Prostate stem cell antigen interacts with nicotinic acetylcholine receptors and is affected in Alzheimer's disease

被引:32
|
作者
Jensen, Majbrit M. [1 ]
Arvaniti, Maria [1 ]
Mikkelsen, Jens D. [1 ]
Michalski, Dominik [2 ]
Pinborg, Lars H. [1 ,3 ]
Hartig, Wolfgang [4 ]
Thomsen, Morten S. [1 ]
机构
[1] Rigshosp, Copenhagen Univ Hosp, Neurobiol Res Unit, DK-2100 Copenhagen, Denmark
[2] Univ Leipzig, Dept Neurol, D-04109 Leipzig, Germany
[3] Rigshosp, Copenhagen Univ Hosp, Epilepsy Clin, DK-2100 Copenhagen, Denmark
[4] Univ Leipzig, Paul Flechsig Inst Brain Res, D-04109 Leipzig, Germany
关键词
Alzheimer's disease; Nicotinic acetylcholine receptor; Frontal cortex; Lynx; PSCA; Lypd6; HUMAN-BRAIN; PROTOTOXIN LYNX1; MEMORY DEFICITS; PC12; CELLS; IN-VIVO; A-BETA; PROTEINS; KINASE; ASSOCIATION; SUBUNIT;
D O I
10.1016/j.neurobiolaging.2015.01.001
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Alzheimer's disease (AD) is a neurodegenerative disorder involving impaired cholinergic neurotransmission and dysregulation of nicotinic acetylcholine receptors (nAChRs). Ly-6/neurotoxin (Lynx) proteins have been shown to modulate cognition and neural plasticity by binding to nAChR subtypes and modulating their function. Hence, changes in nAChR regulatory proteins such as Lynx proteins could underlie the dysregulation of nAChRs in AD. Using Western blotting, we detected bands corresponding to the Lynx proteins prostate stem cell antigen (PSCA) and Lypd6 in human cortex indicating that both proteins are present in the human brain. We further showed that PSCA forms stable complexes with the alpha 4 nAChR subunit and decreases nicotine-induced extracellular-signal regulated kinase phosphorylation in PC12 cells. In addition, we analyzed protein levels of PSCA and Lypd6 in postmortem tissue of medial frontal gyrus from AD patients and found significantly increased PSCA levels (approximately 70%). In contrast, no changes in Lypd6 levels were detected. In concordance with our findings in AD patients, PSCA levels were increased in the frontal cortex of triple transgenic mice with an AD-like pathology harboring human transgenes that cause both age-dependent beta-amyloidosis and tauopathy, whereas Tg2576 mice, which display beta-amyloidosis only, had unchanged PSCA levels compared to wild-type animals. These findings identify PSCA as a nAChR-binding protein in the human brain that is affected in AD, suggesting that PSCA-nAChR interactions may be involved in the cognitive dysfunction observed in AD. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:1629 / 1638
页数:10
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