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Hydrogels as artificial matrices for human embryonic stem cell self-renewal

Human embryonic stem cells (hESCs) have the potential to differentiate into all cell types in the body and hold great promise for regenerative medicine; however, large‐scale expansion of undifferentiated hESCs remains a major challenge. Self‐renewal of hESCs requires culturing these cells on either...

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Published in:Journal of biomedical materials research 2006-10, Vol.79A (1), p.1-5
Main Authors: Li, Ying J., Chung, Eugene H., Rodriguez, Ryan T., Firpo, Meri T., Healy, Kevin E.
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Language:English
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cited_by cdi_FETCH-LOGICAL-c4952-9ed460f47637935100c8a4f785c7f5c83870cbe7158d5be25936c1d434552d5e3
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creator Li, Ying J.
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description Human embryonic stem cells (hESCs) have the potential to differentiate into all cell types in the body and hold great promise for regenerative medicine; however, large‐scale expansion of undifferentiated hESCs remains a major challenge. Self‐renewal of hESCs requires culturing these cells on either mouse or human fibroblast cells (i.e., a feeder layer of cells), or on artificial extracellular matrices (ECMs) while supplementing the media with soluble growth factors. Here we report a completely synthetic ECM system composed of a semi‐interpenetrating polymer network (sIPN), a polymer hydrogel, which was designed to allow the independent manipulation of cell adhesion ligand presentation and matrix stiffness. In the short term, hESCs that were cultured on the sIPN adhered to the surface, remained viable, maintained the morphology, and expressed the markers of undifferentiated hESCs. This was the first demonstration that a completely synthetic ECM can support short‐term self‐renewal of hESCs. © 2006 Wiley Periodicals, Inc. J Biomed Mater Res, 2006
doi_str_mv 10.1002/jbm.a.30732
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subjects artificial extracellular matrices
Biocompatible Materials
Cell Line
Cells, Cultured
human embryonic stem cells
Humans
Hydrogels
interpenetrating networks
self-renewal
Stem Cells
title Hydrogels as artificial matrices for human embryonic stem cell self-renewal
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