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A mutation in the peroxisome proliferator-activated receptor γ-binding site in the gene for the cytosolic form of phosphoenolpyruvate carboxykinase reduces adipose tissue size and fat content in mice

机译:磷酸烯醇丙酮酸羧化激酶胞质形式的基因中过氧化物酶体增殖物激活的受体γ结合位点的突变减少了小鼠的脂肪组织大小和脂肪含量

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摘要

Regulation of the turnover of triglycerides in adipose tissue requires the continuous provision of 3-glycerophosphate, which may be supplied by the metabolism of glucose or by glyceroneogenesis, the de novo synthesis of 3-glycerophosphate from sources other than hexoses or glycerol. The importance of glyceroneogenesis in adipose tissue was assessed in mice by specifically eliminating the expression of the cytosolic form of phosphoenolpyruvate carboxykinase (PEPCK-C), an enzyme that plays a pivotal role in the pathway. To accomplish this, we mutated the binding site for the peroxisome proliferator-activated receptor γ (PPARγ) called the peroxisome proliferator-activated receptor element (PPARE), in the 5′ flanking region of the PEPCK-C gene in the mouse by homologous recombination. The mutation abolished expression of the gene in white adipose tissue and considerably reduced its expression in brown adipose tissue, whereas the level of PEPCK-C mRNA in liver and kidney remained normal. Epididymal white adipose tissue from these mice had a reduced triglyceride deposition, with 25% of the animals displaying lipodystrophy. There was also a greatly reduced level of lipid accumulation in brown adipose tissue. A strong correlation between the hepatic content of triglycerides and the size of the epididymal fat pad in PPARE−/− mice suggests that hepatic triglyceride synthesis predominantly utilizes free fatty acids derived from the adipose tissue. Unlike other models, PPARE−/− mice with lipodystrophy did not exhibit the lipodystrophy-associated features of diabetes and displayed only moderate hyperglycemia. These studies establish the importance of the PPARE site for PEPCK-C gene expression in adipose tissue and the role of PEPCK-C in the regulation of glyceroneogenesis, a pathway critical for maintaining the deposition of triglycerides in adipose tissue.
机译:调节脂肪组织中甘油三酸酯的周转需要连续提供3-甘油磷酸酯,这可以通过葡萄糖的代谢或甘油生成,从己糖或甘油以外的来源从头合成3-甘油磷酸酯来提供。通过特异性消除磷酸烯醇丙酮酸羧化激酶(PEPCK-C)(一种在该途径中起关键作用的酶)的胞浆形式的表达,评估了小鼠脂肪组织中甘油生成的重要性。为此,我们通过同源重组在小鼠PEPCK-C基因的5'侧翼区域突变了过氧化物酶体增殖物激活受体γ(PPARγ)的结合位点,称为过氧化物酶体增殖物激活受体元件(PPARE)。 。该突变消除了该基因在白色脂肪组织中的表达,并大大降低了其在棕色脂肪组织中的表达,而肝脏和肾脏中PEPCK-C mRNA的水平保持正常。这些小鼠的附睾白色脂肪组织的甘油三酸酯沉积减少,其中25%的动物表现出脂肪营养不良。棕色脂肪组织中的脂质蓄积水平也大大降低。在PPARE-/-小鼠中,甘油三酸酯的肝含量与附睾脂肪垫的大小之间存在很强的相关性,这表明肝脏合成甘油三酸酯主要利用源自脂肪组织的游离脂肪酸。与其他模型不同,患有脂肪营养不良的PPARE-/-小鼠没有表现出与脂肪营养不良相关的糖尿病特征,仅表现出中度高血糖。这些研究确立了PPARE位点对于脂肪组织中PEPCK-C基因表达的重要性,以及PEPCK-C在调节甘油生成中的作用,而甘油生成是维持甘油三酸酯在脂肪组织中沉积的关键途径。

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