Choi Kwang, Le Thien, Xing Guoqiang, Johnson Luke R, Ursano Robert J
Department of Psychiatry, Center for the Study of Traumatic Stress, Uniformed Services University of Health Sciences Bethesda, MD, USA.
Front Behav Neurosci. 2011 Jul 28;5:46. doi: 10.3389/fnbeh.2011.00046. eCollection 2011.
Suicide is a serious public health issue that results from an interaction between multiple risk factors including individual vulnerabilities to complex feelings of hopelessness, fear, and stress. Although kinase genes have been implicated in fear and stress, including the consolidation and extinction of fearful memories, expression profiles of those genes in the brain of suicide victims are less clear. Using gene expression microarray data from the Online Stanley Genomics Database and a quantitative PCR, we investigated the expression profiles of multiple kinase genes including the calcium calmodulin-dependent kinase (CAMK), the cyclin-dependent kinase, the mitogen-activated protein kinase (MAPK), and the protein kinase C (PKC) in the prefrontal cortex (PFC) of mood disorder patients died with suicide (N = 45) and without suicide (N = 38). We also investigated the expression pattern of the same genes in the PFC of developing humans ranging in age from birth to 49 year (N = 46). The expression levels of CAMK2B, CDK5, MAPK9, and PRKCI were increased in the PFC of suicide victims as compared to non-suicide controls (false discovery rate, FDR-adjusted p < 0.05, fold change >1.1). Those genes also showed changes in expression pattern during the postnatal development (FDR-adjusted p < 0.05). These results suggest that multiple kinase genes undergo age-dependent changes in normal brains as well as pathological changes in suicide brains. These findings may provide an important link to protein kinases known to be important for the development of fear memory, stress associated neural plasticity, and up-regulation in the PFC of suicide victims. More research is needed to better understand the functional role of these kinase genes that may be associated with the pathophysiology of suicide.
自杀是一个严重的公共卫生问题,它源于多种风险因素之间的相互作用,这些因素包括个体对绝望、恐惧和压力等复杂情绪的易感性。尽管激酶基因与恐惧和压力有关,包括恐惧记忆的巩固和消退,但这些基因在自杀受害者大脑中的表达谱尚不清楚。利用来自在线斯坦利基因组数据库的基因表达微阵列数据和定量PCR,我们研究了多种激酶基因的表达谱,包括钙调蛋白依赖性激酶(CAMK)、细胞周期蛋白依赖性激酶、丝裂原活化蛋白激酶(MAPK)和蛋白激酶C(PKC),这些基因存在于自杀身亡的情绪障碍患者(N = 45)和未自杀的情绪障碍患者(N = 38)的前额叶皮层(PFC)中。我们还研究了年龄从出生到49岁的发育中人类(N = 46)的PFC中相同基因的表达模式。与非自杀对照组相比,自杀受害者PFC中CAMK2B、CDK5、MAPK9和PRKCI的表达水平升高(错误发现率,FDR校正p < 0.05,倍数变化>1.1)。这些基因在出生后发育过程中也显示出表达模式的变化(FDR校正p < 0.05)。这些结果表明,多种激酶基因在正常大脑中经历年龄依赖性变化,在自杀大脑中也经历病理变化。这些发现可能为已知对恐惧记忆发展、与压力相关的神经可塑性以及自杀受害者PFC上调很重要的蛋白激酶提供重要联系。需要更多研究来更好地理解这些可能与自杀病理生理学相关的激酶基因的功能作用。