Viguerie Nathalie, Millet Laurence, Avizou Sebastien, Vidal Hubert, Larrouy Dominique, Langin Dominique
INSERM Unit 317, Institut Louis Bugnard, Université Paul Sabatier, Hôpital Rangueil, 31403 Toulouse Cedex 4, France.
J Clin Endocrinol Metab. 2002 Feb;87(2):630-4. doi: 10.1210/jcem.87.2.8200.
Thyroid hormones are key regulators of metabolism. In adipose tissue, changes in thyroid status result in alterations of lipolytic capacity. The effects of these hormones are mediated by thyroid hormone receptors that modulate gene transcription. Very few target genes have been identified in adipose tissue. To investigate the effect of T(3) on gene expression in human adipocytes, primary cultures of human sc adipose tissue explants were treated with T(3). (32)P-labeled cDNA probes prepared from isolated adipocyte total RNA were hybridized to cDNA arrays representing 1,176 genes. Among the statistically significant variations in mRNA levels with more than 1.3-fold difference, 13 and 6 genes were positively and negatively regulated, respectively (n = 3). The genes encoded proteins that were involved in signal transduction, lipid metabolism, apoptosis, and inflammatory response. Using RT-competitive PCR, we showed a down-regulation of phosphodiesterase 3B, alpha(2A)-adrenergic receptor, and G protein alpha(i2) subunit mRNAs, and an up-regulation of beta(2)-adrenergic receptor mRNA. These regulations may explain the T(3)-mediated increase in catecholamine-induced lipolysis. The down-regulation of sterol regulatory element binding protein-1c, a transcription factor controlling lipogenic gene expression, may constitute a link between thyrotoxicosis and insulin resistance. Thus, these data suggest that T(3) modulates expression of genes with a wide range of function in human adipose tissue.
甲状腺激素是新陈代谢的关键调节因子。在脂肪组织中,甲状腺状态的改变会导致脂解能力的变化。这些激素的作用是由调节基因转录的甲状腺激素受体介导的。在脂肪组织中已鉴定出的靶基因非常少。为了研究T3对人脂肪细胞基因表达的影响,用人皮下脂肪组织外植体的原代培养物进行T3处理。从分离的脂肪细胞总RNA制备的(32)P标记的cDNA探针与代表1176个基因的cDNA阵列杂交。在mRNA水平上具有超过1.3倍差异的统计学显著变化中,分别有13个和6个基因受到正向和负向调节(n = 3)。这些基因编码参与信号转导、脂质代谢、细胞凋亡和炎症反应的蛋白质。使用RT竞争PCR,我们发现磷酸二酯酶3B、α(2A)-肾上腺素能受体和G蛋白α(i2)亚基的mRNA表达下调,而β(2)-肾上腺素能受体mRNA表达上调。这些调节可能解释了T3介导的儿茶酚胺诱导的脂解增加。固醇调节元件结合蛋白-1c是一种控制脂肪生成基因表达的转录因子,其表达下调可能构成甲状腺毒症与胰岛素抵抗之间的联系。因此,这些数据表明T3调节人脂肪组织中具有广泛功能的基因的表达。