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PMID: 12445809 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

alpha- and beta-secretase: profound changes in Alzheimer's disease.

Biochemical and biophysical research communications ·Vol. 299 ·No. 3 ·2002-12-06 ·Pages 373-6

Tyler SJ, Dawbarn D, Wilcock GK, Allen SJ

Abstract

The amyloid plaque, a neuropathological hallmark of Alzheimer's disease, is produced by the deposition of beta-amyloid (Abeta) peptide, which is cleaved from Amyloid Precursor Protein (APP) by the enzyme beta-secretase. Only small amounts of Abeta form in normal brain; more typically this is precluded by the processing of APP by alpha-secretase. Here, we describe a decrease in alpha-secretase (81% of normal) and a large increase in beta-secretase activity (185%) in sporadic Alzheimer's disease temporal cortex. Since alpha-secretase is present principally in neurons known to be vulnerable in Alzheimer's disease, and there is known competition between alpha- and beta-secretase for the substrate APP, it is significant that the majority of Alzheimer samples tested here were low in alpha-secretase. Eighty percent of Alzheimer brains examined had an increase in beta-secretase, a decrease in alpha-secretase, or both; which may account for the means by which the majority of people develop Alzheimer's disease.

MeSH Terms
Aged Aged, 80 and over Alzheimer Disease/metabolism,physiopathology Amyloid Precursor Protein Secretases Amyloid beta-Protein Precursor/metabolism Apolipoproteins E/genetics Aspartic Acid Endopeptidases/metabolism Choline O-Acetyltransferase/metabolism Endopeptidases/metabolism Humans Statistics as Topic Temporal Lobe/enzymology
Chemicals
Amyloid beta-Protein Precursor Apolipoproteins E Choline O-Acetyltransferase Amyloid Precursor Protein Secretases Endopeptidases Aspartic Acid Endopeptidases BACE1 protein, human
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Tyler Susan J
Molecular Neurobiology Unit, URCN (Care of the Elderly) University of Bristol, Bristol Royal Infirmary, Bristol, UK.
Dawbarn David
Wilcock Gordon K
Allen Shelley J
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
2002-12-06
Pages
373-6
Language
English
Region
United States
NLM ID
0372516
Subset
IM
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