Effect of Ischemic Neuronal Insults on Amyloid Precursor Protein Processing.
- Author:
Phil Hyu LEE
1
;
Eun Mi HWANG
;
Inhee MOOK-JUNG
;
Kyoon HUH
;
Il Saing CHOI
Author Information
1. Department of Neurology, Ajou University School of Medicine, Suwon, Korea. phisland@chol.net
- Publication Type:In Vitro ; Original Article
- Keywords:
Ischemic neuronal insult;
Amyloid precursor protein;
Beta-amyloid;
alpha-secretase;
beta-secretase;
gamma-secretase
- MeSH:
Alzheimer Disease;
Amyloid Precursor Protein Secretases;
Amyloid*;
Animals;
Brain Ischemia;
Cell Line;
Cells, Cultured;
Dementia, Vascular;
Diagnosis;
Humans;
Mice;
Mice, Transgenic;
Neuroblastoma;
Neurons*;
RNA, Messenger;
Stroke
- From:Journal of the Korean Neurological Association
2005;23(2):241-248
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: In spite of the different pathogenesis and exclusive respect in the diagnosis of Alzheimer's disease (AD) and vascular dementia (VaD), recent epidemiological and pathological studies indicates that ischemic stroke have an important role in the pathogenesis of both VaD and AD. However, the association of ischemic stroke and AD on the cellular and molecular level is still unknown. We evaluated the effect of ischemic neuronal insult on the regulation of amyloid precursor protein (APP) processing. METHODS: We used an in vitro model of cerebral ischemia (oxygen-glucose deprivation, OGD) to evaluate the effect of ischemic insult on the amyloidogenic and non-amyloidogenic pathways using human neuroblastoma cell line, SH-SY5Y, and primary cultured cells of Tg2576 APP transgenic mouse. RESULTS: Ischemic insult significantly increased the beta amyloid (A beta) production in the primary cultured cells of Tg2576 APP transgenic mice (p<0.001). A disintegrin and metalloprotease 10 (ADAM 10), a candidate of alpha-secretase, was markedly increased in the early stage of ischemic insult (up to 2 hours of OGD, p<0.001; 4 hours of OGD, p<0.05), which was followed by the decreased level of ADAM 10 expression in a later stage (p<0.001). However, the protein and mRNA expression of beta-site cleavage enzyme (BACE) and BACE activity were not significantly different between the group of ischemic insult and control. By contrast, the activity of gamma-secretase was significantly increased after 4 hours of ischemic insult, as compared to controls. CONCLUSIONS: This study demonstrates that the ischemic neuronal insults increase the production of A beta via activation of the amyloidogenic pathway, which may link the role of ischemic insults to the pathogenesis of AD.
