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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 |
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creator | Li, Ying J. Chung, Eugene H. Rodriguez, Ryan T. Firpo, Meri T. Healy, Kevin E. |
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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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. 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Biomed. Mater. Res</addtitle><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</description><subject>artificial extracellular matrices</subject><subject>Biocompatible Materials</subject><subject>Cell Line</subject><subject>Cells, Cultured</subject><subject>human embryonic stem cells</subject><subject>Humans</subject><subject>Hydrogels</subject><subject>interpenetrating networks</subject><subject>self-renewal</subject><subject>Stem Cells</subject><issn>1549-3296</issn><issn>0021-9304</issn><issn>1552-4965</issn><issn>1097-4636</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqFkbtPwzAQxi0EorwmdpSJBaXY8XsEBOVVGADBZjnOBQxJA3Yr6H-PSwtsIJ10N_zu0333IbRNcJ9gXOw_l23f9imWtFhCa4TzImda8OXZzHROCy16aD3G5wQLzItV1CNCMqKVWkMXp9MqdI_QxMymCmNfe-dtk7V2HLyDmNVdyJ4mrR1l0JZh2o28y-IY2sxB02QRmjoPMIJ322yildo2EbYWfQPdnRzfHp3ml9eDs6ODy9wxnY7TUDGBayYFlZry5MEpy2qpuJM1d4oqiV0JknBV8RIKrqlwpGKUJWsVB7qBdue6r6F7m0Acm9bH2TV2BN0kGqEUVpjxf8FCpwcpiv8FiWZca6ITuDcHXehiDFCb1-BbG6aGYDNLw6Q0jDVfaSR6ZyE7KVuoftnF-xNA5sC7b2D6l5Y5Pxx-i-bzHZ9S-PjZseHFCEklN_dXAyNvBhf3w4E2D_QTe36i_Q</recordid><startdate>200610</startdate><enddate>200610</enddate><creator>Li, Ying J.</creator><creator>Chung, Eugene H.</creator><creator>Rodriguez, Ryan T.</creator><creator>Firpo, Meri T.</creator><creator>Healy, Kevin E.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7SR</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>F28</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>200610</creationdate><title>Hydrogels as artificial matrices for human embryonic stem cell self-renewal</title><author>Li, Ying J. ; Chung, Eugene H. ; Rodriguez, Ryan T. ; Firpo, Meri T. ; Healy, Kevin E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4952-9ed460f47637935100c8a4f785c7f5c83870cbe7158d5be25936c1d434552d5e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>artificial extracellular matrices</topic><topic>Biocompatible Materials</topic><topic>Cell Line</topic><topic>Cells, Cultured</topic><topic>human embryonic stem cells</topic><topic>Humans</topic><topic>Hydrogels</topic><topic>interpenetrating networks</topic><topic>self-renewal</topic><topic>Stem Cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Ying J.</creatorcontrib><creatorcontrib>Chung, Eugene H.</creatorcontrib><creatorcontrib>Rodriguez, Ryan T.</creatorcontrib><creatorcontrib>Firpo, Meri T.</creatorcontrib><creatorcontrib>Healy, Kevin E.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of biomedical materials research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Ying J.</au><au>Chung, Eugene H.</au><au>Rodriguez, Ryan T.</au><au>Firpo, Meri T.</au><au>Healy, Kevin E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hydrogels as artificial matrices for human embryonic stem cell self-renewal</atitle><jtitle>Journal of biomedical materials research</jtitle><addtitle>J. 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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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