Yoshida T, Hayashi M, Monkawa T, Saruta T
Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
Eur J Endocrinol. 1996 Nov;135(5):619-25. doi: 10.1530/eje.0.1350619.
The obese (ob) gene has been cloned recently and its protein product is called "leptin". Leptin is an adipocyte-derived satiety factor that regulates body weight homeostasis. Several hormonal factors have been reported to regulate ob mRNA expression. To determine which factors are most important for regulation of ob mRNA expression, we examined the effects of insulin, dexamethasone, a beta3-adrenergic agonist (CGP12177A), 8-bromo-cAMP, 8-bromo-cGMP and 1-methyl-3-isobutylxanthine (MIX) on primary cultured adipocytes. Rat adipocytes obtained from epididymal fat were cultured using the ceiling method. Total RNA was extracted and the expression of ob mRNA was measured by quantitative reverse transcription-polymerase chain reaction. After 24 h of incubation, 100 nmol/l insulin significantly increased the expression of ob mRNA (21.4-fold compared to control). Moreover, insulin increased ob mRNA expression in a dose-dependent manner over a range of 1-100 nmol/l. The effect of 100 nmol/l insulin was similar to that seen with 20% newborn calf serum. Dexamethasone (25-1000 nmol/l) also increased ob mRNA expression (2.5-2.9-fold). The effect of dexamethasone occurred more rapidly than insulin. CGP12177A (1-10 micromol/l) and 0.5 mmol/l 8-bromo-cAMP had no effects, whereas 0.5 mmol/l 8-bromo-cGMP and 0.5 mmol/l MIX had stimulatory effects (2.8- and 2.4-fold increase in ob mRNA, respectively). The combination of 250 nmol/l dexamethasone and 0.5 mmol/l MIX did not have an additive effect on ob mRNA levels. Our present data suggest that, of these agents, insulin is the most important factor regulating ob mRNA expression.
肥胖(ob)基因最近已被克隆,其蛋白质产物被称为“瘦素”。瘦素是一种由脂肪细胞产生的饱腹感因子,可调节体重平衡。据报道,有几种激素因子可调节ob mRNA的表达。为了确定哪些因子对ob mRNA表达的调节最为重要,我们研究了胰岛素、地塞米松、β3-肾上腺素能激动剂(CGP12177A)、8-溴-cAMP、8-溴-cGMP和1-甲基-3-异丁基黄嘌呤(MIX)对原代培养脂肪细胞的影响。采用悬滴法培养从附睾脂肪中获取的大鼠脂肪细胞。提取总RNA,并通过定量逆转录-聚合酶链反应测量ob mRNA的表达。孵育24小时后,100 nmol/l胰岛素显著增加ob mRNA的表达(与对照组相比增加了21.4倍)。此外,在1-100 nmol/l的范围内,胰岛素以剂量依赖的方式增加ob mRNA的表达。100 nmol/l胰岛素的作用与20%新生牛血清的作用相似。地塞米松(25-1000 nmol/l)也增加ob mRNA的表达(2.5-2.9倍)。地塞米松的作用比胰岛素出现得更快。CGP12177A(1-10 μmol/l)和0.5 mmol/l 8-溴-cAMP没有作用,而0.5 mmol/l 8-溴-cGMP和0.5 mmol/l MIX有刺激作用(ob mRNA分别增加2.8倍和2.4倍)。250 nmol/l地塞米松和0.5 mmol/l MIX的组合对ob mRNA水平没有相加作用。我们目前的数据表明,在这些试剂中,胰岛素是调节ob mRNA表达的最重要因子。