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all-trans -Retinoic acid preserves viability of fibroblasts and keratinocytes in full-thickness human skin and fibroblasts in isolated dermis in organ culture

dc.contributor.authorVoorhees, John J.en_US
dc.contributor.authorVarani, Jamesen_US
dc.contributor.authorPerone, Patriciaen_US
dc.contributor.authorInman, Dennis R.en_US
dc.contributor.authorFligiel, Suzanne E. G.en_US
dc.date.accessioned2006-09-11T18:45:33Z
dc.date.available2006-09-11T18:45:33Z
dc.date.issued1994-10en_US
dc.identifier.citationVarani, James; Perone, Patricia; Fligiel, Suzanne E. G.; Inman, Dennis R.; Voorhees, John J.; (1994). " all-trans -Retinoic acid preserves viability of fibroblasts and keratinocytes in full-thickness human skin and fibroblasts in isolated dermis in organ culture." Archives of Dermatological Research 286(8): 443-447. <http://hdl.handle.net/2027.42/47248>en_US
dc.identifier.issn0340-3696en_US
dc.identifier.issn1432-069Xen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/47248
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=7864657&dopt=citationen_US
dc.description.abstractHuman dermal fibroblast and human epidermal keratinocyte survival was examined under various conditions in organ culture. Using cell recovery from organ-cultured tissue as the criterion, it was observed that no keratinocytes and few fibroblasts survived incubation for 10–12 days in serum-free basal medium containing a low level (0.15 m M ) of extracellular Ca 2+ . Increasing the extracellular Ca 2+ concentration to 1.4 m M or treating the tissue with 3 Μ M retinoic acid (RA) under low Ca 2+ conditions resulted in increased keratinocyte and fibroblast survival; the two treatments together were more effective than either treatment alone. The same treatments preserved fibroblast survival when pieces of isolated dermal tissue were incubated in organ culture and also supported fibroblast survival in monolayer culture. These findings indicate that recovery of keratinocytes and fibroblasts from skin after maintenance in organ culture provides a simple but definitive measure of the viability of the major cellular elements present in the tissue. These findings suggest that RA treatment enhances survival of both fibroblasts and keratinocytes and that these effects of RA can be seen at physiological Ca 2+ concentrations as well as at suboptimal levels of extracellular Ca 2+ . Finally, these results indicate that the dermis is a direct target of RA.en_US
dc.format.extent573366 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherCell Viabilityen_US
dc.subject.otherMedicine & Public Healthen_US
dc.subject.otherSkin Organ Cultureen_US
dc.subject.otherRetinoic Aciden_US
dc.subject.otherDermatologyen_US
dc.titleall-trans -Retinoic acid preserves viability of fibroblasts and keratinocytes in full-thickness human skin and fibroblasts in isolated dermis in organ cultureen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelDermatologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Dermatology, The University of Michigan Medical School, 48109, Ann Arbor, MI, USAen_US
dc.contributor.affiliationotherDepartment of Pathology, The Universtiy of Michigan Medical School, 1301 Catherine Road, Box 0602, 48109, Ann Arbor, MI, USAen_US
dc.contributor.affiliationotherDepartment of Pathology, VAMC - Wayne State University, 48102, Allen Park, MI, USAen_US
dc.contributor.affiliationotherDepartment of Pathology, The Universtiy of Michigan Medical School, 1301 Catherine Road, Box 0602, 48109, Ann Arbor, MI, USAen_US
dc.contributor.affiliationotherDepartment of Pathology, VAMC - Wayne State University, 48102, Allen Park, MI, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid7864657en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/47248/1/403_2004_Article_BF00371569.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00371569en_US
dc.identifier.sourceArchives of Dermatological Researchen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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