SOX17 integrates HOXA and arterial programs in hemogenic endothelium to drive definitive lympho-myeloid hematopoiesis

• Published in: Cell reports (Cambridge) Vol. 34; no. 7; p. 108758
• Main Authors: Jung, Ho Sun, Uenishi, Gene, Park, Mi Ae, Liu, Peng, Suknuntha, Kran, Raymond, Matthew, Choi, Yoon Jung, Thomson, James A., Ong, Irene M., Slukvin, Igor I.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 16.02.2021
• Subjects: Animals; arterial hemogenic endothelium; CDX2; Cell Differentiation - physiology; Embryonic Stem Cells - cytology; Embryonic Stem Cells - metabolism; hematopietic development; Hematopoiesis - genetics; hemogenic endothleium specification; Homeodomain Proteins - metabolism; HOXA; human pluripotent stem cells; Humans; Induced Pluripotent Stem Cells - cytology; Induced Pluripotent Stem Cells - metabolism; NOTCH signaling; SOX17; SOXF Transcription Factors - metabolism; NOTCH signaling; HOXA; SOX17; CDX2; arterial hemogenic endothelium; human pluripotent stem cells; hemogenic endothleium specification; hematopietic development
• ISSN: 2211-1247; 2211-1247
• DOI: 10.1016/j.celrep.2021.108758

SOX17 has been implicated in arterial specification and the maintenance of hematopoietic stem cells (HSCs) in the murine embryo. However, knowledge about molecular pathways and stage-specific effects of SOX17 in humans remains limited. Here, using SOX17-knockout and SOX17-inducible human pluripotent stem cells (hPSCs), paired with molecular profiling studies, we reveal that SOX17 is a master regulator of HOXA and arterial programs in hemogenic endothelium (HE) and is required for the specification of HE with robust lympho-myeloid potential and DLL4+CXCR4+ phenotype resembling arterial HE at the sites of HSC emergence. Along with the activation of NOTCH signaling, SOX17 directly activates CDX2 expression, leading to the upregulation of the HOXA cluster genes. Since deficiencies in HOXA and NOTCH signaling contribute to the impaired in vivo engraftment of hPSC-derived hematopoietic cells, the identification of SOX17 as a key regulator linking arterial and HOXA programs in HE may help to program HSC fate from hPSCs. [Display omitted] •SOX17 is required for specification of DLL4+CXCR4+ arterial hemogenic endothelium (HE)•DLL4+CXCR4+ arterial HE possesses robust lympho-myeloid potential•Along with induction of arterial program, SOX17 activates HOXA gene expression in HE•SOX17 effects in HE are mediated through activation of CDX2 and NOTCH signaling Jung et al. report that SOX17 is a critical upstream factor that is required for the activation and linkage of HOXA and arterial programs in the hemogenic endothelium and for establishing DLL4+CXCR4+ arterial hemogenic endothelium with definitive lympho-myeloid potential. These SOX17 effects are mediated through the activation of CDX2 and NOTCH signaling.