Cellular prion protein is essential for oligomeric amyloid-β-induced neuronal cell death

被引:100
|
作者
Kudo, Wataru [1 ]
Lee, Hyun-Pil [1 ]
Zou, Wen-Quan [1 ,2 ]
Wang, Xinglong [1 ,2 ]
Perry, George [4 ,5 ]
Zhu, Xiongwei [1 ,2 ]
Smith, Mark A. [1 ]
Petersen, Robert B. [1 ,2 ,3 ]
Lee, Hyoung-gon [1 ,2 ]
机构
[1] Case Western Reserve Univ, Dept Pathol, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Neurol, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Dept Neurosci, Cleveland, OH 44106 USA
[4] Univ Texas San Antonio, UTSA Neurosci Inst, San Antonio, TX USA
[5] Univ Texas San Antonio, Dept Biol, San Antonio, TX USA
基金
美国国家卫生研究院;
关键词
ALZHEIMERS-DISEASE; SYNAPTIC PLASTICITY; RECEPTOR; IMPAIRMENT; TOXICITY;
D O I
10.1093/hmg/ddr542
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
In Alzheimer disease (AD), amyloid- (A) oligomer is suggested to play a critical role in imitating neurodegeneration, although its pathogenic mechanism remains to be determined. Recently, the cellular prion protein (PrPC) has been reported to be an essential co-factor in mediating the neurotoxic effect of A oligomer. However, these previous studies focused on the synaptic plasticity in either the presence or the absence of PrPC and no study to date has reported whether PrPC is required for the neuronal cell death, the most critical element of neurodegeneration in AD. Here, we show that Prnp(/) mice are resistant to the neurotoxic effect of A oligomer in vivo and in vitro. Furthermore, application of an anti-PrPC antibody or PrPC peptide prevents A oligomer-induced neurotoxicity. These findings are the first to demonstrate that PrPC is required for A oligomer-induced neuronal cell death, the pathology essential to cognitive loss.
引用
收藏
页码:1138 / 1144
页数:7
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