Udawela M, Money T T, Neo J, Seo M S, Scarr E, Dean B, Everall I P
1] The Florey Institute of Neuroscience and Mental Health, Howard Florey Laboratories, The University of Melbourne, Parkville, VIC, Australia [2] CRC for Mental Health, Carlton South, VIC, Australia.
1] The Florey Institute of Neuroscience and Mental Health, Howard Florey Laboratories, The University of Melbourne, Parkville, VIC, Australia [2] CRC for Mental Health, Carlton South, VIC, Australia [3] Department of Psychiatry, The University of Melbourne, Parkville, VIC, Australia [4] North West Mental Health, Royal Melbourne Hospital, Parkville, VIC, Australia.
Transl Psychiatry. 2015 Aug 4;5(8):e615. doi: 10.1038/tp.2015.108.
Selenium binding protein 1 (SELENBP1) messenger RNA (mRNA) has previously been shown to be upregulated in the brain and blood from subjects with schizophrenia. We aimed to validate these findings in a new cohort using real-time PCR in Brodmann's Area (BA) 9, and to determine the disease specificity of increased SELENBP1 expression by measuring SELENBP1 mRNA in subjects with major depressive disorder and bipolar disorder. We then extended the study to include other cortical regions such as BA8 and BA44. SELENBP1 mRNA was higher in BA9 (P = 0.001), BA8 (P = 0.003) and BA44 (P = 0.0007) from subjects with schizophrenia. Conversely, in affective disorders, there was no significant difference in SELENBP1 mRNA in BA9 (P = 0.67), suggesting that the upregulation may be diagnosis specific. Measurement of SELENBP1 protein levels showed that changes in mRNA did not translate to changes in protein. In addition, chronic treatment of rats with antipsychotics did not significantly affect the expression of Selenbp1 in the cortex (P = 0.24). Our data show that elevated SELENBP1 transcript expression is widespread throughout the prefrontal cortex in schizophrenia, and confirm that this change is a consistent feature of schizophrenia and not a simple drug effect.
先前研究表明,精神分裂症患者大脑和血液中的硒结合蛋白1(SELENBP1)信使核糖核酸(mRNA)表达上调。我们旨在通过对布罗德曼区(BA)9区进行实时聚合酶链反应(PCR),在一个新队列中验证这些发现,并通过测量重度抑郁症和双相情感障碍患者的SELENBP1 mRNA来确定SELENBP1表达增加的疾病特异性。然后,我们将研究扩展到包括BA8和BA44等其他皮质区域。精神分裂症患者的BA9区(P = 0.001)、BA8区(P = 0.003)和BA44区(P = 0.0007)中SELENBP1 mRNA水平较高。相反,在情感障碍患者中,BA9区的SELENBP1 mRNA无显著差异(P = 0.67),这表明这种上调可能具有诊断特异性。SELENBP1蛋白水平的测量结果显示,mRNA的变化并未转化为蛋白质的变化。此外,用抗精神病药物对大鼠进行长期治疗并未显著影响皮质中Selenbp1的表达(P = 0.24)。我们的数据表明,精神分裂症患者前额叶皮质中SELENBP1转录本表达升高是普遍存在的,并证实这种变化是精神分裂症的一个一致特征,而非简单的药物作用。