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Use of recombinant and synthetic peptides as attachment factors for cells on microcarriers

dc.contributor.authorVarani, Jamesen_US
dc.contributor.authorInman, Dennis R.en_US
dc.contributor.authorFligiel, Suzanne E. G.en_US
dc.contributor.authorHillegas, William J.en_US
dc.date.accessioned2006-09-08T20:31:56Z
dc.date.available2006-09-08T20:31:56Z
dc.date.issued1993-01en_US
dc.identifier.citationVarani, James; Inman, Dennis R.; Fligiel, Suzanne E. G.; Hillegas, William J.; (1993). "Use of recombinant and synthetic peptides as attachment factors for cells on microcarriers." Cytotechnology 13(2): 89-98. <http://hdl.handle.net/2027.42/42614>en_US
dc.identifier.issn0920-9069en_US
dc.identifier.issn1573-0778en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/42614
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=7764582&dopt=citationen_US
dc.description.abstractPolystyrene culture dishes and polystyrene microcarriers were coated with Pronectin-F and poly- l -lysine (polylysine), either alone or in combination. Pronectin-F is a recombinant peptide containing repeats of the RGD cell-attachment sequence from fibronectin. Polylysine is a polymer of l -lysine. Pronectin-F supported attachment of Madin-Darby Canine Kidney (MDCK) cells at concentrations as low as 0.025 μg/cm 2 of surface area. The cells rapidly spread after attachment. Polylysine at concentrations of 0.05–0.5 μg/cm 2 also supported cell attachment but cells did not rapidly spread after attachment to this substrate. Higher concentrations of polylysine could not be used because of toxicity. When the two peptides were used in conjunction, MDCK cells attached and spread at lower peptide concentrations than they did when either substrate was used alone. These findings suggest that recombinant Pronectin-F alone or in conjunction with a cationic polymer could be a useful replacement for materials such as gelatin or collagen which are currently used as microcarrier surfaces.en_US
dc.format.extent1044975 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers; Springer Science+Business Mediaen_US
dc.subject.otherLife Sciencesen_US
dc.subject.otherBiomedicine Generalen_US
dc.subject.otherBiochemistry, Generalen_US
dc.subject.otherProteomicsen_US
dc.subject.otherCell Biologyen_US
dc.subject.otherCollagenen_US
dc.subject.otherGelatinen_US
dc.subject.otherMDCKen_US
dc.subject.otherMicrocarrieren_US
dc.subject.otherPolylysineen_US
dc.subject.otherPronectin-Fen_US
dc.titleUse of recombinant and synthetic peptides as attachment factors for cells on microcarriersen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumThe Department of Pathology, The University of Michigan, 1301 Catherine Rd, Box 0602, 48109, Ann Arbor, Michigan, USA; The Department of Pathology, Wayne State University-VAMC, Allen Park, Michigan, USA; SoloHill Labs, Inc., Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumThe Department of Pathology, The University of Michigan, 1301 Catherine Rd, Box 0602, 48109, Ann Arbor, Michigan, USA; The Department of Pathology, Wayne State University-VAMC, Allen Park, Michigan, USA; SoloHill Labs, Inc., Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumThe Department of Pathology, The University of Michigan, 1301 Catherine Rd, Box 0602, 48109, Ann Arbor, Michigan, USA; The Department of Pathology, Wayne State University-VAMC, Allen Park, Michigan, USA; SoloHill Labs, Inc., Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumThe Department of Pathology, The University of Michigan, 1301 Catherine Rd, Box 0602, 48109, Ann Arbor, Michigan, USA; The Department of Pathology, Wayne State University-VAMC, Allen Park, Michigan, USA; SoloHill Labs, Inc., Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid7764582en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/42614/1/10616_2004_Article_BF00749935.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00749935en_US
dc.identifier.sourceCytotechnologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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