Blood stem cell-forming haemogenic endothelium in zebrafish derives from arterial endothelium.
Florian BonkhoferRossella RispoliPhilip PinheiroMonika KrecsmarikJanina Schneider-SwalesIngrid Ho Ching TsangMarella de BruijnRui MonteiroTessa PeterkinRoger PatientPublished in: Nature communications (2019)
Haematopoietic stem cells are generated from the haemogenic endothelium (HE) located in the floor of the dorsal aorta (DA). Despite being integral to arteries, it is controversial whether HE and arterial endothelium share a common lineage. Here, we present a transgenic zebrafish runx1 reporter line to isolate HE and aortic roof endothelium (ARE)s, excluding non-aortic endothelium. Transcriptomic analysis of these populations identifies Runx1-regulated genes and shows that HE initially expresses arterial markers at similar levels to ARE. Furthermore, runx1 expression depends on prior arterial programming by the Notch ligand dll4. Runx1-/- mutants fail to downregulate arterial genes in the HE, which remains integrated within the DA, suggesting that Runx1 represses the pre-existing arterial programme in HE to allow progression towards the haematopoietic fate. These findings strongly suggest that, in zebrafish, aortic endothelium is a precursor to HE, with potential implications for pluripotent stem cell differentiation protocols for the generation of transplantable HSCs.
Keyphrases
- stem cells
- nitric oxide
- transcription factor
- aortic valve
- pulmonary artery
- left ventricular
- genome wide
- poor prognosis
- cell proliferation
- spinal cord
- aortic dissection
- randomized controlled trial
- single cell
- long non coding rna
- genome wide identification
- pulmonary arterial hypertension
- bone marrow
- climate change
- cell fate