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PMID: 15548589 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Intracellular Abeta42 activates p53 promoter: a pathway to neurodegeneration in Alzheimer's disease.

Ohyagi Y, Asahara H, Chui DH, Tsuruta Y, Sakae N, Miyoshi K, Yamada T, Kikuchi H, Taniwaki T, Murai H, Ikezoe K, Furuya H, Kawarabayashi T, Shoji M, Checler F, Iwaki T, Makifuchi T, Takeda K, Kira J, Tabira T

Abstract

The amyloid beta-protein (Abeta) ending at 42 plays a pivotal role in Alzheimer's disease (AD). We have reported previously that intracellular Abeta42 is associated with neuronal apoptosis in vitro and in vivo. Here, we show that intracellular Abeta42 directly activated the p53 promoter, resulting in p53-dependent apoptosis, and that intracellular Abeta40 had a similar but lesser effect. Moreover, oxidative DNA damage induced nuclear localization of Abeta42 with p53 mRNA elevation in guinea-pig primary neurons. Also, p53 expression was elevated in brain of sporadic AD and transgenic mice carrying mutant familial AD genes. Remarkably, accumulation of both Abeta42 and p53 was found in some degenerating-shape neurons in both transgenic mice and human AD cases. Thus, the intracellular Abeta42/p53 pathway may be directly relevant to neuronal loss in AD. Although neurotoxicity of extracellular Abeta is well known and synaptic/mitochondrial dysfunction by intracellular Abeta42 has recently been suggested, intracellular Abeta42 may cause p53-dependent neuronal apoptosis through activation of the p53 promoter; thus demonstrating an alternative pathogenesis in AD.

MeSH Terms
Aged Aged, 80 and over Alzheimer Disease/metabolism,pathology Amyloid beta-Peptides/metabolism,physiology Amyloid beta-Protein Precursor/genetics Animals Apoptosis/genetics,physiology Brain/cytology,metabolism,pathology Brain Chemistry/genetics Cells, Cultured Cytosol/chemistry DNA/metabolism Female Fetus Genes, p53/genetics Guinea Pigs Heat-Shock Response/genetics Humans Hydrogen Peroxide/pharmacology Intracellular Space/chemistry,metabolism,pathology Leucine/genetics Male Membrane Proteins/genetics Mice Mice, Mutant Strains Mice, Transgenic Mutation, Missense/genetics Nerve Degeneration/metabolism,pathology Neuroblastoma/pathology Neurons/chemistry,metabolism Peptide Fragments/metabolism,physiology Presenilin-1 Promoter Regions, Genetic/genetics,physiology Protein Binding RNA, Messenger/genetics,metabolism Response Elements/physiology Tumor Cells, Cultured Tumor Suppressor Protein p53/biosynthesis Valine/genetics
Chemicals
Amyloid beta-Peptides Amyloid beta-Protein Precursor Membrane Proteins PSEN1 protein, human Peptide Fragments Presenilin-1 RNA, Messenger Tumor Suppressor Protein p53 amyloid beta-protein (1-42) DNA Hydrogen Peroxide Leucine Valine
Authors & Affiliations
20 authors, click to expand affiliations / ORCID
Ohyagi Yasumasa
Department of Neurology, Neurological Institute, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan. ohyagi@neuro.med.kyushu-u.ac.jp
Asahara Hideaki
Chui De-Hua
Tsuruta Yuko
Sakae Nobutaka
Miyoshi Katsue
Yamada Takeshi
Kikuchi Hitoshi
Taniwaki Takayuki
Murai Hiroyuki
Ikezoe Koji
Furuya Hirokazu
Kawarabayashi Takeshi
Shoji Mikio
Checler Frederic
Iwaki Toru
Makifuchi Takao
Takeda Kazuya
Kira Jun-ichi
Tabira Takeshi
Article Info
Journal
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
Abbr.
FASEB J
ISSN
1530-6860
Published
2005-02-00
Epub
2004-00-17
Pages
255-7
Language
English
Region
United States
NLM ID
8804484
Subset
IM
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