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Book Chapter: Derivation of hematopoietic stem and progenitor cells from human pluripotent stem cells

TitleDerivation of hematopoietic stem and progenitor cells from human pluripotent stem cells
Authors
KeywordsPluripotent stem cells
Gene regulatory network
Hematopoietic stem cells
Issue Date2019
PublisherHumana.
Citation
Derivation of Hematopoietic Stem and Progenitor Cells from Human Pluripotent Stem Cells. In Hyun, I, De Los Angeles, A (Eds.), Chimera Research: Methods and Protocols, p. 37-41. New York, NY: Humana, 2019 How to Cite?
AbstractHematopoietic stem cell (HSC) transplantation is a curative treatment for hematologic malignancies and innate immunodeficiency, but its applications are limited to matched donors, and the availability of umbilical cord blood of immune types. Therefore, derivation of HSCs from patient-specific human induced pluripotent stem cells (hiPSCs) is a holy grail in regenerative medicine. However, derivation of HSCs from iPSCs has proven elusive. Here, the authors developed a method to derive hematopoietic stem and progenitor cells (HSPCs) by combining two established methods. The first method mimics embryonic development by directed differentiation of iPSCs into a cellular state termed hemogenic endothelium (HE) by stepwise exposure to different combinations of morphogens and cytokines. In the second method, transcription factors are induced in HE cells for specification into HSCs. By combining these approaches, the authors identified a set of select transcription factors that programmed HE cells into HSPCs with long-term and multilineage capacity in vivo. In this chapter, I provide an overview of this technology, technical tips, and future applications.
Persistent Identifierhttp://hdl.handle.net/10722/295413
ISSN
2023 SCImago Journal Rankings: 0.399
Series/Report no.Methods in Molecular Biology ; 2005

 

DC FieldValueLanguage
dc.contributor.authorSugimura, Ryohichi-
dc.date.accessioned2021-01-18T15:46:49Z-
dc.date.available2021-01-18T15:46:49Z-
dc.date.issued2019-
dc.identifier.citationDerivation of Hematopoietic Stem and Progenitor Cells from Human Pluripotent Stem Cells. In Hyun, I, De Los Angeles, A (Eds.), Chimera Research: Methods and Protocols, p. 37-41. New York, NY: Humana, 2019-
dc.identifier.issn1064-3745-
dc.identifier.urihttp://hdl.handle.net/10722/295413-
dc.description.abstractHematopoietic stem cell (HSC) transplantation is a curative treatment for hematologic malignancies and innate immunodeficiency, but its applications are limited to matched donors, and the availability of umbilical cord blood of immune types. Therefore, derivation of HSCs from patient-specific human induced pluripotent stem cells (hiPSCs) is a holy grail in regenerative medicine. However, derivation of HSCs from iPSCs has proven elusive. Here, the authors developed a method to derive hematopoietic stem and progenitor cells (HSPCs) by combining two established methods. The first method mimics embryonic development by directed differentiation of iPSCs into a cellular state termed hemogenic endothelium (HE) by stepwise exposure to different combinations of morphogens and cytokines. In the second method, transcription factors are induced in HE cells for specification into HSCs. By combining these approaches, the authors identified a set of select transcription factors that programmed HE cells into HSPCs with long-term and multilineage capacity in vivo. In this chapter, I provide an overview of this technology, technical tips, and future applications.-
dc.languageeng-
dc.publisherHumana.-
dc.relation.ispartofChimera Research: Methods and Protocols-
dc.relation.ispartofseriesMethods in Molecular Biology ; 2005-
dc.subjectPluripotent stem cells-
dc.subjectGene regulatory network-
dc.subjectHematopoietic stem cells-
dc.titleDerivation of hematopoietic stem and progenitor cells from human pluripotent stem cells-
dc.typeBook_Chapter-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1007/978-1-4939-9524-0_3-
dc.identifier.pmid31175644-
dc.identifier.scopuseid_2-s2.0-85066985459-
dc.identifier.spage37-
dc.identifier.epage41-
dc.identifier.eissn1940-6029-
dc.publisher.placeNew York, NY-
dc.identifier.issnl1064-3745-

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