2-DE proteome analysis of a proliferating and differentiating human neuronal stem cell line (ReNcell VM)

被引:109
作者
Hoffrogge, R
Mikkat, S
Scharf, C
Beyer, S
Christoph, H
Pahnke, J
Mix, E
Berth, M
Uhrmacher, A
Zubrzycki, IZ
Miljan, E
Völker, U
Rolfs, A
机构
[1] Univ Rostock, Dept Neurol, Fac Med, Neurobiol Lab, D-18055 Rostock, Germany
[2] Univ Rostock, Fac Med, Core Facil Proteome Anal, D-18055 Rostock, Germany
[3] Ernst Moritz Arndt Univ Greifswald, Lab Funct Genom, Fac Med, Greifswald, Germany
[4] DECODON GmbH, Greifswald, Germany
[5] Univ Rostock, Dept Comp Sci, D-18055 Rostock, Germany
[6] ReNeuron Ltd, Guildford, Surrey, England
[7] Rzeszow Univ, Fac Nat Sci, Dept Biotechnol, Rzeszow, Poland
[8] Ernst Moritz Arndt Univ Greifswald, Dept Otorhinolaryngol Head & Neck Surg, Greifswald, Germany
关键词
2-DE-map; neuronal stem cells; peroxiredoxin; proteome profiling; transgelin;
D O I
10.1002/pmic.200500556
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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 wen 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.
引用
收藏
页码:1833 / 1847
页数:15
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