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          Institute: MPI für molekulare Zellbiologie und Genetik     Collection: Publikationen MPI-CBG 2006     Display Documents



ID: 311218.0, MPI für molekulare Zellbiologie und Genetik / Publikationen MPI-CBG 2006
Alzheimer's disease {beta}-amyloid peptides are released in association with exosomes
Authors:Rajendran, Lawrence; Honsho, Masanori; Zahn, Tobias R; Keller, Patrick; Geiger, Kathrin D; Verkade, Paul; Simons, Kai
Date of Publication (YYYY-MM-DD):2006
Title of Journal:Proceedings of the National Academy of Sciences, USA
Volume:103
Issue / Number:30
Start Page:11172
End Page:11177
Copyright:not available
Audience:Experts Only
Intended Educational Use:No
Abstract / Description:Although the exact etiology of Alzheimer's disease (AD) is a topic of debate, the consensus is that the accumulation of beta-amyloid (Abeta) peptides in the senile plaques is one of the hallmarks of the progression of the disease. The Abeta peptide is formed by the amyloidogenic cleavage of the amyloid precursor protein (APP) by beta- and gamma-secretases. The endocytic system has been implicated in the cleavages leading to the formation of Abeta. However, the identity of the intracellular compartment where the amyloidogenic secretases cleave and the mechanism by which the intracellularly generated Abeta is released into the extracellular milieu are not clear. Here, we show that beta-cleavage occurs in early endosomes followed by routing of Abeta to multivesicular bodies (MVBs) in HeLa and N2a cells. Subsequently, a minute fraction of Abeta peptides can be secreted from the cells in association with exosomes, intraluminal vesicles of MVBs that are released into the extracellular space as a result of fusion of MVBs with the plasma membrane. Exosomal proteins were found to accumulate in the plaques of AD patient brains, suggesting a role in the pathogenesis of AD.
External Publication Status:published
Document Type:Article
Communicated by:N. N.
Affiliations:MPI für molekulare Zellbiologie und Genetik
Identifiers:LOCALID:664
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