Distinct amyloid precursor protein processing machineries of the olfactory system

被引:16
作者
Kim, Jae Yeon [1 ]
Rasheed, Ameer [1 ]
Yoo, Seung-Jun [1 ,2 ]
Kim, So Yeun [1 ,2 ]
Cho, Bongki [1 ,2 ]
Son, Gowoon [1 ]
Yu, Seong-Woon [1 ]
Chang, Keun-A. [3 ]
Suh, Yoo-Hun [3 ]
Moon, Cheil [1 ,2 ]
机构
[1] Daegu Gyeungbuk Inst Sci & Technol, Grad Sch, Dept Brain & Cognit Sci, 333 Techno Jung Ang Daero, Daegu 711873, South Korea
[2] Daegu Gyeungbuk Inst Sci & Technol, Convergence Res Adv Ctr Olfact, Daegu, South Korea
[3] Gachon Med Sch, Sch Med, Dept Pharmacol, Incheon, South Korea
基金
新加坡国家研究基金会;
关键词
Alzheimer's disease(AD); Amyloid precursor protein(APP); Olfactory system; Olfactory epithelium(OE); gamma-Secretase; Presenilin; ALZHEIMERS-DISEASE; GAMMA-SECRETASE; INTRAMEMBRANE PROTEOLYSIS; MOUSE MODEL; A-BETA; MEMORY; EXPRESSION; PLAQUES;
D O I
10.1016/j.bbrc.2017.10.153
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:533 / 538
页数:6
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