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LIF-Free Embryonic Stem Cell Culture in Simulated Microgravity

BACKGROUND: Leukemia inhibitory factor (LIF) is an indispensable factor for maintaining mouse embryonic stem (ES) cell pluripotency. A feeder layer and serum are also needed to maintain an undifferentiated state, however, such animal derived materials need to be eliminated for clinical applications....

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Detalles Bibliográficos
Autores principales: Kawahara, Yumi, Manabe, Tomotaka, Matsumoto, Masaya, Kajiume, Teruyuki, Matsumoto, Masayasu, Yuge, Louis
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2710515/
https://www.ncbi.nlm.nih.gov/pubmed/19626124
http://dx.doi.org/10.1371/journal.pone.0006343
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author Kawahara, Yumi
Manabe, Tomotaka
Matsumoto, Masaya
Kajiume, Teruyuki
Matsumoto, Masayasu
Yuge, Louis
author_facet Kawahara, Yumi
Manabe, Tomotaka
Matsumoto, Masaya
Kajiume, Teruyuki
Matsumoto, Masayasu
Yuge, Louis
author_sort Kawahara, Yumi
collection PubMed
description BACKGROUND: Leukemia inhibitory factor (LIF) is an indispensable factor for maintaining mouse embryonic stem (ES) cell pluripotency. A feeder layer and serum are also needed to maintain an undifferentiated state, however, such animal derived materials need to be eliminated for clinical applications. Therefore, a more reliable ES cell culture technique is required. METHODOLOGY/PRINCIPAL FINDINGS: We cultured mouse ES cells in simulated microgravity using a 3D-clinostat. We used feeder-free and serum-free media without LIF. CONCLUSIONS/SIGNIFICANCE: Here we show that simulated microgravity allows novel LIF-free and animal derived material-free culture methods for mouse ES cells.
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spelling pubmed-27105152009-07-23 LIF-Free Embryonic Stem Cell Culture in Simulated Microgravity Kawahara, Yumi Manabe, Tomotaka Matsumoto, Masaya Kajiume, Teruyuki Matsumoto, Masayasu Yuge, Louis PLoS One Research Article BACKGROUND: Leukemia inhibitory factor (LIF) is an indispensable factor for maintaining mouse embryonic stem (ES) cell pluripotency. A feeder layer and serum are also needed to maintain an undifferentiated state, however, such animal derived materials need to be eliminated for clinical applications. Therefore, a more reliable ES cell culture technique is required. METHODOLOGY/PRINCIPAL FINDINGS: We cultured mouse ES cells in simulated microgravity using a 3D-clinostat. We used feeder-free and serum-free media without LIF. CONCLUSIONS/SIGNIFICANCE: Here we show that simulated microgravity allows novel LIF-free and animal derived material-free culture methods for mouse ES cells. Public Library of Science 2009-07-23 /pmc/articles/PMC2710515/ /pubmed/19626124 http://dx.doi.org/10.1371/journal.pone.0006343 Text en Kawahara 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.
spellingShingle Research Article
Kawahara, Yumi
Manabe, Tomotaka
Matsumoto, Masaya
Kajiume, Teruyuki
Matsumoto, Masayasu
Yuge, Louis
LIF-Free Embryonic Stem Cell Culture in Simulated Microgravity
title LIF-Free Embryonic Stem Cell Culture in Simulated Microgravity
title_full LIF-Free Embryonic Stem Cell Culture in Simulated Microgravity
title_fullStr LIF-Free Embryonic Stem Cell Culture in Simulated Microgravity
title_full_unstemmed LIF-Free Embryonic Stem Cell Culture in Simulated Microgravity
title_short LIF-Free Embryonic Stem Cell Culture in Simulated Microgravity
title_sort lif-free embryonic stem cell culture in simulated microgravity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2710515/
https://www.ncbi.nlm.nih.gov/pubmed/19626124
http://dx.doi.org/10.1371/journal.pone.0006343
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