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dc.contributor.authorEvangelisti, Elisa
dc.date.accessioned2022-05-31T10:21:16Z
dc.date.available2022-05-31T10:21:16Z
dc.date.issued2013
dc.identifierONIX_20220531_9788866554455_390
dc.identifier.issn2612-8020
dc.identifier.urihttps://library.oapen.org/handle/20.500.12657/55106
dc.description.abstractAlzheimer’s disease (AD) is a common form of dementia characterized by the formation of extracellular senile plaques composed of aggregated amyloid peptide (Aβ). The present studies provide evidence that: cell resistance to amyloid toxicity is related to lipid raft cholesterol content. Cholesterol and GM1, affect the susceptibility of Familial Alzheimer’s Disease (FAD) broblasts to Aβ42 oligomers in opposite ways, by modulating amyloid binding to lipid rafts and its subsequent toxic effects. The degree of toxicity of the oligomeric species results from a complex interplay between the structural and physicochemical features of both the oligomers and the cellular membrane. Neuronal differentiation of human mesenchymal stromal cells increases their resistance to Aβ42 aggregate toxicity.
dc.languageEnglish
dc.relation.ispartofseriesPremio Tesi di Dottorato
dc.titleStructural and functional aspects of membranes
dc.title.alternativeThe involvement of lipid rafts in Alzheimer’s disease pathogenesis. The interplay between protein oligomers and plasma membrane physicochemical features in determining cytotoxicity
dc.typebook
oapen.identifier.doi10.36253/978-88-6655-445-5
oapen.relation.isPublishedBybf65d21a-78e5-4ba2-983a-dbfa90962870
oapen.relation.isbn9788866554455
oapen.relation.isbn9788866554448
oapen.relation.isbn9788892734715
oapen.series.number31
oapen.pages152
oapen.place.publicationFlorence


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