Ernst Carl, Deleva Vesselina, Deng Xiaoming, Sequeira Adolfo, Pomarenski Amanda, Klempan Tim, Ernst Neil, Quirion Remi, Gratton Alain, Szyf Moshe, Turecki Gustavo
Departments ofNeurology and Neurosurgery, Douglas Hospital Research Institute, Montreal, QC H4H 1R3, Canada.
Arch Gen Psychiatry. 2009 Jan;66(1):22-32. doi: 10.1001/archpsyc.66.1.22.
Although most of the effort to understand the neurobiology of depressive states and suicide has focused on neuronal processes, recent studies suggest that astroglial dysfunction may play an important role. A truncated variant of the tropomyosin-related kinase B (TrkB.T1) is expressed in astrocytes, and brain-derived neurotrophic factor-TrkB signaling has been linked to mood disorders.
To test the hypothesis that TrkB.T1 expression is downregulated in suicide completers and that this downregulation is mediated by an epigenetic process.
Postmortem case-control study. Patients, Setting, and
Thirty-nine French Canadian men underwent screening at the Douglas Hospital Research Institute using the HG-U133 plus 2 microarray chip. Nine frontal cortical regions and the cerebellum were assessed using a microarray screening approach for extreme expression differences across subjects and a conventional screening approach. Results were validated by quantitative polymerase chain reaction and Western blot analyses. Animal experiments were performed to control for drug and alcohol effects. Genetic and epigenetic studies were performed by means of direct sequencing and bisulfite mapping.
We found that 10 of 28 suicide completers (36%) demonstrated significant decreases in different probe sets specific to TrkB.T1 in Brodmann areas 8 and 9. These findings were generalizable to other frontal regions but not to the cerebellum. The decrease in TrkB expression was specific to the T1 splice variant. Our results were not accounted for by substance comorbidity or by reduction in astrocyte number. We found no effect of genetic variation in a 2500-base pair promoter region or at relevant splice junctions; however, we detected an effect of methylation state at particular CpG dinucleotides on TrkB.T1 expression.
A reduction of TrkB.T1 expression in the frontal cortex of a subpopulation of suicide completers is associated with the methylation state of the promoter region.
尽管大多数旨在了解抑郁状态和自杀的神经生物学机制的研究都聚焦于神经元过程,但最近的研究表明,星形胶质细胞功能障碍可能起重要作用。原肌球蛋白相关激酶B(TrkB.T1)的截短变体在星形胶质细胞中表达,且脑源性神经营养因子-TrkB信号传导与情绪障碍有关。
验证自杀完成者中TrkB.T1表达下调且这种下调由表观遗传过程介导这一假说。
尸检病例对照研究。
患者、研究地点及主要观察指标:39名法裔加拿大男性在道格拉斯医院研究所使用HG-U133 plus 2芯片进行筛查。采用微阵列筛选方法评估九个额叶皮质区域和小脑在受试者间的极端表达差异,并采用传统筛选方法进行评估。结果通过定量聚合酶链反应和蛋白质印迹分析进行验证。进行动物实验以控制药物和酒精的影响。通过直接测序和亚硫酸氢盐定位进行遗传和表观遗传学研究。
我们发现,28名自杀完成者中有10名(36%)在布罗德曼8区和9区中,与TrkB.T1特异性相关的不同探针组出现显著下降。这些发现可推广至其他额叶区域,但不适用于小脑。TrkB表达的下降特定于T1剪接变体。我们的结果不能用物质合并症或星形胶质细胞数量减少来解释。我们在2500个碱基对的启动子区域或相关剪接位点未发现遗传变异的影响;然而,我们检测到特定CpG二核苷酸的甲基化状态对TrkB.T1表达有影响。
自杀完成者亚组额叶皮质中TrkB.T1表达的降低与启动子区域的甲基化状态有关。