FEBS Letters · 1994 · 146 citations · 28 references
Life SciencesNeurobiologyNeuroscienceGene ExpressionNeurodegenerationNeurogeneticsAlzheimer DiseaseAmyloid FormationMolecular Basis Of NeurodegenerationNeurodegenerative DiseasesNeurodegenerative DisordersAmyloid Beta PeptidesAmyloidogenic PeptidesAmyloidogenic ProteinsApp MutationsHereditary AmyloidosisMutationPrecursor Protein MaturationTransgenic Cell Lines
Cell lines transfected with the Swedish Alzheimer's disease amyloid precursor protein APP670/671 mutation release significantly more beta-amyloid than wild-type cells. Citron et al. [Proc. Natl. Acad. Sci. USA (1994) in press] have recently shown that fibroblasts carrying the APP670/671 mutation also release more beta-amyloid than control cells [1]. The present study confirms a ca. threefold increase in beta-amyloid release from mutation-bearing fibroblasts. APP mRNA levels did not differ between mutation-bearing and control cells, although mutation-bearing fibroblasts contained significantly more APP751/770 than controls. Mild stress decreased beta-amyloid secretion and increased APP751/770 levels in all cell lines. In conclusion, the proportion of APP committed to amyloidogenic processing is increased in fibroblasts from family members with the APP670/671 mutation, and this mutation may also compromise the APP stress response.
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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
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The precursor of Alzheimer's disease amyloid A4 protein resembles a cell-surface receptor
Jie Kang, Hans-Georg Lemaire, Axel Unterbeck et al. · Nature · 1987 · 4.6K citations