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Global microRNA profiling uncovers miR-206 as a negative regulator of hematopoietic commitment in human pluripotent stem cells

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Flamant, S. | Chomel, J.-C. | Desterke, C. | Féraud, O. | Gobbo, E. | Mitjavila-Garcia, M.-T. | Foudi, A. | Griscelli, F. | Turhan, A.G. | Bennaceur-Griscelli, A.

Edité par CCSD ; MDPI -

International audience. Although human pluripotent stem cells (hPSCs) can theoretically differentiate into any cell type, their ability to produce hematopoietic cells is highly variable from one cell line to another. The underlying mechanisms of this heterogeneity are not clearly understood. Here, using a whole miRNome analysis approach in hPSCs, we discovered that their hematopoietic competency was associated with the expression of several miRNAs and conversely correlated to that of miR-206 specifically. Lentiviral-based miR-206 ectopic expression in H1 hematopoietic competent embryonic stem (ES) cells markedly impaired their differentiation toward the blood lineage. Integrative bioinformatics identified a potential miR-206 target gene network which included hematopoietic master regulators RUNX1 and TAL1. This work sheds light on the critical role of miR-206 in the generation of blood cells off hPSCs. Our results pave the way for future genetic manipulation of hPSCs aimed at increasing their blood regenerative potential and designing better protocols for the generation of bona fide hPSC-derived hematopoietic stem cells. © 2019 by the authors. Licensee MDPI, Basel, Switzerland.

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