Rao Poornima, Huang Zhi Hua, Mazzone Theodore
Department of Medicine, University of Illinois at Chicago, Chicago, Illinois 60612, USA.
J Clin Endocrinol Metab. 2007 Nov;92(11):4366-72. doi: 10.1210/jc.2007-1592. Epub 2007 Sep 4.
Obesity is increasing in prevalence and it is important to understand factors that regulate adipose tissue lipid metabolism. Recently, endogenous expression of apolipoprotein E (apoE) in adipose tissue has been shown to have important effects on adipocyte lipid flux and gene expression. Adipose tissue is also a physiological target of angiotensin II (AII).
The aim of the current study was to evaluate a potential regulatory effect for AII on adipose tissue apoE expression.
Infusion of AII into mice for 3 d significantly reduced apoE expression in adipocytes from freshly isolated adipose tissue. ApoE expression was unchanged by the AII infusion in the stromovascular fraction. In isolated human adipocytes, treatment with AII significantly reduced cellular and secreted apoprotein E (by 20-60%). Suppression of apoE expression was observed in sc adipocytes obtained from nonobese (body mass index < 30 kg/m(2)) donors, and in sc and omental adipocytes obtained from obese (body mass index > 30 kg/m(2)) donors. Evaluation of the effect of AII in matched sets of sc and omental adipocytes from three separate donors showed lower overall apoE expression in omental adipocytes in two of the donors, and a concordant down-regulation of apoE expression in sc and omental adipocytes from all three subjects. The specific AT(1) receptor blocker, valsartan, eliminated the effect of AII on adipocyte apoE expression.
Both apoE and components of the renin-angiotensin system are expressed in adipose tissue, and each has important effects on adipocyte lipid metabolism and gene expression. The regulatory interaction we have identified between these two pathways has important implications for a complete understanding of adipose tissue lipid homeostasis.
肥胖的患病率正在上升,了解调节脂肪组织脂质代谢的因素很重要。最近,已证明脂肪组织中载脂蛋白E(apoE)的内源性表达对脂肪细胞脂质通量和基因表达具有重要影响。脂肪组织也是血管紧张素II(AII)的生理靶点。
本研究的目的是评估AII对脂肪组织apoE表达的潜在调节作用。
给小鼠输注AII 3天可显著降低新鲜分离的脂肪组织中脂肪细胞的apoE表达。在血管基质部分,AII输注对apoE表达没有影响。在分离的人脂肪细胞中,用AII处理可显著降低细胞内和分泌的载脂蛋白E(降低20%-60%)。在从非肥胖(体重指数<30 kg/m²)供体获得的皮下脂肪细胞以及从肥胖(体重指数>30 kg/m²)供体获得的皮下和网膜脂肪细胞中均观察到apoE表达受到抑制。对来自三个不同供体的匹配皮下和网膜脂肪细胞组中AII的作用进行评估,结果显示在其中两个供体的网膜脂肪细胞中总体apoE表达较低,并且在所有三个受试者的皮下和网膜脂肪细胞中apoE表达均一致下调。特异性AT1受体阻滞剂缬沙坦消除了AII对脂肪细胞apoE表达的影响。
apoE和肾素-血管紧张素系统的成分均在脂肪组织中表达,并且各自对脂肪细胞脂质代谢和基因表达具有重要影响。我们所确定的这两条途径之间的调节相互作用对于全面理解脂肪组织脂质稳态具有重要意义。