Cargando…

Hematopoietic stem cells derive directly from aortic endothelium during development

A major goal of regenerative medicine is to instruct formation of multipotent, tissue-specific stem cells from induced pluripotent stem cells (iPSCs) for cell replacement therapies. Generation of hematopoietic stem cells (HSCs) from iPSCs or embryonic stem cells (ESCs) is not currently possible, how...

Descripción completa

Detalles Bibliográficos
Autores principales: Bertrand, Julien Y., Chi, Neil C., Santoso, Buyung, Teng, Shutian, Stainier, Didier Y. R., Traver, David
Formato: Texto
Lenguaje:English
Publicado: 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2858358/
https://www.ncbi.nlm.nih.gov/pubmed/20154733
http://dx.doi.org/10.1038/nature08738
_version_ 1782180415497306112
author Bertrand, Julien Y.
Chi, Neil C.
Santoso, Buyung
Teng, Shutian
Stainier, Didier Y. R.
Traver, David
author_facet Bertrand, Julien Y.
Chi, Neil C.
Santoso, Buyung
Teng, Shutian
Stainier, Didier Y. R.
Traver, David
author_sort Bertrand, Julien Y.
collection PubMed
description A major goal of regenerative medicine is to instruct formation of multipotent, tissue-specific stem cells from induced pluripotent stem cells (iPSCs) for cell replacement therapies. Generation of hematopoietic stem cells (HSCs) from iPSCs or embryonic stem cells (ESCs) is not currently possible, however, necessitating a better understanding of how HSCs normally arise during embryonic development. We previously showed that hematopoiesis occurs through four distinct waves during zebrafish development, with HSCs arising in the final wave in close association with the dorsal aorta. Recent reports have suggested that murine HSCs derive from hemogenic endothelial cells (ECs) lining the aortic floor1,2. Additional in vitro studies have similarly suggested that the hematopoietic progeny of ESCs arise through intermediates with endothelial potential3,4. In this report, we have utilized the unique strengths of the zebrafish embryo to image directly the birth of HSCs from the ventral wall of the dorsal aorta. Utilizing combinations of fluorescent reporter transgenes, confocal timelapse microscopy and flow cytometry, we have identified and isolated the stepwise intermediates as aortic hemogenic endothelium transitions to nascent HSCs. Finally, using a permanent lineage tracing strategy, we demonstrate that the HSCs generated from hemogenic endothelium are the lineal founders of the adult hematopoietic system.
format Text
id pubmed-2858358
institution National Center for Biotechnology Information
language English
publishDate 2010
record_format MEDLINE/PubMed
spelling pubmed-28583582010-09-04 Hematopoietic stem cells derive directly from aortic endothelium during development Bertrand, Julien Y. Chi, Neil C. Santoso, Buyung Teng, Shutian Stainier, Didier Y. R. Traver, David Nature Article A major goal of regenerative medicine is to instruct formation of multipotent, tissue-specific stem cells from induced pluripotent stem cells (iPSCs) for cell replacement therapies. Generation of hematopoietic stem cells (HSCs) from iPSCs or embryonic stem cells (ESCs) is not currently possible, however, necessitating a better understanding of how HSCs normally arise during embryonic development. We previously showed that hematopoiesis occurs through four distinct waves during zebrafish development, with HSCs arising in the final wave in close association with the dorsal aorta. Recent reports have suggested that murine HSCs derive from hemogenic endothelial cells (ECs) lining the aortic floor1,2. Additional in vitro studies have similarly suggested that the hematopoietic progeny of ESCs arise through intermediates with endothelial potential3,4. In this report, we have utilized the unique strengths of the zebrafish embryo to image directly the birth of HSCs from the ventral wall of the dorsal aorta. Utilizing combinations of fluorescent reporter transgenes, confocal timelapse microscopy and flow cytometry, we have identified and isolated the stepwise intermediates as aortic hemogenic endothelium transitions to nascent HSCs. Finally, using a permanent lineage tracing strategy, we demonstrate that the HSCs generated from hemogenic endothelium are the lineal founders of the adult hematopoietic system. 2010-02-14 2010-03-04 /pmc/articles/PMC2858358/ /pubmed/20154733 http://dx.doi.org/10.1038/nature08738 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Bertrand, Julien Y.
Chi, Neil C.
Santoso, Buyung
Teng, Shutian
Stainier, Didier Y. R.
Traver, David
Hematopoietic stem cells derive directly from aortic endothelium during development
title Hematopoietic stem cells derive directly from aortic endothelium during development
title_full Hematopoietic stem cells derive directly from aortic endothelium during development
title_fullStr Hematopoietic stem cells derive directly from aortic endothelium during development
title_full_unstemmed Hematopoietic stem cells derive directly from aortic endothelium during development
title_short Hematopoietic stem cells derive directly from aortic endothelium during development
title_sort hematopoietic stem cells derive directly from aortic endothelium during development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2858358/
https://www.ncbi.nlm.nih.gov/pubmed/20154733
http://dx.doi.org/10.1038/nature08738
work_keys_str_mv AT bertrandjulieny hematopoieticstemcellsderivedirectlyfromaorticendotheliumduringdevelopment
AT chineilc hematopoieticstemcellsderivedirectlyfromaorticendotheliumduringdevelopment
AT santosobuyung hematopoieticstemcellsderivedirectlyfromaorticendotheliumduringdevelopment
AT tengshutian hematopoieticstemcellsderivedirectlyfromaorticendotheliumduringdevelopment
AT stainierdidieryr hematopoieticstemcellsderivedirectlyfromaorticendotheliumduringdevelopment
AT traverdavid hematopoieticstemcellsderivedirectlyfromaorticendotheliumduringdevelopment