Adult human epidermal melanocytes for neurodegeneration research
dc.contributor.author | Papageorgiou, Nikolaos | * |
dc.contributor.author | Carpenter, Elizabeth | * |
dc.contributor.author | Scally, Andy J. | * |
dc.contributor.author | Tobin, Desmond J. | * |
dc.date.accessioned | 2014-07-08T17:19:25Z | |
dc.date.available | 2014-07-08T17:19:25Z | |
dc.date.issued | 2008 | |
dc.identifier.citation | Papageorgiou N, Carpenter E, Scally AJ et al (2008) Adult human epidermal melanocytes for neurodegeneration research. Neuroreport. 19(18): 1787-1791. | |
dc.identifier.uri | http://hdl.handle.net/10454/6387 | |
dc.description | No | |
dc.description.abstract | Neuronal 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.iso | en | en |
dc.subject | Neural crest-derived human epidermal melanocytes | |
dc.subject | Alzheimer's disease | |
dc.subject | Neuronal models | |
dc.subject | Amyloid precursor protein | |
dc.subject | APP | |
dc.title | Adult human epidermal melanocytes for neurodegeneration research | |
dc.status.refereed | No | |
dc.type | Article | |
dc.type.version | No full-text in the repository | |
dc.identifier.doi | https://doi.org/10.1097/WNR.0b013e3283193e82 | |
dc.openaccess.status | closedAccess |