Pollak Daniela, Weitzdoerfer Rachel, Yang Yae-Won, Prast Helmut, Hoeger Harald, Lubec Gert
Department of Pediatrics, Division of Basic Science, Medical University of Vienna, Währinger Gürtel 18, A-1090 Vienna, Austria.
Neurochem Int. 2005 Jan;46(1):19-29. doi: 10.1016/j.neuint.2004.07.003.
The present study uses a proteomic approach to link motor function to cerebellar protein expression in 129X1/SvJ, C57BL/6J and nNOS WT mice. Poor performance on the Rota rod, the standard test for motor coordination, was detected in 129X1/SvJ mice. No gross impairments of neurological, cognitive and behavioural functions were observed. Identification and quantification of 48 proteins revealed reduced expression of calbindin, septin 5 and syntaxin binding protein 1 in 129X1/SvJ. In nNos WT glucose-6-phosphate 1 dehydrogenase X was decreased whereas dihydropyrimidinase-related protein-4 was increased. In C57BL/6J stress-70 protein, alpha enolase, NAD-dependent deacetylase sirtuin 2, septin 2, dihydropyrimidinase-related protein-2 and brain derived neurotrophic factor showed elevated levels. Neurological examination, Rota rod test, Morris Water Maze, Multiple-T-Maze, Open field and Elevated plus-maze were employed to study motor, cognitive and behavioural function. Mice were sacrificed and cerebellar tissue was homogenized. Proteins were extracted and separated on two-dimensional gel electrophoresis with subsequent in-gel digestion followed by mass spectrometrical analysis of peptides (MALDI-TOF/TOF-TOF). Quantification of spots was carried out by specific software. A strong association of impaired motor function with altered cerebellar protein expression of calbindin, septin 5 and syntaxin binding protein 1in 129X1/SvJ was observed and is in agreement with previous observations of motor deficiencies in a calbindin knock-out mouse. These results have to be taken into account when using 129X1/SvJ for biochemical, toxicological or gene targeting experiments as well as when studying the above-mentioned proteins or corresponding pathways and cascades in this mouse strain.
本研究采用蛋白质组学方法,将129X1/SvJ、C57BL/6J和nNOS野生型小鼠的运动功能与小脑蛋白质表达联系起来。在129X1/SvJ小鼠中检测到,其在用于运动协调的标准测试——转棒试验中的表现较差。未观察到神经、认知和行为功能的明显损伤。对48种蛋白质的鉴定和定量分析显示,129X1/SvJ小鼠中钙结合蛋白、septin 5和 syntaxin结合蛋白1的表达降低。在nNOS野生型小鼠中,葡萄糖-6-磷酸1脱氢酶X减少,而二氢嘧啶酶相关蛋白-4增加。在C57BL/6J小鼠中,应激-70蛋白、α烯醇化酶、NAD依赖性脱乙酰酶sirtuin 2、septin 2、二氢嘧啶酶相关蛋白-2和脑源性神经营养因子水平升高。采用神经学检查、转棒试验、莫里斯水迷宫、多重T迷宫、旷场试验和高架十字迷宫来研究运动、认知和行为功能。对小鼠实施安乐死后,将小脑组织匀浆。提取蛋白质并在二维凝胶电泳上进行分离,随后进行胶内消化,接着对肽段进行质谱分析(基质辅助激光解吸电离飞行时间/飞行时间串联质谱)。通过特定软件对斑点进行定量分析。观察到129X1/SvJ小鼠运动功能受损与小脑钙结合蛋白、septin 5和 syntaxin结合蛋白1表达改变之间存在密切关联,这与先前在钙结合蛋白基因敲除小鼠中观察到的运动缺陷一致。在将129X1/SvJ小鼠用于生化、毒理学或基因靶向实验时,以及在研究该小鼠品系中的上述蛋白质或相应途径及级联反应时,必须考虑这些结果。