Comparative proteomic analysis reveals differential expression of Hsp25 following the directed differentiation of mouse embryonic stem cells

被引:46
作者
Battersby, Alysia
Jones, Robert D.
Lilley, Kathryn S.
McFarlane, Ramsay J.
Braig, Henk R.
Allen, Nicholas D.
Wakeman, Jane A.
机构
[1] Univ Wales Bangor, NW Canc Res Fund Inst, Bangor LL57 2UW, Gwynedd, Wales
[2] Cardiff Univ, Sch Biosci, Cardiff CF10 3US, Wales
[3] Univ Cambridge, Cambridge Ctr Proteom, Dept Biochem, Cambridge CB1 1QW, England
[4] Univ Coll N Wales, Sch Biol Sci, Bangor LL57 2UW, Gwynedd, Wales
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2007年 / 1773卷 / 02期
基金
英国生物技术与生命科学研究理事会;
关键词
mouse embryonic stem cell; neural differentiation; Hsp25; protein;
D O I
10.1016/j.bbamcr.2006.08.030
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Murine embryonic stem (ES) cells can be committed to neural differentiation with high efficiency in culture through the use of feeder- and serum-free media. This system is proving to be an excellent model to study processes involved in ES cell commitment to neural cell fate. We used this approach to generate neurogenic embryoid bodies (NEBs) in a serum-free culture system to perforin proteomic analysis of soluble fractions and identify early changes in protein expression as ES cells differentiate. Ten candidate proteins were altered significantly in expression levels. One of the most significant alterations was for the small heat shock protein Hsp25. Three species of Hsp25 are detected in ES cells, and this expression pattern changes during the first 24 h of differentiation until expression is decreased to levels that are barely detectable at 4 days following differentiation. We used immunofluorescence studies to confirm that following ES cell differentiation, expression of Hsp25 becomes excluded from neural precursors as well as other differentiating cells, making it a potentially useful marker of early ES cell differentiation. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:147 / 156
页数:10
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