Millet L, Vidal H, Andreelli F, Larrouy D, Riou J P, Ricquier D, Laville M, Langin D
Institut National de la Santé et de la Recherche Médicale Unité 317, Institut Louis Bugnard, Université Paul Sabatier, Bâtiment L3, Hôpital Rangueil, 31403 Toulouse Cedex 4, France.
J Clin Invest. 1997 Dec 1;100(11):2665-70. doi: 10.1172/JCI119811.
Uncoupling protein-2 and -3 (UCP2 and UCP3) are mitochondrial proteins that show high sequence homology with the brown adipocyte-specific UCP1. UCP1 induces heat production by uncoupling respiration from ATP synthesis. UCP2 is widely expressed in human tissues, whereas UCP3 expression seems restricted to skeletal muscle, an important site of thermogenesis in humans. We have investigated the regulation of UCP2 and UCP3 gene expression in skeletal muscle and adipose tissue from lean and obese humans. UCP2 and -3 mRNA levels were not correlated with body mass index (BMI) in skeletal muscle, but a positive correlation (r = 0.55, P < 0.01, n = 22) was found between UCP2 mRNA level in adipose tissue and BMI. The effect of fasting was investigated in eight lean and six obese subjects maintained on a hypocaloric diet (1,045 kJ/d) for 5 d. Calorie restriction induced a similar 2-2.5-fold increase in UCP2 and -3 mRNA levels in lean and obese subjects. To study the effect of insulin on UCP gene expression, six lean and five obese subjects underwent a 3-h euglycemic hyperinsulinemic clamp. Insulin infusion did not modify UCP2 and -3 mRNA levels. In conclusion, the similar induction of gene expression observed during fasting in lean and obese subjects shows that there is no major alteration of UCP2 and -3 gene regulation in adipose tissue and skeletal muscle of obese subjects. The increase in UCP2 and -3 mRNA levels suggests a role for these proteins in the metabolic adaptation to fasting.
解偶联蛋白-2和-3(UCP2和UCP3)是线粒体蛋白,与棕色脂肪细胞特异性的UCP1具有高度的序列同源性。UCP1通过使呼吸与ATP合成解偶联来诱导产热。UCP2在人体组织中广泛表达,而UCP3的表达似乎局限于骨骼肌,这是人体产热的一个重要部位。我们研究了瘦人和肥胖者骨骼肌和脂肪组织中UCP2和UCP3基因表达的调控情况。骨骼肌中UCP2和-3的mRNA水平与体重指数(BMI)无关,但脂肪组织中UCP2的mRNA水平与BMI呈正相关(r = 0.55,P < 0.01,n = 22)。对8名瘦人和6名肥胖者进行了研究,他们维持低热量饮食(1045千焦/天)5天,以研究禁食的影响。热量限制使瘦人和肥胖者的UCP2和-3的mRNA水平都有类似的2 - 2.5倍的升高。为了研究胰岛素对UCP基因表达的影响,6名瘦人和5名肥胖者接受了3小时的正常血糖高胰岛素钳夹试验。胰岛素输注并未改变UCP2和-3的mRNA水平。总之,在瘦人和肥胖者禁食期间观察到的基因表达的类似诱导表明,肥胖者脂肪组织和骨骼肌中UCP2和-3基因调控没有重大改变。UCP2和-3的mRNA水平升高表明这些蛋白质在对禁食的代谢适应中发挥作用。