色脂肪细胞。一致地,药理学抑制 mPGES-1 可使前脂肪细胞向白色脂肪细胞分化,同时抑制向米色/棕色脂肪细胞分化。使用针对 mPGES-1 的 siRNA 的敲低实验重现了这种褐色效应。在脂肪组织中缺乏 PPARγ 的小鼠中未观察到 PGE2 对前脂肪细胞分化的影响,也没有其他类二十烷酸(例如白三烯 B4)产生这种作用。综上所述,这些发现确定 PGE2 是白色至棕色脂肪生成的关键调节剂,并表明 PPARγ 和 mPGES-1 之间存在脂肪生成的协调调节。