author_facet Peters, Rowayda
Leyvraz, Serge
Faes‐van't Hull, Eveline
Jaunin, Philippe
Gerber, Stefan
Rollini, Pierre
Peters, Rowayda
Leyvraz, Serge
Faes‐van't Hull, Eveline
Jaunin, Philippe
Gerber, Stefan
Rollini, Pierre
author Peters, Rowayda
Leyvraz, Serge
Faes‐van't Hull, Eveline
Jaunin, Philippe
Gerber, Stefan
Rollini, Pierre
spellingShingle Peters, Rowayda
Leyvraz, Serge
Faes‐van't Hull, Eveline
Jaunin, Philippe
Gerber, Stefan
Rollini, Pierre
British Journal of Haematology
Long‐term ex vivo expansion of human fetal liver primitive haematopoietic progenitor cells in stroma‐free cultures
Hematology
author_sort peters, rowayda
spelling Peters, Rowayda Leyvraz, Serge Faes‐van't Hull, Eveline Jaunin, Philippe Gerber, Stefan Rollini, Pierre 0007-1048 1365-2141 Wiley Hematology http://dx.doi.org/10.1046/j.1365-2141.2002.03873.x <jats:p><jats:bold>Summary.</jats:bold> Successful expansion of haematopoietic cells in <jats:italic>ex vivo</jats:italic> cultures will have important applications in transplantation, gene therapy, immunotherapy and potentially also in the production of non‐haematopoietic cell types. Haematopoietic stem cells (HSC), with their capacity to both self‐renew and differentiate into all blood lineages, represent the ideal target for expansion protocols. However, human HSC are rare, poorly characterized phenotypically and genotypically, and difficult to test functionally. Defining optimal culture parameters for <jats:italic>ex vivo</jats:italic> expansion has been a major challenge. We devised a simple and reproducible stroma‐free liquid culture system enabling long‐term expansion of putative haematopoietic progenitors contained within frozen human fetal liver (FL) crude cell suspensions. Starting from a small number of total nucleated cells, a massive haematopoietic cell expansion, reaching &gt; 10<jats:sup>13</jats:sup>‐fold the input cell number after ∼300 d of culture, was consistently achieved. Cells with a primitive phenotype were present throughout the culture and also underwent a continuous expansion. Moreover, the capacity for multilineage lymphomyeloid differentiation, as well as the recloning capacity of primitive myeloid progenitors, was maintained in culture. With its better proliferative potential as compared with adult sources, FL represents a promising alternative source of HSC and the culture system described here should be useful for clinical applications.</jats:p> Long‐term <i>ex vivo</i> expansion of human fetal liver primitive haematopoietic progenitor cells in stroma‐free cultures British Journal of Haematology
doi_str_mv 10.1046/j.1365-2141.2002.03873.x
facet_avail Online
Free
finc_class_facet Medizin
format ElectronicArticle
fullrecord blob:ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTA0Ni9qLjEzNjUtMjE0MS4yMDAyLjAzODczLng
id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTA0Ni9qLjEzNjUtMjE0MS4yMDAyLjAzODczLng
institution DE-Gla1
DE-Zi4
DE-15
DE-Pl11
DE-Rs1
DE-105
DE-14
DE-Ch1
DE-L229
DE-D275
DE-Bn3
DE-Brt1
DE-Zwi2
DE-D161
imprint Wiley, 2002
imprint_str_mv Wiley, 2002
issn 1365-2141
0007-1048
issn_str_mv 1365-2141
0007-1048
language English
mega_collection Wiley (CrossRef)
match_str peters2002longtermexvivoexpansionofhumanfetalliverprimitivehaematopoieticprogenitorcellsinstromafreecultures
publishDateSort 2002
publisher Wiley
recordtype ai
record_format ai
series British Journal of Haematology
source_id 49
title Long‐term ex vivo expansion of human fetal liver primitive haematopoietic progenitor cells in stroma‐free cultures
title_unstemmed Long‐term ex vivo expansion of human fetal liver primitive haematopoietic progenitor cells in stroma‐free cultures
title_full Long‐term ex vivo expansion of human fetal liver primitive haematopoietic progenitor cells in stroma‐free cultures
title_fullStr Long‐term ex vivo expansion of human fetal liver primitive haematopoietic progenitor cells in stroma‐free cultures
title_full_unstemmed Long‐term ex vivo expansion of human fetal liver primitive haematopoietic progenitor cells in stroma‐free cultures
title_short Long‐term ex vivo expansion of human fetal liver primitive haematopoietic progenitor cells in stroma‐free cultures
title_sort long‐term <i>ex vivo</i> expansion of human fetal liver primitive haematopoietic progenitor cells in stroma‐free cultures
topic Hematology
url http://dx.doi.org/10.1046/j.1365-2141.2002.03873.x
publishDate 2002
physical 792-802
description <jats:p><jats:bold>Summary.</jats:bold> Successful expansion of haematopoietic cells in <jats:italic>ex vivo</jats:italic> cultures will have important applications in transplantation, gene therapy, immunotherapy and potentially also in the production of non‐haematopoietic cell types. Haematopoietic stem cells (HSC), with their capacity to both self‐renew and differentiate into all blood lineages, represent the ideal target for expansion protocols. However, human HSC are rare, poorly characterized phenotypically and genotypically, and difficult to test functionally. Defining optimal culture parameters for <jats:italic>ex vivo</jats:italic> expansion has been a major challenge. We devised a simple and reproducible stroma‐free liquid culture system enabling long‐term expansion of putative haematopoietic progenitors contained within frozen human fetal liver (FL) crude cell suspensions. Starting from a small number of total nucleated cells, a massive haematopoietic cell expansion, reaching &gt; 10<jats:sup>13</jats:sup>‐fold the input cell number after ∼300 d of culture, was consistently achieved. Cells with a primitive phenotype were present throughout the culture and also underwent a continuous expansion. Moreover, the capacity for multilineage lymphomyeloid differentiation, as well as the recloning capacity of primitive myeloid progenitors, was maintained in culture. With its better proliferative potential as compared with adult sources, FL represents a promising alternative source of HSC and the culture system described here should be useful for clinical applications.</jats:p>
container_issue 3
container_start_page 792
container_title British Journal of Haematology
container_volume 119
format_de105 Article, E-Article
format_de14 Article, E-Article
format_de15 Article, E-Article
format_de520 Article, E-Article
format_de540 Article, E-Article
format_dech1 Article, E-Article
format_ded117 Article, E-Article
format_degla1 E-Article
format_del152 Buch
format_del189 Article, E-Article
format_dezi4 Article
format_dezwi2 Article, E-Article
format_finc Article, E-Article
format_nrw Article, E-Article
_version_ 1792336127178309634
geogr_code not assigned
last_indexed 2024-03-01T14:55:13.432Z
geogr_code_person not assigned
openURL url_ver=Z39.88-2004&ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fvufind.svn.sourceforge.net%3Agenerator&rft.title=Long%E2%80%90term+ex+vivo+expansion+of+human+fetal+liver+primitive+haematopoietic+progenitor+cells+in+stroma%E2%80%90free+cultures&rft.date=2002-12-01&genre=article&issn=1365-2141&volume=119&issue=3&spage=792&epage=802&pages=792-802&jtitle=British+Journal+of+Haematology&atitle=Long%E2%80%90term+%3Ci%3Eex+vivo%3C%2Fi%3E+expansion+of+human+fetal+liver+primitive+haematopoietic+progenitor+cells+in+stroma%E2%80%90free+cultures&aulast=Rollini&aufirst=Pierre&rft_id=info%3Adoi%2F10.1046%2Fj.1365-2141.2002.03873.x&rft.language%5B0%5D=eng
SOLR
_version_ 1792336127178309634
author Peters, Rowayda, Leyvraz, Serge, Faes‐van't Hull, Eveline, Jaunin, Philippe, Gerber, Stefan, Rollini, Pierre
author_facet Peters, Rowayda, Leyvraz, Serge, Faes‐van't Hull, Eveline, Jaunin, Philippe, Gerber, Stefan, Rollini, Pierre, Peters, Rowayda, Leyvraz, Serge, Faes‐van't Hull, Eveline, Jaunin, Philippe, Gerber, Stefan, Rollini, Pierre
author_sort peters, rowayda
container_issue 3
container_start_page 792
container_title British Journal of Haematology
container_volume 119
description <jats:p><jats:bold>Summary.</jats:bold> Successful expansion of haematopoietic cells in <jats:italic>ex vivo</jats:italic> cultures will have important applications in transplantation, gene therapy, immunotherapy and potentially also in the production of non‐haematopoietic cell types. Haematopoietic stem cells (HSC), with their capacity to both self‐renew and differentiate into all blood lineages, represent the ideal target for expansion protocols. However, human HSC are rare, poorly characterized phenotypically and genotypically, and difficult to test functionally. Defining optimal culture parameters for <jats:italic>ex vivo</jats:italic> expansion has been a major challenge. We devised a simple and reproducible stroma‐free liquid culture system enabling long‐term expansion of putative haematopoietic progenitors contained within frozen human fetal liver (FL) crude cell suspensions. Starting from a small number of total nucleated cells, a massive haematopoietic cell expansion, reaching &gt; 10<jats:sup>13</jats:sup>‐fold the input cell number after ∼300 d of culture, was consistently achieved. Cells with a primitive phenotype were present throughout the culture and also underwent a continuous expansion. Moreover, the capacity for multilineage lymphomyeloid differentiation, as well as the recloning capacity of primitive myeloid progenitors, was maintained in culture. With its better proliferative potential as compared with adult sources, FL represents a promising alternative source of HSC and the culture system described here should be useful for clinical applications.</jats:p>
doi_str_mv 10.1046/j.1365-2141.2002.03873.x
facet_avail Online, Free
finc_class_facet Medizin
format ElectronicArticle
format_de105 Article, E-Article
format_de14 Article, E-Article
format_de15 Article, E-Article
format_de520 Article, E-Article
format_de540 Article, E-Article
format_dech1 Article, E-Article
format_ded117 Article, E-Article
format_degla1 E-Article
format_del152 Buch
format_del189 Article, E-Article
format_dezi4 Article
format_dezwi2 Article, E-Article
format_finc Article, E-Article
format_nrw Article, E-Article
geogr_code not assigned
geogr_code_person not assigned
id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTA0Ni9qLjEzNjUtMjE0MS4yMDAyLjAzODczLng
imprint Wiley, 2002
imprint_str_mv Wiley, 2002
institution DE-Gla1, DE-Zi4, DE-15, DE-Pl11, DE-Rs1, DE-105, DE-14, DE-Ch1, DE-L229, DE-D275, DE-Bn3, DE-Brt1, DE-Zwi2, DE-D161
issn 1365-2141, 0007-1048
issn_str_mv 1365-2141, 0007-1048
language English
last_indexed 2024-03-01T14:55:13.432Z
match_str peters2002longtermexvivoexpansionofhumanfetalliverprimitivehaematopoieticprogenitorcellsinstromafreecultures
mega_collection Wiley (CrossRef)
physical 792-802
publishDate 2002
publishDateSort 2002
publisher Wiley
record_format ai
recordtype ai
series British Journal of Haematology
source_id 49
spelling Peters, Rowayda Leyvraz, Serge Faes‐van't Hull, Eveline Jaunin, Philippe Gerber, Stefan Rollini, Pierre 0007-1048 1365-2141 Wiley Hematology http://dx.doi.org/10.1046/j.1365-2141.2002.03873.x <jats:p><jats:bold>Summary.</jats:bold> Successful expansion of haematopoietic cells in <jats:italic>ex vivo</jats:italic> cultures will have important applications in transplantation, gene therapy, immunotherapy and potentially also in the production of non‐haematopoietic cell types. Haematopoietic stem cells (HSC), with their capacity to both self‐renew and differentiate into all blood lineages, represent the ideal target for expansion protocols. However, human HSC are rare, poorly characterized phenotypically and genotypically, and difficult to test functionally. Defining optimal culture parameters for <jats:italic>ex vivo</jats:italic> expansion has been a major challenge. We devised a simple and reproducible stroma‐free liquid culture system enabling long‐term expansion of putative haematopoietic progenitors contained within frozen human fetal liver (FL) crude cell suspensions. Starting from a small number of total nucleated cells, a massive haematopoietic cell expansion, reaching &gt; 10<jats:sup>13</jats:sup>‐fold the input cell number after ∼300 d of culture, was consistently achieved. Cells with a primitive phenotype were present throughout the culture and also underwent a continuous expansion. Moreover, the capacity for multilineage lymphomyeloid differentiation, as well as the recloning capacity of primitive myeloid progenitors, was maintained in culture. With its better proliferative potential as compared with adult sources, FL represents a promising alternative source of HSC and the culture system described here should be useful for clinical applications.</jats:p> Long‐term <i>ex vivo</i> expansion of human fetal liver primitive haematopoietic progenitor cells in stroma‐free cultures British Journal of Haematology
spellingShingle Peters, Rowayda, Leyvraz, Serge, Faes‐van't Hull, Eveline, Jaunin, Philippe, Gerber, Stefan, Rollini, Pierre, British Journal of Haematology, Long‐term ex vivo expansion of human fetal liver primitive haematopoietic progenitor cells in stroma‐free cultures, Hematology
title Long‐term ex vivo expansion of human fetal liver primitive haematopoietic progenitor cells in stroma‐free cultures
title_full Long‐term ex vivo expansion of human fetal liver primitive haematopoietic progenitor cells in stroma‐free cultures
title_fullStr Long‐term ex vivo expansion of human fetal liver primitive haematopoietic progenitor cells in stroma‐free cultures
title_full_unstemmed Long‐term ex vivo expansion of human fetal liver primitive haematopoietic progenitor cells in stroma‐free cultures
title_short Long‐term ex vivo expansion of human fetal liver primitive haematopoietic progenitor cells in stroma‐free cultures
title_sort long‐term <i>ex vivo</i> expansion of human fetal liver primitive haematopoietic progenitor cells in stroma‐free cultures
title_unstemmed Long‐term ex vivo expansion of human fetal liver primitive haematopoietic progenitor cells in stroma‐free cultures
topic Hematology
url http://dx.doi.org/10.1046/j.1365-2141.2002.03873.x