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Recent reports have focused on the potential role of amyloid oligomers or protofibrils as a neurotoxic form of amyloid-\u03b2 (A\u03b2) and related amyloid aggregates. Here we describe studies indicating that overt neuronal cell death mediated by A\u03b2<jats:sub>1-40<\/jats:sub>is critically dependent on ongoing A\u03b2<jats:sub>1-40<\/jats:sub>polymerization and is not mediated by a single stable species of neurotoxic aggregate. The extent and rate of neuronal cell death can be controlled by conditions that alter the rate of A\u03b2 polymerization. The results presented here indicate that protofibrils and oligomeric forms of A\u03b2 most likely generate neuronal cell death through a nucleation-dependent process rather than acting as direct neurotoxic ligands. These findings bring into question the use of the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide formazan assay (MTT assay) as a reporter of A\u03b2-mediated neuronal cell death and suggest that diffusible A\u03b2 protofibrils and oligomers more likely mediate subtle alterations of synaptic function and long-term potentiation rather than overt neuronal cell death. These results have been extended to A\u03b2<jats:sub>1-42<\/jats:sub>, the non-A\u03b2 component of Alzheimer's disease amyloid plaques, and human amylin, suggesting that nucleation-dependent polymerization is a common mechanism of amyloid-mediated neuronal cell death. Our findings indicate that ongoing amyloid fibrillogenesis may be an essential mechanistic process underlying the pathogenesis associated with protein aggregation in amyloid disorders.<\/jats:p>","DOI":"10.1523\/jneurosci.2381-04.2005","type":"journal-article","created":{"date-parts":[[2005,2,2]],"date-time":"2005-02-02T20:40:28Z","timestamp":1107376828000},"page":"1071-1080","source":"Crossref","is-referenced-by-count":196,"title":["Nucleation-Dependent Polymerization Is an Essential Component of Amyloid-Mediated Neuronal Cell 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