J Korean Neurol Assoc.  2005 Apr;23(2):241-248.

Effect of Ischemic Neuronal Insults on Amyloid Precursor Protein Processing

Affiliations
  • 1Department of Neurology, Ajou University School of Medicine, Suwon, Korea. phisland@chol.net
  • 2Department of Biochemistry, Seoul National University School of Medicine, Seoul, Korea.
  • 3Department of Neurology, Yonsei University College of Medicine, Seoul, Korea.

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.

Keyword

Ischemic neuronal insult; Amyloid precursor protein; Beta-amyloid; alpha-secretase; beta-secretase; gamma-secretase

MeSH Terms

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
Amyloid
Amyloid Precursor Protein Secretases
RNA, Messenger
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