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Direct Induction of Hematoendothelial Programs in Human Pluripotent Stem Cells by Transcriptional Regulators

Advancing pluripotent stem cell technologies for modeling hematopoietic stem cell development and blood therapies requires identifying key regulators of hematopoietic commitment from human pluripotent stem cells (hPSCs). Here, by screening the effect of 27 candidate factors, we reveal two groups of...

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Detalles Bibliográficos
Autores principales: Elcheva, Irina, Brok-Volchanskaya, Vera, Kumar, Akhilesh, Liu, Patricia, Lee, Jeong-Hee, Tong, Lilian, Vodyanik, Maxim, Swanson, Scott, Stewart, Ron, Kyba, Michael, Yakubov, Eduard, Cooke, John, Thomson, James A., Slukvin, Igor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4107340/
https://www.ncbi.nlm.nih.gov/pubmed/25019369
http://dx.doi.org/10.1038/ncomms5372
Descripción
Sumario:Advancing pluripotent stem cell technologies for modeling hematopoietic stem cell development and blood therapies requires identifying key regulators of hematopoietic commitment from human pluripotent stem cells (hPSCs). Here, by screening the effect of 27 candidate factors, we reveal two groups of transcriptional regulators capable of inducing distinct hematopoietic programs from hPSCs: panmyeloid (ETV2 and GATA2) and erythro-megakaryocytic (GATA2 and TAL1). In both cases, these transcription factors directly convert hPSCs to endothelium, which subsequently transforms into blood cells with pan-myeloid or erythromegakaryocytic potential. These data demonstrate that two distinct genetic programs regulate the hematopoietic development from hPSCs and that both of these programs specify hPSCs directly to hemogenic endothelial cells. Additionally, this study provides a novel method for the efficient induction of blood and endothelial cells from hPSCs via overexpression of modified mRNA for the selected transcription factors.