Department of Molecular Biomedical Research, VIB, Ghent University, FSVM Building, Technologiepark 927, B9052, Ghent, Belgium.
Traffic. 2012 Mar;13(3):364-74. doi: 10.1111/j.1600-0854.2011.01288.x. Epub 2011 Oct 17.
The glucocorticoid receptor (GR) belongs to the superfamily of steroid receptors and is an important regulator of physiological and metabolic processes. In its inactive state, GR is unbound by ligand and resides in the cytoplasm in a chaperone complex. When it binds glucocorticoids, it is activated and translocates to the nucleus, where it functions as a transcription factor. However, the subcellular localization of GR is determined by the balance between its rates of nuclear import and export. The mechanism of GR nuclear transport has been extensively studied. Originally, it was believed that nuclear import of GR is initiated by dissociation of the chaperone complex in the cytoplasm. However, several studies show that the chaperone machinery is required for nuclear transport of GR. In this review, we summarize the contribution of various chaperone components involved in the nuclear transport of GR and propose an updated model of its nuclear import and export. Moreover, we review the importance of ligand-independent nuclear transport and compare the nuclear transport of GR with that of other steroid receptors.
糖皮质激素受体(GR)属于甾体受体超家族,是生理和代谢过程的重要调节剂。在非活性状态下,GR 无配体结合,位于细胞质中与伴侣复合物结合。当它与糖皮质激素结合时,它被激活并易位到细胞核,在那里它作为转录因子发挥作用。然而,GR 的亚细胞定位取决于其核输入和输出的速率之间的平衡。GR 核转运的机制已得到广泛研究。最初,人们认为 GR 的核输入是由细胞质中伴侣复合物的解离启动的。然而,多项研究表明,伴侣机制对于 GR 的核转运是必需的。在这篇综述中,我们总结了参与 GR 核转运的各种伴侣成分的贡献,并提出了其核输入和输出的更新模型。此外,我们还回顾了非配体依赖性核转运的重要性,并比较了 GR 与其他甾体受体的核转运。