Show simple item record

dc.contributor.authorCosta, Guilherme
dc.contributor.authorKouskoff, Valerie
dc.contributor.authorLacaud, Georges
dc.date.accessioned2012-05-09T12:51:42Z
dc.date.available2012-05-09T12:51:42Z
dc.date.issued2012-02-23
dc.identifier.citationOrigin of blood cells and HSC production in the embryo. 2012, 33(5):215-223 Trends Immunolen_GB
dc.identifier.issn1471-4981
dc.identifier.pmid22365572
dc.identifier.doi10.1016/j.it.2012.01.012
dc.identifier.urihttp://hdl.handle.net/10541/222735
dc.description.abstractHematopoietic stem cells (HSCs) are capable of self-renewal and differentiation into all blood cell types. During adult life, they reside in the bone marrow in a quiescent state. By contrast, in the growing embryo hematopoiesis is sequentially found in several developmental niches. This review provides an overview of the still controversial contribution of each of these embryonic sites to the final pool of adult HSCs and discusses new insights into the cellular origin and the molecular regulation implicated in the generation of blood progenitor cells. A better understanding of HSC development during ontogeny is essential to develop new strategies to amplify HSCs or to generate them from embryonic stem cells or by somatic cell reprogramming.
dc.languageENG
dc.language.isoenen
dc.rightsArchived with thanks to Trends in immunologyen_GB
dc.titleOrigin of blood cells and HSC production in the embryo.en
dc.typeArticleen
dc.contributor.departmentCancer Research UK Stem Cell Hematopoiesis Group, Paterson Institute for Cancer Research, University of Manchester, Wilmslow Road, Manchester M20 4BX, UK; Graduate Program in Areas of Basic and Applied Biology (GABBA), University of Porto, Porto, Portugal.en_GB
dc.identifier.journalTrends in Immunologyen_GB
html.description.abstractHematopoietic stem cells (HSCs) are capable of self-renewal and differentiation into all blood cell types. During adult life, they reside in the bone marrow in a quiescent state. By contrast, in the growing embryo hematopoiesis is sequentially found in several developmental niches. This review provides an overview of the still controversial contribution of each of these embryonic sites to the final pool of adult HSCs and discusses new insights into the cellular origin and the molecular regulation implicated in the generation of blood progenitor cells. A better understanding of HSC development during ontogeny is essential to develop new strategies to amplify HSCs or to generate them from embryonic stem cells or by somatic cell reprogramming.


Files in this item

This item appears in the following Collection(s)

Show simple item record