Hernández A, St Germain D L, Obregón M J
Unidad de Endocrinología Molecular, Instituto de Investigaciones Biomédicas, Consejo Superior de Investigaciones Científcas, Madrid, Spain.
Endocrinology. 1998 Feb;139(2):634-9. doi: 10.1210/endo.139.2.5734.
The activity of the type III inner ring deiodinase (DIII), which converts T4 and T3 to inactive metabolites, is induced by serum and growth factors in primary cultures of rat brown adipocytes. The contribution of pretranslational mechanisms to this increase in DIII activity was examined in the present studies. DIII mRNA is undetectable in differentiated brown adipocytes when cultured in serum-free medium. However, exposure to epidermal growth factor (EGF), acidic or basic fibroblast growth factors (aFGF or bFGF) increase DIII transcript levels. Lesser inductions are found with platelet-derived growth factor, and insulin-like growth factor I has no effect. Maximal induction of DIII mRNA is obtained after 9 h of exposure to EGF, bFGF, or aFGF at a concentration of 10 ng/ml. The increase in DIII mRNA in response to aFGF, bFGF, and EGF requires gene transcription and protein synthesis, as the inductive effect on mRNA is completely blocked by actinomycin D or cycloheximide. The DIII mRNA half-life is 4 h when stimulated with bFGF and increases to 12 h when 10% serum, EGF, or aFGF is present. In conclusion, EGF, aFGF, and bFGF increase DIII mRNA expression in differentiated brown adipocytes. This effect appears to be exerted at the level of both enhanced transcription and mRNA stabilization.
III型内环脱碘酶(DIII)可将T4和T3转化为无活性代谢产物,在大鼠棕色脂肪细胞原代培养物中,其活性受血清和生长因子诱导。本研究检测了翻译前机制对DIII活性增加的作用。在无血清培养基中培养时,分化的棕色脂肪细胞中检测不到DIII mRNA。然而,暴露于表皮生长因子(EGF)、酸性或碱性成纤维细胞生长因子(aFGF或bFGF)可增加DIII转录水平。血小板衍生生长因子诱导作用较小,胰岛素样生长因子I无作用。在10 ng/ml浓度下,暴露于EGF、bFGF或aFGF 9小时后,可获得DIII mRNA的最大诱导。aFGF、bFGF和EGF引起的DIII mRNA增加需要基因转录和蛋白质合成,因为放线菌素D或环己酰亚胺可完全阻断对mRNA的诱导作用。用bFGF刺激时,DIII mRNA半衰期为4小时,当存在10%血清、EGF或aFGF时,半衰期增加到12小时。总之,EGF、aFGF和bFGF可增加分化的棕色脂肪细胞中DIII mRNA的表达。这种作用似乎在转录增强和mRNA稳定化两个水平上发挥。