• Medientyp: E-Artikel
  • Titel: Mechanism of Amyloid Plaque Formation Suggests an Intracellular Basis of Aβ Pathogenicity
  • Beteiligte: Friedrich, Ralf P.; Tepper, Katharina; Rönicke, Raik; Soom, Malle; Westermann, Martin; Reymann, Klaus; Kaether, Christoph; Fändrich, Marcus; Eisenberg, David S.
  • Erschienen: National Academy of Sciences, 2010
  • Erschienen in: Proceedings of the National Academy of Sciences of the United States of America, 107 (2010) 5, Seite 1942-1947
  • Sprache: Englisch
  • ISSN: 0027-8424
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  • Beschreibung: <p>The formation of extracellular amyloid plaques is a common pathobiochemical event underlying several debilitating human conditions, including Alzheimer's disease (AD). Considerable evidence implies that AD damage arises primarily from small oligomeric amyloid forms of Aβ peptide, but the precise mechanism of pathogenicity remains to be established. Using a cell culture system that reproducibly leads to the formation of Alzheimer's Aβ amyloid plaques, we show here that the formation of a single amyloid plaque represents a template-dependent process that critically involves the presence of endocytosis-or phagocytosis-competent cells. Internalized Aβ peptide becomes sorted to multivesicular bodies where fibrils grow out, thus penetrating the vesicular membrane. Upon plaque formation, cells undergo cell death and intracellular amyloid structures become released into the extracellular space. These data imply a mechanism where the pathogenic activity of Aβ is attributed, at least in part, to intracellular aggregates.</p>
  • Zugangsstatus: Freier Zugang