Hernández A, Obregón M J
Unidad de Endocrinología Molecular, Instituto de Investigaciones Biomédicas, Consejo Superior de Investigaciones Cientificas, Madrid, Spain.
Endocrinology. 1995 Oct;136(10):4543-50. doi: 10.1210/endo.136.10.7664675.
We found low T3 concentrations in rat brown adipocytes differentiated in vitro. This might be due to the high metabolic rate of T3, possibly caused by elevated type III iodothyronine 5-deiodinase activity (5DIII), induced by serum growth factors. We tested the ability of several growth factors to induce 5DIII activity. Epidermal growth factor and basic and acidic fibroblast growth factors produced a strong induction of 5DIII activity (25, 45-, and 50-fold, respectively). This process required gene transcription and de novo protein synthesis. The half-life of 5DIII was approximately 3 h. Heparin was required for full acidic fibroblast growth factor activity. Platelet-derived growth factor, vasopressin, and insulin-like growth factor-I induced lower 5DIII activities (3- to 6-fold). Vasopressin amplified basic fibroblast growth factor and epidermal growth factor inductions when used at submaximal doses. We found a Km of 22.5 nM using T3 as substrate. Although brown adipose tissue has undetectable 5DIII activities in vivo, the present data explain the low T3 concentrations found in cultured rat brown adipocytes and suggest that growth factors, by stimulating 5DIII, may lead to low T3 concentrations and indirectly inhibit the expression of some genes regulated by T3, e.g. the rat uncoupling protein.
我们发现体外分化的大鼠棕色脂肪细胞中三碘甲状腺原氨酸(T3)浓度较低。这可能是由于T3代谢率高,可能是由血清生长因子诱导的III型碘甲状腺原氨酸5-脱碘酶(5DIII)活性升高所致。我们测试了几种生长因子诱导5DIII活性的能力。表皮生长因子、碱性和酸性成纤维细胞生长因子对5DIII活性有强烈诱导作用(分别为25倍、45倍和50倍)。这个过程需要基因转录和从头合成蛋白质。5DIII的半衰期约为3小时。完全发挥酸性成纤维细胞生长因子的活性需要肝素。血小板衍生生长因子、血管加压素和胰岛素样生长因子-I诱导的5DIII活性较低(3至6倍)。当以亚最大剂量使用时,血管加压素可增强碱性成纤维细胞生长因子和表皮生长因子的诱导作用。以T3为底物时,我们测得米氏常数(Km)为22.5 nM。尽管棕色脂肪组织在体内5DIII活性检测不到,但目前的数据解释了培养的大鼠棕色脂肪细胞中T3浓度较低的现象,并表明生长因子通过刺激5DIII可能导致T3浓度降低,并间接抑制一些受T3调控的基因的表达,例如大鼠解偶联蛋白。