Melbourne Neuropsychiatry Centre, Department of Psychiatry, The University of Melbourne & Melbourne Health, Parkville, VIC, Australia; Melbourne Medical School, Faculty of Medicine Dentistry and Health Sciences, The University of Melbourne, Parkville, VIC, Australia.
Melbourne Neuropsychiatry Centre, Department of Psychiatry, The University of Melbourne & Melbourne Health, Parkville, VIC, Australia; The Cooperative Research Centre (CRC) for Mental Health, Victoria, Australia; Departments of Medical Genetics, Psychiatry, and Physiology & Pharmacology, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
J Psychiatr Res. 2019 Jun;113:51-57. doi: 10.1016/j.jpsychires.2019.03.005. Epub 2019 Mar 8.
A number of recent studies have suggested the ubiquitin proteasome system (UPS) in schizophrenia is dysfunctional. The purpose of this study was to investigate UBE2K, a ubiquitin-conjugating (E2) enzyme within the UPS that has been associated with psychosis symptom severity, in the blood and brain of individuals with schizophrenia. Whole blood and erythrocytes from 128 (71 treatment-resistant schizophrenia, 57 healthy controls) individuals as well as frozen dorsolateral prefrontal cortex (DLPFC) and orbitofrontal cortex (OFC) post-mortem samples from 74 (37 schizophrenia, 37 controls) individuals were obtained. UBE2K gene expression was assayed in whole blood and DLPFC samples, whereas protein levels were assayed in erythrocytes and OFC samples. Elevated levels of UBE2K mRNA were observed in whole blood of individuals with schizophrenia (p = 0.03) but not in the DLPFC, while protein levels were raised in erythrocytes and the OFC (p < 0.001 and p = 0.002 respectively). Findings were not better explained by age, smoking, clozapine plasma levels or duration of illness. Although blood and brain samples were derived from independent samples, our findings suggest peripheral protein levels of UBE2K may serve as a surrogate of brain levels and further supports the notion of UPS dysfunction in schizophrenia. Future studies to determine the pathophysiological effects of elevated UBE2K protein levels in the brain of those with schizophrenia are warranted.
最近的一些研究表明,精神分裂症患者的泛素蛋白酶体系统(UPS)存在功能障碍。本研究旨在研究 UBE2K,这是 UPS 中的一种泛素连接酶(E2),与精神病症状严重程度有关,研究对象为精神分裂症患者的血液和大脑。我们获得了 128 名(71 名治疗抵抗性精神分裂症患者,57 名健康对照者)个体的全血和红细胞,以及 74 名(37 名精神分裂症患者,37 名对照者)个体的冷冻背外侧前额叶皮质(DLPFC)和眶额皮质(OFC)死后样本。我们在全血和 DLPFC 样本中检测了 UBE2K 基因表达,而在红细胞和 OFC 样本中检测了蛋白水平。精神分裂症患者的全血中观察到 UBE2K mRNA 水平升高(p=0.03),但 DLPFC 中没有升高,而红细胞和 OFC 中的蛋白水平升高(p<0.001 和 p=0.002)。这些发现不能用年龄、吸烟、氯氮平血浆水平或疾病持续时间更好地解释。尽管血液和大脑样本来自独立的样本,但我们的研究结果表明,UBE2K 的外周蛋白水平可能是大脑水平的替代物,并进一步支持 UPS 功能障碍在精神分裂症中的观点。未来有必要研究确定那些精神分裂症患者大脑中升高的 UBE2K 蛋白水平的病理生理影响。