García-Peral Carlos, Ledesma Martín M, Herrero-Turrión M Javier, Gómez-Nieto Ricardo, Castellano Orlando, López Dolores E
Instituto de Neurociencias de Castilla y León (INCYL), Universidad de Salamanca, 37007 Salamanca, Spain.
Instituto de Investigación Biomédica de Salamanca (IBSAL), 37007 Salamanca, Spain.
Diagnostics (Basel). 2023 Mar 9;13(6):1048. doi: 10.3390/diagnostics13061048.
The GASH/Sal (Genetic Audiogenic Seizure Hamster, Salamanca) is a model of audiogenic seizures with the epileptogenic focus localized in the inferior colliculus (IC). The sound-induced seizures exhibit a short latency (7-9 s), which implies innate protein disturbances in the IC as a basis for seizure susceptibility and generation. Here, we aim to study the protein profile in the GASH/Sal IC in comparison to controls. Protein samples from the IC were processed for enzymatic digestion and then analyzed by mass spectrometry in Data-Independent Acquisition mode. After identifying the proteins using the UniProt database, we selected those with differential expression and performed ontological analyses, as well as gene-protein interaction studies using bioinformatics tools. We identified 5254 proteins; among them, 184 were differentially expressed proteins (DEPs), with 126 upregulated and 58 downregulated proteins, and 10 of the DEPs directly related to epilepsy. Moreover, 12 and 7 proteins were uniquely found in the GASH/Sal or the control. The results indicated a protein profile alteration in the epileptogenic nucleus that might underlie the inborn occurring audiogenic seizures in the GASH/Sal model. In summary, this study supports the use of bioinformatics methods in proteomics to delve into the relationship between molecular-level protein mechanisms and the pathobiology of rodent models of audiogenic seizures.
GASH/Sal(遗传性听源性癫痫仓鼠,萨拉曼卡品系)是一种听源性癫痫模型,其致痫灶定位于下丘(IC)。声音诱发的癫痫发作潜伏期较短(7 - 9秒),这意味着下丘中存在先天性蛋白质紊乱,是癫痫易感性和发作的基础。在此,我们旨在研究GASH/Sal下丘中的蛋白质谱,并与对照组进行比较。对下丘的蛋白质样本进行酶解处理,然后采用数据非依赖采集模式通过质谱分析。使用UniProt数据库鉴定蛋白质后,我们选择那些差异表达的蛋白质并进行本体分析,以及使用生物信息学工具进行基因 - 蛋白质相互作用研究。我们鉴定出5254种蛋白质;其中,184种为差异表达蛋白(DEP),126种上调,58种下调,且10种DEP与癫痫直接相关。此外,分别在GASH/Sal或对照组中独特地发现了12种和7种蛋白质。结果表明致痫核中的蛋白质谱发生改变,这可能是GASH/Sal模型中先天性听源性癫痫发作的基础。总之,本研究支持在蛋白质组学中使用生物信息学方法来深入探究分子水平蛋白质机制与听源性癫痫发作啮齿动物模型病理生物学之间的关系。