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Modulation of adhesive properties of DEAE-dextran with laminin

dc.contributor.authorVarani, Jamesen_US
dc.contributor.authorFligiel, Suzanne E. G.en_US
dc.contributor.authorInman, Dennis R.en_US
dc.contributor.authorBeals, Theodore F.en_US
dc.contributor.authorHillegas, William J.en_US
dc.date.accessioned2006-04-28T16:35:46Z
dc.date.available2006-04-28T16:35:46Z
dc.date.issued1995-08en_US
dc.identifier.citationVarani, James; Fligiel, Suzanne E. G.; Inman, Dennis R.; Beals, Ted F.; Hillegas, William J. (1995)."Modulation of adhesive properties of DEAE-dextran with laminin." Journal of Biomedical Materials Research 29(8): 993-997. <http://hdl.handle.net/2027.42/38011>en_US
dc.identifier.issn0021-9304en_US
dc.identifier.issn1097-4636en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/38011
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=7593043&dopt=citationen_US
dc.description.abstractHuman squamous epithelial cells produce lower amounts of laminin and fibronectin when cultured on DEAE-dextran than when cultured on gelatin-coated polystyrene ( Biotechnol. Bioeng. , 33:1235). The epithelial cells also spread much more slowly on DEAE-dextran than they do on gelatincoated polystyrene. To determine if the low level of matrix production by cells grown on DEAE-dextran contributed to the slowness of cell spreading on this substrate, microcarriers made from DEAE-dextran were treated with exogenous laminin (10 Μg/cm 2 of surface area) and then examined for ability to support cell adhesion. Squamous epithelial cells spread as rapidly on the laminin-treated DEAE-dextran as they did on gelatin-coated polystyrene (much more rapidly than on untreated DEAE-dextran). This indicates (1) that laminin can bind to DEAE-dextran in a fashion that is biologically usable by anchorage-dependent cells, and (2) that when laminin is bound to DEAE-dextran, the failure of squamous epithelial cells to rapidly spread is overcome. These data support the hypothesis that failure of the cells to synthesize an intact extracellular matrix on DEAE-dextran is responsible, at least in part, for the slowness with which cells spread on this substrate. © 1995 John Wiley & Sons, Inc.en_US
dc.format.extent501326 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.subject.otherChemistryen_US
dc.subject.otherPolymer and Materials Scienceen_US
dc.titleModulation of adhesive properties of DEAE-dextran with lamininen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbsecondlevelBiomedical Engineeringen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pathology, University of Michigan, Ann Arbor, Michigan 48109 ; Department of Pathology, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumDepartment of Pathology, WAMC-University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationotherDepartment of Pathology, VAMC-Wayne State University, Allen Park, Michigan 48101en_US
dc.contributor.affiliationotherDepartment of Pathology, VAMC-Wayne State University, Allen Park, Michigan 48101en_US
dc.contributor.affiliationotherSolohill Labs, Inc., Ann Arbor, Michigan 48104en_US
dc.identifier.pmid7593043en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/38011/1/820290811_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/jbm.820290811en_US
dc.identifier.sourceJournal of Biomedical Materials Researchen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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