Differentiation-independent fluctuation of pluripotency-related transcription factors and other epigenetic markers in embryonic stem cell colonies
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
21609209
PubMed Central
PMC3295859
DOI
10.1089/scd.2011.0085
Knihovny.cz E-zdroje
- MeSH
- antigen Ki-67 metabolismus MeSH
- buněčná diferenciace * MeSH
- buněčné jádro genetika metabolismus MeSH
- embryonální kmenové buňky cytologie metabolismus MeSH
- epigeneze genetická MeSH
- FRAP MeSH
- G2 fáze MeSH
- histony metabolismus MeSH
- homeodoménové proteiny genetika metabolismus MeSH
- konfokální mikroskopie MeSH
- kultivované buňky MeSH
- lysin metabolismus MeSH
- metylace MeSH
- myši MeSH
- nanog MeSH
- nika kmenových buněk MeSH
- oktamerní transkripční faktor 3 genetika metabolismus MeSH
- pluripotentní kmenové buňky cytologie metabolismus MeSH
- protoonkogenní proteiny c-myc genetika metabolismus MeSH
- western blotting MeSH
- zelené fluorescenční proteiny genetika metabolismus MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antigen Ki-67 MeSH
- histony MeSH
- homeodoménové proteiny MeSH
- lysin MeSH
- Myc protein, mouse MeSH Prohlížeč
- Nanog protein, mouse MeSH Prohlížeč
- nanog MeSH
- oktamerní transkripční faktor 3 MeSH
- protoonkogenní proteiny c-myc MeSH
- zelené fluorescenční proteiny MeSH
Embryonic stem cells (ESCs) maintain their pluripotency through high expression of pluripotency-related genes. Here, we show that differing levels of Oct4, Nanog, and c-myc proteins among the individual cells of mouse ESC (mESC) colonies and fluctuations in these levels do not disturb mESC pluripotency. Cells with strong expression of Oct4 had low levels of Nanog and c-myc proteins and vice versa. In addition, cells with high levels of Nanog tended to occupy interior regions of mESC colonies. In contrast, peripherally positioned cells within colonies had dense H3K27-trimethylation, especially at the nuclear periphery. We also observed distinct levels of endogenous and exogenous Oct4 in particular cell cycle phases. The highest levels of Oct4 occurred in G2 phase, which correlated with the pKi-67 nuclear pattern. Moreover, the Oct4 protein resided on mitotic chromosomes. We suggest that there must be an endogenous mechanism that prevents the induction of spontaneous differentiation, despite fluctuations in protein levels within an mESC colony. Based on the results presented here, it is likely that cells within a colony support each other in the maintenance of pluripotency.
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