Department of Psychiatry and Behavioral Neurobiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Department of Psychiatry and Behavioral Neurobiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Schizophr Res. 2018 Jul;197:484-491. doi: 10.1016/j.schres.2018.02.010. Epub 2018 Feb 26.
Abnormalities in posttranslational protein modifications (PTMs) that regulate protein targeting, trafficking, synthesis, and function have been implicated in the pathophysiology of schizophrenia. The endoplasmic reticulum (ER) contains specialized machinery that facilitate protein synthesis, ER entry and exit, quality control, and post-translational processing, steps required for protein maturation. Dysregulation of these systems could represent potential mechanisms for abnormalities of neurotransmitter associated proteins in schizophrenia. We hypothesized that expression of ER processing pathways is dysregulated in schizophrenia. We characterized protein and complex expression of essential components from protein folding, ER quality control (ERQC), and ER associated degradation (ERAD) processes in the dorsolateral prefrontal cortex of 12 matched pairs of elderly schizophrenia and comparison subjects. We found increased expression of proteins associated with recognizing and modifying misfolded proteins, including UDP-glucose/glycoprotein glucosyltransferase 2 (UGGT2), ER degradation enhancing alpha-mannosidase like protein 2 (EDEM2), and synoviolin (SYVN1)/HRD1. As SYVN1/HRD1 is a component of the ubiquitin ligase HRD1-SEL1L complex that facilitates ERAD, we immunoprecipitated SEL1L and measured expression of other proteins in this complex. In schizophrenia, SYVN1/HRD1 and OS-9, ERAD promoters, have increased association with SEL1L, while XTP3-B, which can prevent ERAD of substrates, has decreased association. Abnormal expression of proteins associated with ERQC and ERAD suggests dysregulation in ER localized protein processing pathways in schizophrenia. Interestingly, the deficits we found are not in the protein processing machinery itself, but in proteins that recognize and target incompletely or misfolded proteins. These changes may reflect potential mechanisms of abnormal neurotransmitter associated protein expression previously observed in schizophrenia.
蛋白质翻译后修饰(PTMs)的异常会影响蛋白质的靶向、运输、合成和功能,这些异常与精神分裂症的病理生理学有关。内质网(ER)包含专门的机制,可促进蛋白质合成、内质网进入和退出、质量控制和翻译后加工,这些步骤是蛋白质成熟所必需的。这些系统的失调可能代表了精神分裂症中神经递质相关蛋白异常的潜在机制。我们假设 ER 加工途径的表达在精神分裂症中失调。我们描述了 12 对匹配的老年精神分裂症和对照组受试者的背外侧前额叶皮层中与蛋白质折叠、内质网质量控制(ERQC)和内质网相关降解(ERAD)过程相关的关键成分的蛋白质和复合物表达。我们发现,与识别和修饰错误折叠蛋白相关的蛋白表达增加,包括 UDP-葡萄糖/糖蛋白葡萄糖基转移酶 2(UGGT2)、内质网降解增强的α-甘露糖苷酶样蛋白 2(EDEM2)和滑膜蛋白(SYVN1)/HRD1。由于 SYVN1/HRD1 是 HRD1-SEL1L 泛素连接酶复合物的组成部分,可促进 ERAD,我们进行了 SEL1L 的免疫沉淀,并测量了该复合物中其他蛋白的表达。在精神分裂症中,SYVN1/HRD1 和 OS-9(ERAD 启动子)与 SEL1L 的关联增加,而 XTP3-B(可防止底物的 ERAD)的关联减少。与 ERQC 和 ERAD 相关的蛋白表达异常表明,内质网定位的蛋白加工途径在精神分裂症中失调。有趣的是,我们发现的缺陷不是在蛋白质加工机制本身,而是在识别和靶向不完全或错误折叠蛋白的蛋白上。这些变化可能反映了先前在精神分裂症中观察到的异常神经递质相关蛋白表达的潜在机制。