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

Authors :
Yasmine Van Caeneghem
Bart Vandekerckhove
Bart N. Lambrecht
Björn Menten
Stijn Vanhee
Tessa Kerre
Georges Leclercq
Katrien De Mulder
Imke Velghe
Greet Verstichel
Tom Taghon
Jan Philippé
Nadine Van Roy
Dominique De Bleser
Source :
HAEMATOLOGICA
Publication Year :
2014

Abstract

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.

Details

ISSN :
15928721 and 03906078
Volume :
100
Issue :
2
Database :
OpenAIRE
Journal :
Haematologica
Accession number :
edsair.doi.dedup.....03259190e21eb1f11699d8bc622ff994