Department of Psychology and Behavioral Neuroscience, The University of Alabama at Birmingham, 3811 O'Hara Street BST W1651, Pittsburgh, PA, 15213, USA.
Department of Psychiatry and Behavioral Neurobiology, The University of Alabama at Birmingham, Pittsburgh, USA.
J Neural Transm (Vienna). 2021 May;128(5):701-709. doi: 10.1007/s00702-021-02333-z. Epub 2021 Apr 22.
Schizophrenia susceptibility factor dysbindin-1 is associated with cognitive processes. Downregulated dysbindin-1 expression is associated with lower expression of copper transporters ATP7A and CTR1, required for copper transport to the central nervous system. We measured dysbindin-1 isoforms-1A and -1BC, CTR1, and ATP7A via Western blots of the postmortem dorsolateral prefrontal cortex (DLPFC) of schizophrenia subjects (n = 28) and matched controls (n = 14). In addition, we subdivided the schizophrenia group by treatment status and comorbidity of alcohol use disorder (AUD) and assessed the relationships between proteins. Schizophrenia subjects exhibited similar protein levels to that of controls, with no effect of antipsychotic treatment. We observed a shift towards more dysbindin-1A expression in schizophrenia, as revealed by the ratio of dysbindin-1 isoforms. Dysbindin-1A expression was negatively correlated with ATP7A in schizophrenia, with no correlation present in controls. AUD subjects exhibited less dysbindin-1BC and CTR1 than those without AUD. Our results, taken together with previous data, suggest that alterations in dysbindin-1 and copper transporters are brain-region specific. For example, protein levels of ATP7A, dysbindin 1BC, and CTR1 are lower in the substantia nigra in schizophrenia subjects. AUD in the DLPFC was associated with lower protein levels of dysbindin-1 and CTR1. Changes in dysbindin-1 isoform ratio and relationships appear to be prevalent in the disease, potentially impacting symptomology.
精神分裂症易感因子 dysbindin-1 与认知过程有关。下调 dysbindin-1 的表达与铜转运到中枢神经系统所需的铜转运体 ATP7A 和 CTR1 的表达降低有关。我们通过 Western blot 测量了精神分裂症患者(n=28)和匹配对照组(n=14)死后背外侧前额叶皮质(DLPFC)中的 dysbindin-1 异构体-1A 和-1BC、CTR1 和 ATP7A。此外,我们根据治疗状况和酒精使用障碍(AUD)的合并症对精神分裂症组进行了细分,并评估了蛋白质之间的关系。精神分裂症患者的蛋白水平与对照组相似,抗精神病药物治疗没有影响。我们观察到精神分裂症中 dysbindin-1A 的表达向更多方向转移,这反映在 dysbindin-1 异构体的比例上。精神分裂症中 dysbindin-1A 的表达与 ATP7A 呈负相关,而对照组中没有相关性。有 AUD 的患者的 dysbindin-1BC 和 CTR1 表达低于没有 AUD 的患者。我们的结果与以前的数据一起表明,dysbindin-1 和铜转运体的改变是大脑区域特异性的。例如,在精神分裂症患者的黑质中,ATP7A、dysbindin 1BC 和 CTR1 的蛋白水平较低。AUD 在 DLPFC 与 dysbindin-1 和 CTR1 蛋白水平降低有关。dysbindin-1 异构体比例的变化和关系似乎在疾病中普遍存在,可能会影响症状。