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Collagen I-Matrigel Scaffolds for Enhanced Schwann Cell Survival and Control of Three-Dimensional Cell Morphology

dc.contributor.authorDewitt, Daniel D.en_US
dc.contributor.authorKaszuba, Stephanie N.en_US
dc.contributor.authorThompson, Deanna M.en_US
dc.contributor.authorStegemann, Jan P.en_US
dc.date.accessioned2010-10-14T14:17:58Z
dc.date.available2010-10-14T14:17:58Z
dc.date.issued2009-10en_US
dc.identifier.citationDewitt, Daniel D.; Kaszuba, Stephanie N.; Thompson, Deanna M.; Stegemann, Jan P. (2009/02/20). "Collagen I-Matrigel Scaffolds for Enhanced Schwann Cell Survival and Control of Three-Dimensional Cell Morphology." Tissue Engineering Part A, 15(10): 2785-2793 <http://hdl.handle.net/2027.42/78114>en_US
dc.identifier.issn1937-3341en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/78114
dc.description.abstractWe report on the ability to control three-dimensional Schwann cell (SC) morphology using collagen I Matrigel composite scaffolds for neural engineering applications. SCs are supportive of nerve regeneration after injury, and it has recently been reported that SCs embedded in collagen I, a material frequently used in guidance channel studies, do not readily extend processes, instead adopting a spherical morphology indicative of little interaction with the matrix. We have modified collagen I matrices by adding Matrigel to make them more supportive of SCs and characterized these matrices and SC morphology in vitro. Incorporation of 10%, 20%, 35%, and 50% Matrigel by volume resulted in 2.4, 3.5, 3.7, and 4.2 times longer average SC process length after 14 days in culture than with collagen I only controls. Additionally, only 35% and 50% Matrigel constructs were able to maintain SC number over 14 days, whereas an 88% decrease in cells from initial seeding density was observed in collagen-only constructs over the same time period. Mechanical testing revealed that the addition of 50% Matrigel increased matrix stiffness from 6.4kPa in collagen I only constructs to 9.8kPa. Furthermore, second harmonic generation imaging showed that the addition of Matrigel resulted in non-uniform distribution of collagen I, and scanning electron microscope imaging illustrated distinct differences in the fibrillar structure of the different constructs. Collectively, this work lays a foundation for developing scaffolding materials that are concurrently supportive of neurons and SCs for future neural engineering applications.en_US
dc.format.extent377746 bytes
dc.format.extent3100 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherMary Ann Liebert, Inc.en_US
dc.titleCollagen I-Matrigel Scaffolds for Enhanced Schwann Cell Survival and Control of Three-Dimensional Cell Morphologyen_US
dc.typeArticleen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.identifier.pmid19231925en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/78114/1/ten.tea.2008.0406.pdf
dc.identifier.doi10.1089/ten.tea.2008.0406en_US
dc.identifier.sourceTissue Engineering Part Aen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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