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Optimization of ex vivo hematopoietic stem cell expansion in intermittent dynamic cultures

For the ex vivo expansion of CD34(+) cells, culture conditions were optimized using cytokine cocktails and media change methods. In addition, static, orbital-shake, and stirred cultures were compared. After cultivation, total cell expansion, immunophenotypes, clonogenic ability, and metabolite conce...

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Detalles Bibliográficos
Autores principales: Choi, Yong-Soo, Noh, Sang-Eun, Lim, Sang-Min, Kim, Dong-il
Formato: Texto
Lenguaje:English
Publicado: Springer Netherlands 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2974206/
https://www.ncbi.nlm.nih.gov/pubmed/20652621
http://dx.doi.org/10.1007/s10529-010-0355-0
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author Choi, Yong-Soo
Noh, Sang-Eun
Lim, Sang-Min
Kim, Dong-il
author_facet Choi, Yong-Soo
Noh, Sang-Eun
Lim, Sang-Min
Kim, Dong-il
author_sort Choi, Yong-Soo
collection PubMed
description For the ex vivo expansion of CD34(+) cells, culture conditions were optimized using cytokine cocktails and media change methods. In addition, static, orbital-shake, and stirred cultures were compared. After cultivation, total cell expansion, immunophenotypes, clonogenic ability, and metabolite concentration in media were analyzed. Optimized media change methods enhanced the number of total nucleated cells (TNCs) by 600-fold (from 10(4) to 6 × 10(6) cells) in static cultures. Furthermore, intermittent orbital-shake cultures gave the highest fold increase of TNCs and CD34(+)/CD38(−) cells. These results imply that proliferation of CD34(+) cells in intermittent shake cultures was more efficient than that in static cultures under optimized culture conditions.
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spelling pubmed-29742062010-11-29 Optimization of ex vivo hematopoietic stem cell expansion in intermittent dynamic cultures Choi, Yong-Soo Noh, Sang-Eun Lim, Sang-Min Kim, Dong-il Biotechnol Lett Original Research Paper For the ex vivo expansion of CD34(+) cells, culture conditions were optimized using cytokine cocktails and media change methods. In addition, static, orbital-shake, and stirred cultures were compared. After cultivation, total cell expansion, immunophenotypes, clonogenic ability, and metabolite concentration in media were analyzed. Optimized media change methods enhanced the number of total nucleated cells (TNCs) by 600-fold (from 10(4) to 6 × 10(6) cells) in static cultures. Furthermore, intermittent orbital-shake cultures gave the highest fold increase of TNCs and CD34(+)/CD38(−) cells. These results imply that proliferation of CD34(+) cells in intermittent shake cultures was more efficient than that in static cultures under optimized culture conditions. Springer Netherlands 2010-07-22 2010 /pmc/articles/PMC2974206/ /pubmed/20652621 http://dx.doi.org/10.1007/s10529-010-0355-0 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Research Paper
Choi, Yong-Soo
Noh, Sang-Eun
Lim, Sang-Min
Kim, Dong-il
Optimization of ex vivo hematopoietic stem cell expansion in intermittent dynamic cultures
title Optimization of ex vivo hematopoietic stem cell expansion in intermittent dynamic cultures
title_full Optimization of ex vivo hematopoietic stem cell expansion in intermittent dynamic cultures
title_fullStr Optimization of ex vivo hematopoietic stem cell expansion in intermittent dynamic cultures
title_full_unstemmed Optimization of ex vivo hematopoietic stem cell expansion in intermittent dynamic cultures
title_short Optimization of ex vivo hematopoietic stem cell expansion in intermittent dynamic cultures
title_sort optimization of ex vivo hematopoietic stem cell expansion in intermittent dynamic cultures
topic Original Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2974206/
https://www.ncbi.nlm.nih.gov/pubmed/20652621
http://dx.doi.org/10.1007/s10529-010-0355-0
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