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

• Published in: Nature biotechnology Vol. 34; no. 11; pp. 1168 - 1179
• Main Authors: Ng, Elizabeth 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 A, Stanley, Edouard G, Elefanty, Andrew G
• Format: Journal Article
• Language: English
• Published: 01-11-2016
• ISSN: 1087-0156
• DOI: 10.1038/nbt.3702

The ability to generate hematopoietic stem cells from human pluripotent cells would enable many biomedical applications. We find that hematopoietic CD34 super(+) cells in spin embryoid bodies derived from human embryonic stem cells (hESCs) lack HOXA expression compared with repopulation-competent human cord blood CD34 super(+) 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 super(+) hematopoietic cells with HOXA expression that more closely resembles that of cord blood. The cultures generate a network of aorta-like SOX17 super(+) vessels from which RUNX1C super(+) blood cells emerge, similar to hematopoiesis in the aorta-gonad-mesonephros (AGM). Nascent CD34 super(+) 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.