Hadjighassem Mahmoud R, Austin Mark C, Szewczyk Bernadeta, Daigle Mireille, Stockmeier Craig A, Albert Paul R
Ottawa Health Research Institute (Neuroscience), University of Ottawa, Ottawa, Ontario K1H-8M5, Canada.
Biol Psychiatry. 2009 Aug 1;66(3):214-22. doi: 10.1016/j.biopsych.2009.02.033. Epub 2009 May 7.
Altered expression of serotonin-1A (5-HT1A) receptors, both presynaptic in the raphe nuclei and post-synaptic in limbic and cortical target areas, has been implicated in mood disorders such as major depression and anxiety. Within the 5-HT1A receptor gene, a powerful dual repressor element (DRE) is regulated by two protein complexes: Freud-1/CC2D1A and a second, unknown repressor. Here we identify human Freud-2/CC2D1B, a Freud-1 homologue, as the second repressor.
Freud-2 distribution was examined with Northern and Western blot, reverse transcriptase polymerase chain reaction, and immunohistochemistry/immunofluorescence; Freud-2 function was examined by electrophoretic mobility shift, reporter assay, and Western blot.
Freud-2 RNA was widely distributed in brain and peripheral tissues. Freud-2 protein was enriched in the nuclear fraction of human prefrontal cortex and hippocampus but was weakly expressed in the dorsal raphe nucleus. Freud-2 immunostaining was co-localized with 5-HT1A receptors, neuronal and glial markers. In prefrontal cortex, Freud-2 was expressed at similar levels in control and depressed male subjects. Recombinant hFreud-2 protein bound specifically to 5' or 3' human DRE adjacent to the Freud-1 site. Human Freud-2 showed strong repressor activity at the human 5-HT1A or heterologous promoter in human HEK-293 5-HT1A-negative cells and neuronal SK-N-SH cells, a model of postsynaptic 5-HT1A receptor-positive cells. Furthermore, small interfering RNA knockdown of endogenous hFreud-2 expression de-repressed 5-HT1A promoter activity and increased levels of 5-HT1A receptor protein in SK-N-SH cells.
Human Freud-2 binds to the 5-HT1A DRE and represses the human 5-HT1A receptor gene to regulate its expression in non-serotonergic cells and neurons.
血清素1A(5-HT1A)受体的表达改变,在中缝核中为突触前表达,在边缘和皮质靶区为突触后表达,这与诸如重度抑郁和焦虑等情绪障碍有关。在5-HT1A受体基因内,一个强大的双重抑制元件(DRE)受两种蛋白质复合物调控:Freud-1/CC2D1A和另一种未知的抑制因子。在此,我们鉴定出人类Freud-2/CC2D1B(Freud-1的同源物)为第二种抑制因子。
采用Northern印迹法、Western印迹法、逆转录聚合酶链反应以及免疫组织化学/免疫荧光法检测Freud-2的分布;通过电泳迁移率变动分析、报告基因检测和Western印迹法检测Freud-2的功能。
Freud-2 RNA广泛分布于脑和外周组织中。Freud-2蛋白在人类前额叶皮质和海马体的核部分中富集,但在中缝背核中表达较弱。Freud-2免疫染色与5-HT1A受体、神经元和胶质细胞标志物共定位。在前额叶皮质中,Freud-2在对照男性受试者和抑郁男性受试者中的表达水平相似。重组hFreud-2蛋白特异性结合至Freud-1位点附近的5'或3'人类DRE。人类Freud-2在人类HEK-293 5-HT1A阴性细胞和神经元SK-N-SH细胞(一种突触后5-HT1A受体阳性细胞模型)中的人类5-HT1A或异源启动子处表现出强大的抑制活性。此外,内源性hFreud-2表达的小干扰RNA敲低解除了对5-HT1A启动子活性的抑制,并增加了SK-N-SH细胞中5-HT1A受体蛋白的水平。
人类Freud-2与5-HT1A DRE结合并抑制人类5-HT1A受体基因,以调节其在非5-羟色胺能细胞和神经元中的表达。