Laboratory of Signal Transduction, NIEHS, National Institutes of Heath, Department of Health and Human Services, Research Triangle Park, North Carolina 27709, USA.
J Biol Chem. 2011 Feb 4;286(5):3177-84. doi: 10.1074/jbc.R110.179325. Epub 2010 Dec 13.
Glucocorticoids regulate numerous physiological processes and are mainstays in the treatment of inflammation, autoimmune disease, and cancer. The traditional view that glucocorticoids act through a single glucocorticoid receptor (GR) protein has changed in recent years with the discovery of a large cohort of receptor subtypes arising from alternative processing of the GR gene. These isoforms differ in their expression, gene regulatory, and functional profiles. Post-translational modification of these proteins further expands GR diversity. Here, we discuss the origin and molecular properties of the GR isoforms and their contribution to the sensitivity and specificity of the glucocorticoid response.
糖皮质激素调节着众多的生理过程,是治疗炎症、自身免疫性疾病和癌症的主要药物。近年来,随着糖皮质激素受体(GR)基因的选择性剪接产生大量的受体亚型,糖皮质激素通过单一的 GR 蛋白发挥作用的传统观点发生了改变。这些异构体在表达、基因调控和功能特征上存在差异。这些蛋白的翻译后修饰进一步扩展了 GR 的多样性。本文讨论了 GR 异构体的起源和分子特性,以及它们对糖皮质激素反应的敏感性和特异性的贡献。