Microporous Membrane-based Co-culture of Human Embryonic Stem Cells

Transwell inserts with microporous membranes, available from multiple commercial sources, have been widely used for various mammalian cell culture applications, including the reduction of cell culture mixing. In this study, we examined the feasibility and functionality of using this technology for s...

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Main Author: Albert, Kelsey Morgan
Format: Others
Published: VCU Scholars Compass 2007
Subjects:
HFF
Online Access:http://scholarscompass.vcu.edu/etd_retro/161
http://scholarscompass.vcu.edu/cgi/viewcontent.cgi?article=1160&context=etd_retro
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spelling ndltd-vcu.edu-oai-scholarscompass.vcu.edu-etd_retro-11602017-03-17T08:25:39Z Microporous Membrane-based Co-culture of Human Embryonic Stem Cells Albert, Kelsey Morgan Transwell inserts with microporous membranes, available from multiple commercial sources, have been widely used for various mammalian cell culture applications, including the reduction of cell culture mixing. In this study, we examined the feasibility and functionality of using this technology for separating human embryonic stem cells (hESCs) from their respective feeder cells. We found that when hESCs were propagated on transwell inserts positioned directly above feeder cells grown in a separate dish, the hESCs could be maintained in an undifferentiated state for over 10 passages with no change in their basic pluripotent characteristics. In parallel with our transwell insert experiments, we also evaluated the ability of a new defined, xeno-free medium, HEScGRO™, to enhance the animal-free characteristics of the transwell insert-based culture system. Results from our studies demonstrate that HEScGRO™ medium assists in maintaining the pluripotent characteristics of hESCs propagated in the transwell insert- based culture system. These combined results represent a significant development in properly segregating stem cells from their feeders, thus eliminating cell mixing, contamination, and providing the cells with a superior environment for nourishment and controlled self-renewal. Overall, this development in hESC propagation could have wide-reaching applications for self-renewal and differentiation studies within the field of stem cell biology. 2007-01-01T08:00:00Z text application/pdf http://scholarscompass.vcu.edu/etd_retro/161 http://scholarscompass.vcu.edu/cgi/viewcontent.cgi?article=1160&context=etd_retro © The Author Retrospective ETD Collection VCU Scholars Compass transwell insert filter mesh barricade microporous hESC stem cells human embryonic stem cells membrane HFF co-culture Biology Life Sciences
collection NDLTD
format Others
sources NDLTD
topic transwell
insert
filter
mesh barricade
microporous
hESC
stem cells
human embryonic stem cells
membrane
HFF
co-culture
Biology
Life Sciences
spellingShingle transwell
insert
filter
mesh barricade
microporous
hESC
stem cells
human embryonic stem cells
membrane
HFF
co-culture
Biology
Life Sciences
Albert, Kelsey Morgan
Microporous Membrane-based Co-culture of Human Embryonic Stem Cells
description Transwell inserts with microporous membranes, available from multiple commercial sources, have been widely used for various mammalian cell culture applications, including the reduction of cell culture mixing. In this study, we examined the feasibility and functionality of using this technology for separating human embryonic stem cells (hESCs) from their respective feeder cells. We found that when hESCs were propagated on transwell inserts positioned directly above feeder cells grown in a separate dish, the hESCs could be maintained in an undifferentiated state for over 10 passages with no change in their basic pluripotent characteristics. In parallel with our transwell insert experiments, we also evaluated the ability of a new defined, xeno-free medium, HEScGRO™, to enhance the animal-free characteristics of the transwell insert-based culture system. Results from our studies demonstrate that HEScGRO™ medium assists in maintaining the pluripotent characteristics of hESCs propagated in the transwell insert- based culture system. These combined results represent a significant development in properly segregating stem cells from their feeders, thus eliminating cell mixing, contamination, and providing the cells with a superior environment for nourishment and controlled self-renewal. Overall, this development in hESC propagation could have wide-reaching applications for self-renewal and differentiation studies within the field of stem cell biology.
author Albert, Kelsey Morgan
author_facet Albert, Kelsey Morgan
author_sort Albert, Kelsey Morgan
title Microporous Membrane-based Co-culture of Human Embryonic Stem Cells
title_short Microporous Membrane-based Co-culture of Human Embryonic Stem Cells
title_full Microporous Membrane-based Co-culture of Human Embryonic Stem Cells
title_fullStr Microporous Membrane-based Co-culture of Human Embryonic Stem Cells
title_full_unstemmed Microporous Membrane-based Co-culture of Human Embryonic Stem Cells
title_sort microporous membrane-based co-culture of human embryonic stem cells
publisher VCU Scholars Compass
publishDate 2007
url http://scholarscompass.vcu.edu/etd_retro/161
http://scholarscompass.vcu.edu/cgi/viewcontent.cgi?article=1160&context=etd_retro
work_keys_str_mv AT albertkelseymorgan microporousmembranebasedcocultureofhumanembryonicstemcells
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