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Substrate-dependent differences in production of extracellular matrix molecules by squamous carcinoma cells and diploid fibroblasts

dc.contributor.authorVarani, Jamesen_US
dc.contributor.authorFligiel, Suzanne E. G.en_US
dc.contributor.authorInman, Dennis R.en_US
dc.contributor.authorHelmreich, David L.en_US
dc.contributor.authorBendelow, Matthew J.en_US
dc.contributor.authorHillegas, William A.en_US
dc.date.accessioned2006-04-28T16:29:58Z
dc.date.available2006-04-28T16:29:58Z
dc.date.issued1989-04-20en_US
dc.identifier.citationVarani, James; Fligiel, Suzanne E. G.; Inman, Dennis R.; Helmreich, David L.; Bendelow, Matthew J.; Hillegas, William (1989)."Substrate-dependent differences in production of extracellular matrix molecules by squamous carcinoma cells and diploid fibroblasts." Biotechnology and Bioengineering 33(10): 1235-1241. <http://hdl.handle.net/2027.42/37897>en_US
dc.identifier.issn0006-3592en_US
dc.identifier.issn1097-0290en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/37897
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=18587855&dopt=citationen_US
dc.description.abstractTwo human squamous carcinoma cell lines and human diploid fibroblasts were examined for the production of extracellular matrix (ECM) molecules including fibronectin (FN), laminin (LN), and thrombospondin (TSP) when grown on a number of different substrates. The substrates used included glass, plastic, collagen (gelatin), and DEAE-dextran. Levels of TSP as indicated by enzyme-linked immunosorbent assay did not vary significantly as a function of substrate. In contrast, LN levels in the culture medium were significantly decreased when the cells were grown on DEAE-dextran or collagen-linked dextran as compared to the other substrates. FN levels were slightly lower in the culture medium of the cells grown on DEAE-dextran. Biosynthetic labeling followed by immunoprecipitation indicated that the reduction in LN was due, in part, to decreased biosynthesis. Previous studies have indicated that LN influences the behavior of epithelial cells in culture and that the cells, themselves, are a major source of the LN. The differences in LN production noted here indicate that the production of this ECM component is influenced by the substratum on which the cells are grown. These differences could contribute to alterations in biological properties that are known to be influenced by the substratum.en_US
dc.format.extent884142 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherChemistryen_US
dc.subject.otherBiochemistry and Biotechnologyen_US
dc.titleSubstrate-dependent differences in production of extracellular matrix molecules by squamous carcinoma cells and diploid fibroblastsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbsecondlevelEcology and Evolutionary Biologyen_US
dc.subject.hlbsecondlevelMathematicsen_US
dc.subject.hlbsecondlevelNatural Resources and Environmenten_US
dc.subject.hlbsecondlevelStatistics and Numeric Dataen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelSocial Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of pathology, University of Michigan Medical School, Ann Arbor, Michigan 48109, Solohill Engineering, Inc., Ann Arbor, Michigan 48104, and Department of Pathology, VAMC-Wayne State University, Allen Park, Michigan 48101 ; Department of Pathology, Univerrsity of Michigan Medical School, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumDepartment of pathology, University of Michigan Medical School, Ann Arbor, Michigan 48109, Solohill Engineering, Inc., Ann Arbor, Michigan 48104, and Department of Pathology, VAMC-Wayne State University, Allen Park, Michigan 48101en_US
dc.contributor.affiliationumDepartment of pathology, University of Michigan Medical School, Ann Arbor, Michigan 48109, Solohill Engineering, Inc., Ann Arbor, Michigan 48104, and Department of Pathology, VAMC-Wayne State University, Allen Park, Michigan 48101en_US
dc.contributor.affiliationumDepartment of pathology, University of Michigan Medical School, Ann Arbor, Michigan 48109, Solohill Engineering, Inc., Ann Arbor, Michigan 48104, and Department of Pathology, VAMC-Wayne State University, Allen Park, Michigan 48101en_US
dc.contributor.affiliationumDepartment of pathology, University of Michigan Medical School, Ann Arbor, Michigan 48109, Solohill Engineering, Inc., Ann Arbor, Michigan 48104, and Department of Pathology, VAMC-Wayne State University, Allen Park, Michigan 48101en_US
dc.contributor.affiliationumDepartment of pathology, University of Michigan Medical School, Ann Arbor, Michigan 48109, Solohill Engineering, Inc., Ann Arbor, Michigan 48104, and Department of Pathology, VAMC-Wayne State University, Allen Park, Michigan 48101en_US
dc.identifier.pmid18587855en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/37897/1/260331003_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/bit.260331003en_US
dc.identifier.sourceBiotechnology and Bioengineeringen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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