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  4. Differentiation of human embryonic stem cells to HOXA+ hemogenic vasculature that resembles the aorta-gonad-mesonephros
 
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2016
Journal Article
Title

Differentiation of human embryonic stem cells to HOXA+ hemogenic vasculature that resembles the aorta-gonad-mesonephros

Abstract
The ability to generate hematopoietic stem cells from human pluripotent cells would enable many biomedical applications. We find that hematopoietic CD34+ cells in spin embryoid bodies derived from human embryonic stem cells (hESCs) lack HOXA expression compared with repopulation-competent human cord blood CD34+ cells, indicating incorrect mesoderm patterning. Using reporter hESC lines to track the endothelial (SOX17) to hematopoietic (RUNX1C) transition that occurs in development, we show that simultaneous modulation of WNT and ACTIVIN signaling yields CD34+ hematopoietic cells with HOXA expression that more closely resembles that of cord blood. The cultures generate a network of aorta-like SOX17+ vessels from which RUNX1C+ blood cells emerge, similar to hematopoiesis in the aorta-gonad-mesonephros (AGM). Nascent CD34+ hematopoietic cells and corresponding cells sorted from human AGM show similar expression of cell surface receptors, signaling molecules and transcription factors. Our findings provide an approach to mimic in vitro a key early stage in human hematopoiesis for the generation of AGM-derived hematopoietic lineages from hESCs.
Author(s)
Ng, Elisabeth S.
Azzola, Lisa
Bruveris, Freya F.
Calvanese, VIncenzo
Phipson, Belinda
Vlahos, Katerina
Hirst, Claire
Jokubaitis, Vanta J.
Yu, Qing C.
Maksimovic, Jovana
Liebscher, Simone
Januar, Vania
Zhang, Zhen
Williams, Brenda
Conscience, Aude
Durnall, Jennifer
Jackson, Steven
Costa, Magdaline
Elliott, David
Haylock, David N.
Nilsson, Susan K.
Saffery, Richard
Schenke-Layland, Katja  
Oshlack, Alicia
Mikkola, Hanna K.
Stanley, Edouard
Elefanty, Andrew G.
Journal
Nature biotechnology  
DOI
10.1038/nbt.3702
Language
English
Fraunhofer-Institut für Grenzflächen- und Bioverfahrenstechnik IGB  
Keyword(s)
  • differentiation

  • hematopoietic

  • stem cells

  • CD34

  • SOX17+

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