雌激素受体和芳烃受体信号通路。

Nuclear receptor signaling Pub Date : 2006-01-01 Epub Date: 2006-07-07 DOI:10.1621/nrs.04016
Jason Matthews, Jan-Ake Gustafsson
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引用次数: 251

摘要

雌激素受体(er)和芳烃受体(AhR)是配体激活的转录因子,分别是核受体和bHLH-PAS超家族的成员。AhR参与外源代谢和介导二恶英样化合物的毒性作用。在AhR和核受体之间观察到串扰,但对内质网信号的研究最为充分。活化的AhR通过多种不同的机制抑制内质网活性,而erα已被报道在AhR信号传导中具有积极作用。在这里,我们将讨论最近的数据揭示二恶英结合的AhR招募erα到AhR调节基因。我们还将考虑ER募集到AhR靶基因对ER和AhR信号传导的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Estrogen receptor and aryl hydrocarbon receptor signaling pathways.

Estrogen receptors (ERs) and the aryl hydrocarbon receptor (AhR) are ligand activated transcription factors and members of the nuclear receptor and bHLH-PAS superfamilies, respectively. AhR is involved in xenobiotic metabolism and in mediating the toxic effects of dioxin-like compounds. Crosstalk has been observed among AhR and nuclear receptors, but has been most well studied with respect to ER signaling. Activated AhR inhibits ER activity through a number of different mechanisms, whereas ERalpha has been reported to have a positive role in AhR signaling. Here we will discuss recent data revealing that dioxin bound AhR recruits ERalpha to AhR regulated genes. We will also consider the implications of ER recruitment to AhR target genes on ER and AhR signaling.

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