Comparative Study of Hematopoietic Differentiation between Human Embryonic Stem Cell Lines
Directed differentiation of human embryonic stem cells (hESCs) into any desired cell type has been hailed as a therapeutic promise to cure many human diseases. However, substantial roadblocks still exist for in vitro differentiation of hESCs into distinct cell types, including T lymphocytes. Here we...
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2011
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pubmed-30956332011-05-19 Comparative Study of Hematopoietic Differentiation between Human Embryonic Stem Cell Lines Melichar, Heather Li, Ou Ross, Jenny Haber, Hilary Cado, Dragana Nolla, Hector Robey, Ellen A. Winoto, Astar Research Article Directed differentiation of human embryonic stem cells (hESCs) into any desired cell type has been hailed as a therapeutic promise to cure many human diseases. However, substantial roadblocks still exist for in vitro differentiation of hESCs into distinct cell types, including T lymphocytes. Here we examined the hematopoietic differentiation potential of six different hESC lines. We compare their ability to develop into CD34+ or CD34+CD45+ hematopoietic precursor populations under several differentiation conditions. Comparison of lymphoid potential of hESC derived- and fetal tissue derived-hematopoietic precursors was also made. We found diverse hematopoietic potential between hESC lines depending on the culture or passage conditions. In contrast to fetal-derived hematopoietic precursors, none of the CD34+ precursors differentiated from hESCs were able to develop further into T cells. These data underscore the difficulties in the current strategy of hESC forward differentiation and highlight distinct differences between CD34+ hematopoietic precursors generated in vitro versus in vivo. Public Library of Science 2011-05-16 /pmc/articles/PMC3095633/ /pubmed/21603627 http://dx.doi.org/10.1371/journal.pone.0019854 Text en Melichar et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
repository_type |
Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
building |
NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Melichar, Heather Li, Ou Ross, Jenny Haber, Hilary Cado, Dragana Nolla, Hector Robey, Ellen A. Winoto, Astar |
spellingShingle |
Melichar, Heather Li, Ou Ross, Jenny Haber, Hilary Cado, Dragana Nolla, Hector Robey, Ellen A. Winoto, Astar Comparative Study of Hematopoietic Differentiation between Human Embryonic Stem Cell Lines |
author_facet |
Melichar, Heather Li, Ou Ross, Jenny Haber, Hilary Cado, Dragana Nolla, Hector Robey, Ellen A. Winoto, Astar |
author_sort |
Melichar, Heather |
title |
Comparative Study of Hematopoietic Differentiation between Human Embryonic Stem Cell Lines |
title_short |
Comparative Study of Hematopoietic Differentiation between Human Embryonic Stem Cell Lines |
title_full |
Comparative Study of Hematopoietic Differentiation between Human Embryonic Stem Cell Lines |
title_fullStr |
Comparative Study of Hematopoietic Differentiation between Human Embryonic Stem Cell Lines |
title_full_unstemmed |
Comparative Study of Hematopoietic Differentiation between Human Embryonic Stem Cell Lines |
title_sort |
comparative study of hematopoietic differentiation between human embryonic stem cell lines |
description |
Directed differentiation of human embryonic stem cells (hESCs) into any desired cell type has been hailed as a therapeutic promise to cure many human diseases. However, substantial roadblocks still exist for in vitro differentiation of hESCs into distinct cell types, including T lymphocytes. Here we examined the hematopoietic differentiation potential of six different hESC lines. We compare their ability to develop into CD34+ or CD34+CD45+ hematopoietic precursor populations under several differentiation conditions. Comparison of lymphoid potential of hESC derived- and fetal tissue derived-hematopoietic precursors was also made. We found diverse hematopoietic potential between hESC lines depending on the culture or passage conditions. In contrast to fetal-derived hematopoietic precursors, none of the CD34+ precursors differentiated from hESCs were able to develop further into T cells. These data underscore the difficulties in the current strategy of hESC forward differentiation and highlight distinct differences between CD34+ hematopoietic precursors generated in vitro versus in vivo. |
publisher |
Public Library of Science |
publishDate |
2011 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3095633/ |
_version_ |
1611454061278658560 |