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A betaPP peptide carboxyl-terminal to Abeta is neurotoxic.
Marcon, G; Giaccone, G; Canciani, B; Cajola, L; Rossi, G; De Gioia, L; Salmona, M; Bugiani, O; Tagliavini, F.
Afiliación
  • Marcon G; Division of Neuropathology, Istituto Nazionale Neurologico Carlo Besta, Italy.
Am J Pathol ; 154(4): 1001-7, 1999 Apr.
Article en En | MEDLINE | ID: mdl-10233838
Extracellular Abeta-amyloid and intraneuronal paired helical filaments (PHFs) composed of tau protein are the neuropathological hallmark of Alzheimer's disease. Abeta is a 39- to 43-residue peptide derived by cleavage of a 695- to 770-amino-acid membrane-associate glycoprotein (termed beta-protein precursor, betaPP). Following the observation that an antiserum to an epitope located between residues 713 and 723 of betaPP770 (ie, the transmembrane region of the betaPP distal to Abeta) labels PHFs and that a synthetic peptide homologous to residues 713 to 730 of betaPP770 (betaPP713-730) is highly fibrillogenic and interacts with tau in vitro, it has been hypothesized that betaPP fragments other than Abeta may feature in the pathogenesis of Alzheimer's disease concurring with neuronal degeneration. To investigate this issue, we have analyzed the effects of the exposure of primary neuronal cultures to the synthetic peptide betaPP713-730. Cultures were prepared from rat hippocampus on embryonic day 17 and incubated with the peptide at 2.5 to 30 micromol/L concentration for 1 to 4 days. Cell viability was compared with that of control cultures exposed to a scrambled sequence of the peptide. A 4-day exposure to 20 micromol/L betaPP713-730 resulted in almost complete neuronal loss, whereas no changes were observed with the scrambled peptide. Degenerating neurons showed DNA fragmentation by agarose gel electrophoresis and apoptotic changes by light and electron microscopy. These findings support the view that betaPP sequences other than Abeta may play a role in nerve cell degeneration in Alzheimer's disease.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fragmentos de Péptidos / Precursor de Proteína beta-Amiloide / Neuronas Límite: Animals Idioma: En Revista: Am J Pathol Año: 1999 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fragmentos de Péptidos / Precursor de Proteína beta-Amiloide / Neuronas Límite: Animals Idioma: En Revista: Am J Pathol Año: 1999 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Estados Unidos