Rieusset J, Andreelli F, Auboeuf D, Roques M, Vallier P, Riou J P, Auwerx J, Laville M, Vidal H
INSERM U449 and the Human Nutrition Research Center of Lyon, France.
Diabetes. 1999 Apr;48(4):699-705. doi: 10.2337/diabetes.48.4.699.
Peroxisome proliferator-activated receptor (PPAR)-gamma is one of the key actors of adipocyte differentiation. This study demonstrates 1) that PPAR-gamma mRNA expression is not altered in subcutaneous adipose tissue (n = 44) or in skeletal muscle (n = 19) of subjects spanning a wide range of BMIs (20-53 kg/m2) and 2) that insulin acutely increases PPAR-gamma mRNA expression in human adipocytes both in vivo and in vitro. The effect of insulin was investigated in abdominal subcutaneous biopsies obtained before and at the end of a 3-h euglycemic-hyperinsulinemic clamp. Insulin significantly increased PPAR-gamma mRNA levels in lean subjects (88 +/- 17%, n = 6), in type 2 diabetic patients (100 +/- 19%, n = 6), and in nondiabetic obese patients (91 +/- 20%, n = 6). Both PPAR-gamma1 and PPAR-gamma2 mRNA variants were increased (P < 0.05) after insulin infusion. In isolated human adipocytes, insulin induced the two PPAR-gamma mRNAs in a dose-dependent manner, with half-maximal stimulation at a concentration of approximately 1-5 nmol/l. However, PPAR-gamma2 mRNA was rapidly (2 h) and transiently increased, whereas a slow and more progressive induction of PPAR-gamma1 was observed during the 6 h of incubation. In explants of human adipose tissue, PPAR-gamma protein levels were significantly increased (42 +/- 3%, P < 0.05) after 12 h of incubation with insulin. These data demonstrate that PPAR-gamma belongs to the list of the insulin-regulated genes and that obesity and type 2 diabetes are not associated with alteration in the expression of this nuclear receptor in adipose tissue.
过氧化物酶体增殖物激活受体(PPAR)-γ是脂肪细胞分化的关键因子之一。本研究表明:1)在广泛的体重指数(BMI,20 - 53kg/m²)范围内,受试者的皮下脂肪组织(n = 44)或骨骼肌(n = 19)中PPAR-γ mRNA表达未发生改变;2)胰岛素可在体内和体外急性增加人脂肪细胞中PPAR-γ mRNA的表达。在3小时正常血糖-高胰岛素钳夹试验前后获取的腹部皮下活检组织中研究了胰岛素的作用。胰岛素显著增加了瘦人(88±17%,n = 6)、2型糖尿病患者(100±19%,n = 6)和非糖尿病肥胖患者(91±20%,n = 6)的PPAR-γ mRNA水平。胰岛素输注后,PPAR-γ1和PPAR-γ2 mRNA变体均增加(P < 0.05)。在分离的人脂肪细胞中,胰岛素以剂量依赖方式诱导两种PPAR-γ mRNA表达,浓度约为1 - 5nmol/l时达到半数最大刺激。然而,PPAR-γ2 mRNA迅速(2小时)且短暂增加,而在孵育6小时期间观察到PPAR-γ1的诱导较为缓慢且呈渐进性。在人脂肪组织外植体中,与胰岛素孵育12小时后,PPAR-γ蛋白水平显著增加(42±3%,P < 0.05)。这些数据表明PPAR-γ属于胰岛素调节基因列表,且肥胖和2型糖尿病与该核受体在脂肪组织中的表达改变无关。