From the Section on Molecular Medicine, Department of Internal Medicine (H.C., M.L., C.-C.C.K., E.B., J.K.S., A.W., A.B., J.S.P.) and Department of Biochemistry (J.S.P.), Wake Forest School of Medicine, Winston-Salem, NC; Diabetes, Obesity and Metabolism Institute, Icahn School of Medicine at Mount Sinai, New York (S.K.F.); and Department of Nutrition and Health Sciences, University of Nebraska, Lincoln, NE (S.C.).
Arterioscler Thromb Vasc Biol. 2018 Apr;38(4):733-743. doi: 10.1161/ATVBAHA.117.309880. Epub 2018 Jan 18.
Adipose tissue cholesterol increases with adipocyte triglyceride content and size during development of obesity. However, how adipocyte cholesterol affects adipocyte function is poorly understood. The aim of this study was to evaluate the role of the cellular cholesterol exporter, Abca1 (ATP-binding cassette transporter A1), on adipose tissue function during diet-induced obesity.
Adiponectin recombinase transgenic mice were crossed with mice to generate ASKO (adipocyte-specific knockout) mice. Control and ASKO mice were then fed a high-fat, high-cholesterol (45% calories as fat and 0.2% cholesterol) diet for 16 weeks. Compared with control mice, ASKO mice had a 2-fold increase in adipocyte plasma membrane cholesterol content and significantly lower body weight, epididymal fat pad weight, and adipocyte size. ASKO versus control adipose tissue had decreased PPARγ (peroxisome proliferator-activated receptor γ) and CCAAT/enhancer-binding protein expression, nuclear SREBP1 (sterol regulatory element-binding protein 1) protein, lipogenesis, and triglyceride accretion but similar Akt activation after acute insulin stimulation. Acute siRNA-mediated silencing during 3T3L1 adipocyte differentiation reduced adipocyte Abca1 and PPARγ protein expression and triglyceride content. Systemic stimulated triglyceride lipolysis and glucose homeostasis were similar between control and ASKO mice.
Adipocyte Abca1 is a key regulator of adipocyte lipogenesis and lipid accretion, likely because of increased adipose tissue membrane cholesterol, resulting in decreased activation of lipogenic transcription factors PPARγ and SREBP1.
在肥胖的发展过程中,脂肪组织中的胆固醇随着脂肪细胞甘油三酯含量和大小的增加而增加。然而,脂肪细胞胆固醇如何影响脂肪细胞功能还知之甚少。本研究旨在评估细胞胆固醇外排器 Abca1(ATP 结合盒转运体 A1)在饮食诱导肥胖期间对脂肪组织功能的作用。
将脂联素重组酶转基因小鼠与 小鼠杂交,生成 ASKO(脂肪细胞特异性 敲除)小鼠。然后,对照和 ASKO 小鼠分别喂食高脂肪、高胆固醇(45%热量来自脂肪和 0.2%胆固醇)饮食 16 周。与对照小鼠相比,ASKO 小鼠的脂肪细胞膜胆固醇含量增加了 2 倍,体重、附睾脂肪垫重量和脂肪细胞大小明显降低。与对照脂肪组织相比,ASKO 脂肪组织中的 PPARγ(过氧化物酶体增殖物激活受体 γ)和 CCAAT/增强子结合蛋白表达、核 SREBP1(固醇调节元件结合蛋白 1)蛋白、脂肪生成和甘油三酯积累减少,但急性胰岛素刺激后 Akt 激活相似。在 3T3L1 脂肪细胞分化过程中,急性 siRNA 介导的沉默降低了脂肪细胞 Abca1 和 PPARγ蛋白表达和甘油三酯含量。对照和 ASKO 小鼠之间的系统性刺激甘油三酯脂肪分解和葡萄糖稳态相似。
脂肪细胞 Abca1 是脂肪细胞脂肪生成和脂质积累的关键调节剂,可能是由于脂肪组织膜胆固醇增加,导致脂肪生成转录因子 PPARγ 和 SREBP1 的激活减少。