Evidence for self-maintaining pluripotent murine stem cells in embryoid bodies

Wael A Attia, Osama M Abd El Aziz, Dimitry Spitkovsky, John A Gaspar, Peter Dröge, Frank Suhr, Davood Sabour, Johannes Winkler, Kesavan Meganathan, Smita Jagtap, Markus Khalil, Jürgen Hescheler, [Unbekannt] Konrad Brockmeier, [Unbekannt] Agapios Sachinidis, [Unbekannt] Kurt Pfannkuche

Publication: Contribution to journalJournal articlesResearchpeer-review

Abstract

Pluripotent stem cells have great potential for regenerative medicine; however, their clinical use is associated with a risk of tumor formation. We utilized pluripotent cells expressing green fluorescent protein and puromycin resistance under control of the Oct4 promoter to study the persistence of potential pluripotent cells under embryoid body (EB) culture conditions, which are commonly used to obtain organotypic cells. We found that i.) OCT4-expressing cells dramatically decrease during the first week of differentiation, ii.) the number of OCT4-expressing cells recovers from day 7 on, iii.) the OCT4-expressing cells are similar to embryonic stem cells grown in the presence of leukemia inhibitory factor LIF but express several markers associated with germ cell formation, such as DAZL and STRA-8 and iv.) the persistence of potentially pluripotent cells is independent of supportive cells in EBs. Finally, OCT4-expressing cells, isolated from EBs after 2-month of culture, were further maintained under feeder-free conditions in absence of LIF and continued to express OCT4 in 95 % of the population for at least 36 days. These findings point to an alternative state of stable OCT4 expression. In the frame of the landscape model of differentiation two attractors of pluripotency might be defined based on their different characteristics.

Original languageEnglish
JournalStem cell research
Volume10
Issue number1
Pages (from-to)1-15
Number of pages15
DOIs
Publication statusPublished - 01.02.2014

Research areas and keywords

  • Animals
  • Embryoid Bodies
  • Mice
  • Octamer Transcription Factor-3
  • Pluripotent Stem Cells

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