芳烃受体在多个信号通路的十字路口。

EXS Pub Date : 2009-01-01 DOI:10.1007/978-3-7643-8336-7_9
Ci Ma, Jennifer L Marlowe, Alvaro Puga
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引用次数: 49

摘要

芳烃受体(AHR)长期以来被认为是一种配体激活的转录因子,负责诱导药物代谢酶。早在AHR cDNA序列的第一份报告发表之前,它在细胞功能组合矩阵中的作用就已经确立。直到最近,这种蛋白质的其他功能才开始被认识到,现在很清楚的是,AHR在其在异种酶诱导中众所周知的作用之外,还在其他途径中起作用。外源性配体对这些途径的干扰可能最终解释了这些化合物的毒性。本章重点关注AHR在细胞周期调节、丝裂原活化蛋白激酶级联、分化和凋亡等关键通路中的相互作用。最终,特定AHR配体对生物体生物学的影响将取决于AHR自身与之相互作用的特定细胞和组织中表达的关键途径和蛋白质的环境。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The aryl hydrocarbon receptor at the crossroads of multiple signaling pathways.

The aryl hydrocarbon receptor (AHR) has long been recognized as a ligand-activated transcription factor responsible for the induction of drug-metabolizing enzymes. Its role in the combinatorial matrix of cell functions was established long before the first report of an AHR cDNA sequence was published. It is only recently that other functions of this protein have begun to be recognized, and it is now clear that the AHR also functions in pathways outside of its well-characterized role in xenobiotic enzyme induction. Perturbation of these pathways by xenobiotic ligands may ultimately explain much of the toxicity of these compounds. This chapter focuses on the interactions of the AHR in pathways critical to cell cycle regulation, mitogen-activated protein kinase cascades, differentiation and apoptosis. Ultimately, the effect of a particular AHR ligand on the biology of the organism will depend on the milieu of critical pathways and proteins expressed in specific cells and tissues with which the AHR itself interacts.

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