期刊
NEUROBIOLOGY OF AGING
卷 25, 期 10, 页码 1263-1272出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.neurobiolaging.2004.02.027
关键词
endocytosis; early endosome; a beta peptide; Alzheimer's disease; Down syndrome; cellular trafficking; amyloid precursor protein processing; neuropathology; proteolysis
Early endosomes are a major site of amyloid precursor protein (APP) processing and a convergence point for molecules of pathologic relevance to Alzheimer's disease (AD). Neuronal endosome enlargement, reflecting altered endocytic function, is a disease-specific response that develops years before the earliest stage of AD and Down syndrome (DS). We examined how endocytic dysfunction is related to Abeta accumulation and distribution in early stage AD and DS. We found by ELISA and immunocytochernistry that the appearance of enlarged endosomes coincided with an initial rise in soluble Abeta40 and Abeta42 peptides, which preceded amyloid deposition. Double-immunofluorescence using numerous Abeta antibodies showed that intracellular Abeta localized principally to rab5-positive endosomes in neurons from AD brains and was prominent in enlarged endosomes. Abeta was not detectable in neurons from normal controls and was diminished after amyloid deposition in neuropathologically confirmed AD. These studies support growing evidence that endosomal pathology contributes significantly to Abeta overproduction and accumulation in sporadic AD and in AD associated with DS and may signify earlier disease-relevant disturbances of the signaling functions of endosomes. (C) 2004 Elsevier Inc. All rights reserved.
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