Hoffrogge Raimund, Mikkat Stefan, Scharf Christian, Beyer Susanne, Christoph Hilmar, Pahnke Jens, Mix Eilhard, Berth Matthias, Uhrmacher Adelinde, Zubrzycki Igor Z, Miljan Erik, Völker Uwe, Rolfs Arndt
Neurobiological Laboratory, Department of Neurology, Medical Faculty, University of Rostock, Germany.
Proteomics. 2006 Mar;6(6):1833-47. doi: 10.1002/pmic.200500556.
The proteome of a proliferating human stem cell line was analyzed and then utilized to detect stem cell differentiation-associated changes in the protein profile. The analysis was conducted with a stable human fetal midbrain stem cell line (ReNcell VM) that displays the properties of a neural stem cell. Therefore, acquisition of proteomic data should be representative of cultured human neural stem cells (hNSCs) in general. Here we present a 2-DE protein-map of this cell line with annotations of 402 spots representing 318 unique proteins identified by MS. The subsequent proteome profiling of differentiating cells of this stem cell line at days 0, 4 and 7 of differentiation revealed changes in the expression of 49 identified spots that could be annotated to 45 distinct proteins. This differentiation-associated expression pattern was validated by Western blot analysis for transgelin-2, proliferating cell nuclear antigen, as well as peroxiredoxin 1 and 4. The group of regulated proteins also included NudC, ubiquilin-1, STRAP, stress-70 protein, creatine kinase B, glial fibrillary acidic protein and vimentin. Our results reflect the large rearrangement of the proteome during the differentiation process of the stem cells to terminally differentiated neurons and offer the possibility for further characterization of specific targets driving the stem cell differentiation.
对一种增殖的人类干细胞系的蛋白质组进行了分析,然后利用该蛋白质组来检测蛋白质谱中与干细胞分化相关的变化。分析是使用一种稳定的人类胎儿中脑干细胞系(ReNcell VM)进行的,该细胞系具有神经干细胞的特性。因此,蛋白质组学数据的获取总体上应代表培养的人类神经干细胞(hNSCs)。在此,我们展示了该细胞系的二维蛋白质图谱,并对通过质谱鉴定的代表318种独特蛋白质的402个斑点进行了注释。随后对该干细胞系在分化第0、4和7天的分化细胞进行蛋白质组分析,发现49个已鉴定斑点的表达发生了变化,这些斑点可注释为45种不同的蛋白质。通过蛋白质免疫印迹分析对转胶蛋白-2、增殖细胞核抗原以及过氧化物酶1和4进行验证,证实了这种与分化相关的表达模式。受调控的蛋白质组还包括NudC、泛素连接蛋白-1、STRAP、应激70蛋白、肌酸激酶B、胶质纤维酸性蛋白和波形蛋白。我们的结果反映了干细胞向终末分化神经元分化过程中蛋白质组的巨大重排,并为进一步表征驱动干细胞分化的特定靶点提供了可能性。