Down-regulation of the ATP-binding cassette transporter 2 (Abca2) reduces amyloid-β production by altering Nicastrin maturation and intracellular localization.

Michaki V., Guix FX., Vennekens K., Munck S., Dingwall C., Davis JB., Townsend DM., Tew KD., Feiguin F., De Strooper B., Dotti CG., Wahle T.

Clinical, pharmacological, biochemical, and genetic evidence support the notion that alteration of cholesterol homeostasis strongly predisposes to Alzheimer disease (AD). The ATP-binding cassette transporter-2 (Abca2), which plays a role in intracellular sterol trafficking, has been genetically linked to AD. It is unclear how these two processes are related. Here we demonstrate that down-regulation of Abca2 in mammalian cells leads to decreased amyloid-β (Aβ) generation. In vitro studies revealed altered γ-secretase complex formation in Abca2 knock-out cells due to the altered levels, post-translational modification, and subcellular localization of Nicastrin. Reduced Abca2 levels in mammalian cells in vitro, in Drosophila melanogaster and in mice resulted in altered γ-secretase processing of APP, and thus Aβ generation, without affecting Notch cleavage.

DOI

10.1074/jbc.M111.288258

Type

Journal article

Publication Date

2012-01-06T00:00:00+00:00

Volume

287

Pages

1100 - 1111

Total pages

11

Keywords

ATP-Binding Cassette Transporters, Alzheimer Disease, Amyloid Precursor Protein Secretases, Amyloid beta-Protein Precursor, Animals, Down-Regulation, Drosophila Proteins, Drosophila melanogaster, HEK293 Cells, Humans, Membrane Glycoproteins, Mice, Nerve Tissue Proteins, Rats

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