In vitro human embryonic stem cell hematopoiesis mimics MYB-independent yolk sac hematopoiesis.

نویسندگان

  • Stijn Vanhee
  • Katrien De Mulder
  • Yasmine Van Caeneghem
  • Greet Verstichel
  • Nadine Van Roy
  • Björn Menten
  • Imke Velghe
  • Jan Philippé
  • Dominique De Bleser
  • Bart N Lambrecht
  • Tom Taghon
  • Georges Leclercq
  • Tessa Kerre
  • Bart Vandekerckhove
چکیده

Although hematopoietic precursor activity can be generated in vitro from human embryonic stem cells, there is no solid evidence for the appearance of multipotent, self-renewing and transplantable hematopoietic stem cells. This could be due to short half-life of hematopoietic stem cells in culture or, alternatively, human embryonic stem cell-initiated hematopoiesis may be hematopoietic stem cell-independent, similar to yolk sac hematopoiesis, generating multipotent progenitors with limited expansion capacity. Since a MYB was reported to be an excellent marker for hematopoietic stem cell-dependent hematopoiesis, we generated a MYB-eGFP reporter human embryonic stem cell line to study formation of hematopoietic progenitor cells in vitro. We found CD34(+) hemogenic endothelial cells rounding up and developing into CD43(+) hematopoietic cells without expression of MYB-eGFP. MYB-eGFP(+) cells appeared relatively late in embryoid body cultures as CD34(+)CD43(+)CD45(-/lo) cells. These MYB-eGFP(+) cells were CD33 positive, proliferated in IL-3 containing media and hematopoietic differentiation was restricted to the granulocytic lineage. In agreement with data obtained on murine Myb(-/-) embryonic stem cells, bright eGFP expression was observed in a subpopulation of cells, during directed myeloid differentiation, which again belonged to the granulocytic lineage. In contrast, CD14(+) macrophage cells were consistently eGFP(-) and were derived from eGFP-precursors only. In summary, no evidence was obtained for in vitro generation of MYB(+) hematopoietic stem cells during embryoid body cultures. The observed MYB expression appeared late in culture and was confined to the granulocytic lineage.

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عنوان ژورنال:
  • Haematologica

دوره 100 2  شماره 

صفحات  -

تاریخ انتشار 2015