LIF-free embryonic stem cell culture in simulated microgravity.
<h4>Background</h4>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 cli...
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2009
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oai:doaj.org-article:9a3c9e03e57448ccaafe52842fa62eb82021-11-25T06:21:27ZLIF-free embryonic stem cell culture in simulated microgravity.1932-620310.1371/journal.pone.0006343https://doaj.org/article/9a3c9e03e57448ccaafe52842fa62eb82009-07-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/19626124/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>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.<h4>Methodology/principal findings</h4>We cultured mouse ES cells in simulated microgravity using a 3D-clinostat. We used feeder-free and serum-free media without LIF.<h4>Conclusions/significance</h4>Here we show that simulated microgravity allows novel LIF-free and animal derived material-free culture methods for mouse ES cells.Yumi KawaharaTomotaka ManabeMasaya MatsumotoTeruyuki KajiumeMasayasu MatsumotoLouis YugePublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 4, Iss 7, p e6343 (2009) |
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Medicine R Science Q Yumi Kawahara Tomotaka Manabe Masaya Matsumoto Teruyuki Kajiume Masayasu Matsumoto Louis Yuge LIF-free embryonic stem cell culture in simulated microgravity. |
description |
<h4>Background</h4>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.<h4>Methodology/principal findings</h4>We cultured mouse ES cells in simulated microgravity using a 3D-clinostat. We used feeder-free and serum-free media without LIF.<h4>Conclusions/significance</h4>Here we show that simulated microgravity allows novel LIF-free and animal derived material-free culture methods for mouse ES cells. |
format |
article |
author |
Yumi Kawahara Tomotaka Manabe Masaya Matsumoto Teruyuki Kajiume Masayasu Matsumoto Louis Yuge |
author_facet |
Yumi Kawahara Tomotaka Manabe Masaya Matsumoto Teruyuki Kajiume Masayasu Matsumoto Louis Yuge |
author_sort |
Yumi Kawahara |
title |
LIF-free embryonic stem cell culture in simulated microgravity. |
title_short |
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_sort |
lif-free embryonic stem cell culture in simulated microgravity. |
publisher |
Public Library of Science (PLoS) |
publishDate |
2009 |
url |
https://doaj.org/article/9a3c9e03e57448ccaafe52842fa62eb8 |
work_keys_str_mv |
AT yumikawahara liffreeembryonicstemcellcultureinsimulatedmicrogravity AT tomotakamanabe liffreeembryonicstemcellcultureinsimulatedmicrogravity AT masayamatsumoto liffreeembryonicstemcellcultureinsimulatedmicrogravity AT teruyukikajiume liffreeembryonicstemcellcultureinsimulatedmicrogravity AT masayasumatsumoto liffreeembryonicstemcellcultureinsimulatedmicrogravity AT louisyuge liffreeembryonicstemcellcultureinsimulatedmicrogravity |
_version_ |
1718413815437066240 |