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The quantitative proteomes of human-induced pluripotent stem cells and embryonic stem cells
被引:100
|作者:
Munoz, Javier
[2
,3
,4
]
Low, Teck Y.
[2
,3
,4
]
Kok, Yee J.
[1
]
Chin, Angela
[1
]
Frese, Christian K.
[2
,3
,4
]
Ding, Vanessa
[1
]
Choo, Andre
[1
]
Heck, Albert J. R.
[2
,3
,4
]
机构:
[1] ASTAR, Bioproc Technol Inst, Stem Cell Grp, Singapore 138668, Singapore
[2] Univ Utrecht, Biomol Mass Spectrometry & Prote Grp, Bijvoet Ctr Biomol Res, Utrecht, Netherlands
[3] Univ Utrecht, Utrecht Inst Pharmaceut Sci, Utrecht, Netherlands
[4] Netherlands Prote Ctr, Utrecht, Netherlands
关键词:
human embryonic stem cells;
human-induced pluripotent stem cells;
proteomics;
quantitation;
HUMAN SOMATIC-CELLS;
PROTEIN-INTERACTION NETWORK;
GENE-EXPRESSION;
HUMAN FIBROBLASTS;
COPY NUMBER;
HUMAN ES;
MOUSE;
DIFFERENTIATION;
METHYLATION;
MEMORY;
D O I:
10.1038/msb.2011.84
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:
Assessing relevant molecular differences between human-induced pluripotent stem cells (hiPSCs) and human embryonic stem cells (hESCs) is important, given that such differences may impact their potential therapeutic use. Controversy surrounds recent gene expression studies comparing hiPSCs and hESCs. Here, we present an in-depth quantitative mass spectrometry-based analysis of hESCs, two different hiPSCs and their precursor fibroblast cell lines. Our comparisons confirmed the high similarity of hESCs and hiPSCS at the proteome level as 97.8% of the proteins were found unchanged. Nevertheless, a small group of 58 proteins, mainly related to metabolism, antigen processing and cell adhesion, was found significantly differentially expressed between hiPSCs and hESCs. A comparison of the regulated proteins with previously published transcriptomic studies showed a low overlap, highlighting the emerging notion that differences between both pluripotent cell lines rather reflect experimental conditions than a recurrent molecular signature. Molecular Systems Biology 7: 550; published online 22 November 2011; doi:10.1038/msb.2011.84
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页数:13
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