Funato Hiromasa, Kobayashi Ayumi, Watanabe Yoshifumi
Division of Neuropsychiatry, Department of Neuroscience, Yamaguchi University School of Medicine, 1-1-1 Minamikogushi, Ube, Yamaguchi 755-8505, Japan.
Brain Res. 2006 Oct 30;1117(1):125-34. doi: 10.1016/j.brainres.2006.08.029. Epub 2006 Sep 7.
The glucocorticoid receptor (GR) is a key regulator of the hypothalamic-pituitary-adrenal (HPA) axis. Mood disorder patients often exhibit abnormalities in this axis. Although the clinical benefit of antidepressants is associated with the normalization of the disturbed HPA activity by enhanced negative feedback of the HPA axis, the precise mechanism remains unknown. In order to examine the effect of antidepressants on the translocation of GR into the nucleus, we performed time-lapse observation on SY5Y cells that had been transiently transfected with plasmids expressing the green fluorescence protein (GFP)-tagged GRalpha. Clomipramine and desipramine facilitated dexamethasone (Dex)-induced GFP-GRalpha nuclear translocation. Coincubation of verapamil, an inhibitor of membrane steroid transporters, showed little or no additive effect on GFP-GRalpha nuclear translocation induced by both Dex and clomipramine. In the absence of Dex, antidepressants did not induce the translocation of GFP-GRalpha into the nucleus. Using real-time PCR, we examined the effect of antidepressants on splicing isoform of GR, GRalpha, and GRbeta in SY5Y and Jurkat cells. Incubation with paroxetine and desipramine for 48 h and 7 days increased GRalpha expression, whereas the expression of GRbeta remained stable. Antidepressants did not alter the expression of SRp30c that is associated with alternative splicing of GR transcript. Thus, antidepressants exert differential effects on the translocation and expression of GR to enhance GR signaling.
糖皮质激素受体(GR)是下丘脑 - 垂体 - 肾上腺(HPA)轴的关键调节因子。情绪障碍患者在该轴上常表现出异常。尽管抗抑郁药的临床益处与通过增强HPA轴的负反馈使紊乱的HPA活性恢复正常有关,但其确切机制仍不清楚。为了研究抗抑郁药对GR向细胞核转位的影响,我们对瞬时转染了表达绿色荧光蛋白(GFP)标记的GRα质粒的SY5Y细胞进行了延时观察。氯米帕明和地昔帕明促进了地塞米松(Dex)诱导的GFP - GRα核转位。膜类固醇转运体抑制剂维拉帕米与Dex和氯米帕明共同孵育,对GFP - GRα核转位几乎没有或没有叠加效应。在没有Dex的情况下,抗抑郁药不会诱导GFP - GRα向细胞核转位。我们使用实时PCR检测了抗抑郁药对SY5Y和Jurkat细胞中GR的剪接异构体GRα和GRβ的影响。用帕罗西汀和地昔帕明孵育48小时和7天可增加GRα的表达,而GRβ的表达保持稳定。抗抑郁药不会改变与GR转录本可变剪接相关的SRp30c的表达。因此,抗抑郁药对GR的转位和表达发挥不同作用以增强GR信号传导。