Scordino Miriana, Stepanova Polina, Srinivasan Vignesh, Pham Dan Duc, Eriksson Ove, Lalowski Maciej, Mudò Giuseppa, Di Liberto Valentina, Korhonen Laura, Voutilainen Merja H, Lindholm Dan
Department of Biochemistry and Developmental Biology, Medical Faculty, University of Helsinki, Helsinki, Finland.
Biomedicum-2, Minerva Foundation Institute for Medical Research, Helsinki, Finland.
Front Mol Neurosci. 2024 Sep 18;17:1473058. doi: 10.3389/fnmol.2024.1473058. eCollection 2024.
Canopy Homolog 2 (CNPY2) is an endoplasmic reticulum (ER) localized protein belonging to the CNPY gene family. We show here that CNPY2 is protective against ER stress induced by tunicamycin in neuronal cells. Overexpression of CNPY2 enhanced, while downregulation of CNPY2 using shRNA expression, reduced the viability of neuroblastoma cells after tunicamycin. Likewise, recombinant CNPY2 increased survival of cortical neurons in culture after ER stress. CNPY2 reduced the activating transcription factor 6 (ATF6) branch of ER stress and decreased the expression of CCAT/Enhancer-Binding Protein Homologous Protein (CHOP) involved in cell death. Immunostaining using mouse brain sections revealed that CNPY2 is expressed by cortical and striatal neurons and is co-expressed with the transcription factor, COUPTF-interacting protein 2 (CTIP2). In transgenic N171-82Q mice, as a model for Huntington's disease (HD), the number of CNPY2-immunopositive neurons was increased in the cortex together with CTIP2. In the striatum, however, the number of CNPY2 decreased at 19 weeks of age, representing a late-stage of pathology. Striatal cells in culture were shown to be more susceptible to ER stress after downregulation of CNPY2. These results demonstrate that CNPY2 is expressed by corticostriatal neurons involved in the regulation of movement. CNPY2 enhances neuronal survival by reducing ER stress and is a promising factor to consider in HD and possibly in other brain diseases.
冠层同源物2(CNPY2)是一种定位于内质网(ER)的蛋白质,属于CNPY基因家族。我们在此表明,CNPY2对衣霉素诱导的神经元细胞内质网应激具有保护作用。CNPY2的过表达增强了神经母细胞瘤细胞的活力,而使用shRNA表达下调CNPY2则降低了衣霉素处理后神经母细胞瘤细胞的活力。同样,重组CNPY2增加了内质网应激后培养的皮质神经元的存活率。CNPY2减少了内质网应激的激活转录因子6(ATF6)分支,并降低了参与细胞死亡的CCAAT/增强子结合蛋白同源蛋白(CHOP)的表达。使用小鼠脑切片进行免疫染色显示,CNPY2由皮质和纹状体神经元表达,并与转录因子COUPTF相互作用蛋白2(CTIP2)共表达。在作为亨廷顿舞蹈病(HD)模型的转基因N171-82Q小鼠中,皮质中CNPY2免疫阳性神经元的数量与CTIP2一起增加。然而,在纹状体中,CNPY2的数量在19周龄时减少,这代表了病理后期。培养的纹状体细胞在CNPY2下调后对内质网应激更敏感。这些结果表明,CNPY2由参与运动调节的皮质纹状体神经元表达。CNPY2通过减轻内质网应激来提高神经元存活率,是HD以及可能其他脑部疾病中一个值得考虑的有前景的因素。