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Distinct amyloid precursor protein processing machineries of the olfactory system

Authors
Kim, Jae YeonRasheed, AmeerYoo, Seung-JunKim, So YeunCho, BongkiSon, GowoonYu, Seong-WoonChang, Keun-A.Suh, Yoo-HunMoon, Cheil
Issue Date
1-Jan-2018
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
Alzheimer' s disease(AD); Amyloid precursor protein(APP); Olfactory system; Olfactory epithelium(OE); gamma-Secretase; Presenilin
Citation
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.495, no.1, pp.533 - 538
Journal Title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Volume
495
Number
1
Start Page
533
End Page
538
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/4178
DOI
10.1016/j.bbrc.2017.10.153
ISSN
0006-291X
Abstract
Processing of amyloid precursor protein (APP) occurs through sequential cleavages first by beta-secretase and then by the gamma-secretase complex. However, abnormal processing of APP leads to excessive production of beta-amyloid (A beta) in the central nervous system (CNS), an event which is regarded as a primary cause of Alzheimer's disease (AD). In particular, gene mutations of the gamma-secretase complex-which contains presenilin 1 or 2 as the catalytic core-could trigger marked All accumulation. Olfactory dysfunction usually occurs before the onset of typical AD-related symptoms (eg, memory loss or muscle retardation), suggesting that the olfactory system may be one of the most vulnerable regions to AD. To date however, little is known about why the olfactory system is affected so early by AD prior to other regions. Thus, we examined the distribution of secretases and levels of APP processing in the olfactory system under either healthy or pathological conditions. Here, we show that the olfactory system has distinct APP processing machineries. In particular, we identified higher expressions levels and activity of gamma-secretase in the olfactory epithelium (OE) than other regions of the brain. Moreover, APP c-terminal fragments (CTF) are markedly detected. During AD progression, we note increased expression of presenilin2 of gamma-secretases in the OE, not in the OB, and show that neurotoxic A beta*56 accumulates more quickly in the OE. Taken together, these results suggest that the olfactory system has distinct APP processing machineries under healthy and pathological conditions. This finding may provide a crucial understanding of the unique APP-processing mechanisms in the olfactory system, and further highlights the correlation between olfactory deficits and AD symptoms. (C) 2017 Elsevier Inc. All rights reserved.
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