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A Cell Biological Perspective on Alzheimer's Disease
Abstract
▪ Abstract The amyloid precursor protein and the proteases cleaving this protein are important players in the pathogenesis of Alzheimer's disease via the generation of the amyloid peptide. Physiologically, the amyloid precursor protein is implied in axonal vesicular trafficking and the proteases are implicated in developmentally important signaling pathways, most significantly those involving regulated intramembrane proteolysis or RIP. We discuss the cell biology behind the amyloid and tangle hypothesis for Alzheimer's disease, drawing on the many links to the fields of cell biology and developmental biology that have been established in the recent years.
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Aβ is generated by sequential cleavage of APP by β-secretase and γ-secretase.
“The -amyloid peptide (A) is a major component of Alzheimer disease (AD)-associated senile plaques and is generated by sequential cleavage of the -amyloid precursor protein (APP) by -secretase (BACE1) and ␥-secretase.”
From GGA1 Is Expressed in the Human Brain and Affects the Generation of Amyloid β-Peptide (2006) · cites this paper as Annaert and de Strooper, 2002
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Metadata
- Authors
- Annaert, W., & De Strooper, B.
- Affiliations
- Neuronal Cell Biology Laboratory, Flanders Interuniversity Institute for Biotechnology (VIB) and Catholic University of Leuven, Center for Human Genetics Herestraat 49, 3000 Leuven Belgium;
- Venue
- Annual Review of Cell and Developmental Biology
- Publisher
- Annual Reviews
- Published
- 2002-11
- Volume
- 18
- Issue
- 1
- Pages
- 25-51
- ISSN
- 1081-0706
- 1530-8995
- Cited by
- 182
- References
- 13
- Language
- en
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