Bogazzi F, Raggi F, Ultimieri F, Russo D, Campomori A, McKinney J D, Pinchera A, Bartalena L, Martino E
Department of Endocrinology and Metabolism, University of Pisa, Pisa, Italy.
J Endocrinol Invest. 2003 Oct;26(10):972-8. doi: 10.1007/BF03348194.
Polychlorinated biphenyls (PCBs) are environmental contaminants which may affect thyroid function. PCBs may reduce serum thyroid hormone (TH) concentrations by either displacing T4 from TH transport proteins or increasing its hepatic metabolism. The reduced serum T4 causes neurological and growth defects in animals exposed to PCBs during the perinatal period, which can partially be reverted by T4 administration. In addition to a hypothyroid-like syndrome, a direct action of PCBs on TH-sensitive genes has been postulated. In the present study the effects of Aroclor 1254 (ARO), a mixture of PCBs, on transcription of TH-dependent genes were investigated. A reporter plasmid containing the TH-responsive element (TRE) of malic enzyme (ME) gene was used in transient transfections to assess the responsiveness to ARO. ARO (10 microM) reduced the CAT activity by about 50% and competed with T3 to reduce the induction of transcription. Cotransfection of TH receptor (TR) and a wild type TRE was required to reveal ARO inhibitiry effect, which was abolished by a mock reaction not containing TR or by a mutated TRE. ARO reduced the 125I-T3 binding to TR by 30%, but did not affect the interaction of TR with a 32P-labeled TRE in gel shift assay. ARO is likely to produce a conformational change in in vitro translated TR, leading to its increased proteolysis by trypsin. These results demonstrate that ARO interacts with TR, thereby affecting the transcription of TH-sensitive genes, and provide a molecular basis to further explain the complex effects of PCBs on TH disruption.
多氯联苯(PCBs)是可能影响甲状腺功能的环境污染物。多氯联苯可能通过从甲状腺激素转运蛋白上置换T4或增加其肝脏代谢来降低血清甲状腺激素(TH)浓度。血清T4降低会导致围产期接触多氯联苯的动物出现神经和生长缺陷,给予T4可部分逆转这些缺陷。除了类似甲状腺功能减退的综合征外,还推测多氯联苯对甲状腺激素敏感基因有直接作用。在本研究中,研究了多氯联苯混合物Aroclor 1254(ARO)对甲状腺激素依赖性基因转录的影响。在瞬时转染中使用含有苹果酸酶(ME)基因的甲状腺激素反应元件(TRE)的报告质粒来评估对ARO的反应性。ARO(10 microM)使CAT活性降低约50%,并与T3竞争以降低转录诱导。需要共转染甲状腺激素受体(TR)和野生型TRE才能揭示ARO的抑制作用,不含TR的模拟反应或突变的TRE可消除这种作用。ARO使125I-T3与TR的结合减少30%,但在凝胶迁移试验中不影响TR与32P标记的TRE的相互作用。ARO可能会使体外翻译的TR发生构象变化,导致其被胰蛋白酶的蛋白水解增加。这些结果表明ARO与TR相互作用,从而影响甲状腺激素敏感基因的转录,并为进一步解释多氯联苯对甲状腺激素干扰的复杂作用提供了分子基础。