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dc.contributor.authorPapageorgiou, Nikolaos*
dc.contributor.authorCarpenter, Elizabeth*
dc.contributor.authorScally, Andy J.*
dc.contributor.authorTobin, Desmond J.*
dc.date.accessioned2014-07-08T17:19:25Z
dc.date.available2014-07-08T17:19:25Z
dc.date.issued2008
dc.identifier.citationPapageorgiou N, Carpenter E, Scally AJ et al (2008) Adult human epidermal melanocytes for neurodegeneration research. Neuroreport. 19(18): 1787-1791.
dc.identifier.urihttp://hdl.handle.net/10454/6387
dc.descriptionNo
dc.description.abstractNeuronal models for Alzheimer's disease research frequently have limitations as a result of their nonhuman origin and/or transformed state. Here we examined the potential of readily accessible neural crest-derived human epidermal melanocytes isolated from elderly individuals as a model system for Alzheimer's disease research. The amyloidogenic isoforms of amyloid precursor protein (APP; isoforms APP751/770) and amyloid beta (A¿)1¿40 were detected in epidermal melanocytes using immunocytochemistry and western blotting. Incubation of epidermal melanocytes with aggregated A¿1¿40 peptide caused a concentration-dependent reduction in cell viability, whereas age-matched dermal fibroblasts remained unaffected. These findings suggest that epidermal melanocytes from elderly donors are capable of amyloidogenesis and are sensitive to A¿1¿40 cytotoxicity. Thus, these cells may provide a readily accessible human cell model for Alzheimer's disease research.
dc.language.isoenen
dc.subjectNeural crest-derived human epidermal melanocytes
dc.subjectAlzheimer's disease
dc.subjectNeuronal models
dc.subjectAmyloid precursor protein
dc.subjectAPP
dc.titleAdult human epidermal melanocytes for neurodegeneration research
dc.status.refereedNo
dc.typeArticle
dc.type.versionNo full-text in the repository
dc.identifier.doihttps://doi.org/10.1097/WNR.0b013e3283193e82
dc.openaccess.statusclosedAccess


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