Department of Veterinary Sciences, University of Pisa, Pisa, Italy.
Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Mol Neurobiol. 2023 Aug;60(8):4336-4358. doi: 10.1007/s12035-023-03347-2. Epub 2023 Apr 24.
The present study, employing a comparative proteomic approach, analyzes the protein profile of pig claustrum (CLA), putamen (PU), and insula (IN). Pig brain is an interesting model whose key translational features are its similarities with cortical and subcortical structures of human brain. A greater difference in protein spot expression was observed in CLA vs PU as compared to CLA vs IN. The deregulated proteins identified in CLA resulted to be deeply implicated in neurodegenerative (i.e., sirtuin 2, protein disulfide-isomerase 3, transketolase) and psychiatric (i.e., copine 3 and myelin basic protein) disorders in humans. Metascape analysis of differentially expressed proteins in CLA vs PU comparison suggested activation of the α-synuclein pathway and L1 recycling pathway corroborating the involvement of these anatomical structures in neurodegenerative diseases. The expression of calcium/calmodulin-dependent protein kinase and dihydropyrimidinase like 2, which are linked to these pathways, was validated using western blot analysis. Moreover, the protein data set of CLA vs PU comparison was analyzed by Ingenuity Pathways Analysis to obtain a prediction of most significant canonical pathways, upstream regulators, human diseases, and biological functions. Interestingly, inhibition of presenilin 1 (PSEN1) upstream regulator and activation of endocannabinoid neuronal synapse pathway were observed. In conclusion, this is the first study presenting an extensive proteomic analysis of pig CLA in comparison with adjacent areas, IN and PUT. These results reinforce the common origin of CLA and IN and suggest an interesting involvement of CLA in endocannabinoid circuitry, neurodegenerative, and psychiatric disorders in humans.
本研究采用比较蛋白质组学方法,分析了猪屏状核(CLA)、壳核(PU)和脑岛(IN)的蛋白质图谱。猪脑是一个有趣的模型,其关键的翻译特征是与人类大脑皮质和皮质下结构相似。CLA 与 PU 相比,CLA 与 IN 相比,蛋白质斑点表达的差异更大。在 CLA 中鉴定出的失调蛋白与人类神经退行性疾病(如 Sirtuin 2、蛋白二硫键异构酶 3、转酮醇酶)和精神疾病(如 Copine 3 和髓鞘碱性蛋白)有很深的关联。CLA 与 PU 比较的差异表达蛋白的 Metascape 分析表明,α-突触核蛋白途径和 L1 回收途径的激活,证实了这些解剖结构参与神经退行性疾病。使用 Western blot 分析验证了与这些途径相关的钙/钙调蛋白依赖性蛋白激酶和二氢嘧啶酶样 2 的表达。此外,还通过 Ingenuity 通路分析对 CLA 与 PU 比较的蛋白质数据集进行了分析,以获得最显著的经典通路、上游调节剂、人类疾病和生物学功能的预测。有趣的是,观察到了 PSEN1 上游调节剂的抑制和内源性大麻素神经元突触途径的激活。总之,这是首次对猪 CLA 与相邻区域 IN 和 PUT 进行比较的广泛蛋白质组学分析。这些结果加强了 CLA 和 IN 的共同起源,并表明 CLA 在内源性大麻素回路、神经退行性和精神疾病中具有有趣的作用。