Fries Gabriel R, Gassen Nils C, Schmidt Ulrike, Rein Theo
Department of Translational Research in Psychiatry, Max Planck Institute of Psychiatry, Munich, Germany.
Curr Mol Pharmacol. 2015;9(2):126-40. doi: 10.2174/1874467208666150519114435.
The immunophilin FK506 binding protein 51 (FKBP51) has emerged as one of the most intensely investigated proteins in stress-related mental disorders. It was originally characterized as Hsp90 cochaperone and part of the receptor-chaperone heterocomplex that governs the activity of steroid receptors. It turned out that the presence of FKBP51 in this heterocomplex leads to diminished activity of the corticosteroid receptors. In particular, based on its inhibitory action on the glucocorticoid receptor (GR), FKBP51 was included in a candidate gene approach to discover gene polymorphisms that might be relevant for the development and treatment of major depression. The discovery that polymorphisms in the gene coding for FKBP51 were linked to the treatment response of depressed patients intensified the research on the role of FKBP51 in stress-related diseases worldwide. It has become evident that FKBP51 is not only a regulator of GR action, but also a GR target. The function of this ultrashort intracellular feedback loop is critically important for cellular and physiological stress regulation as it does not only calibrate the function of GR, but also the levels of FKBP51. Given the pleiotropic functions of FKBP51, its levels might be equally important for mental disorders as GR function and hence for the development of potential FKBP51 drug targets.
亲免素FK506结合蛋白51(FKBP51)已成为应激相关精神障碍中研究最为深入的蛋白之一。它最初被表征为Hsp90共伴侣蛋白,是调控类固醇受体活性的受体 - 伴侣异源复合物的一部分。结果发现,该异源复合物中FKBP51的存在会导致皮质类固醇受体活性降低。特别是,基于其对糖皮质激素受体(GR)的抑制作用,FKBP51被纳入候选基因研究方法,以发现可能与重度抑郁症的发生和治疗相关的基因多态性。编码FKBP51的基因多态性与抑郁症患者治疗反应相关这一发现,加强了全球范围内对FKBP51在应激相关疾病中作用的研究。很明显,FKBP51不仅是GR作用的调节因子,也是GR的靶点。这种超短细胞内反馈回路的功能对于细胞和生理应激调节至关重要,因为它不仅校准GR的功能,还校准FKBP51的水平。鉴于FKBP51的多效性功能,其水平对于精神障碍可能与GR功能同样重要,因此对于潜在FKBP51药物靶点的开发也很重要。