A DR6/p75NTR complex is responsible for β-amyloid-induced cortical neuron death

被引:44
|
作者
Hu, Y. [1 ]
Lee, X. [1 ]
Shao, Z. [1 ]
Apicco, D. [1 ]
Huang, G. [1 ]
Gong, B. J. [1 ]
Pepinsky, R. B. [1 ]
Mi, S. [1 ]
机构
[1] Biogen Idec Inc, Dept Discovery Neurobiol, Cambridge, MA 02142 USA
来源
CELL DEATH & DISEASE | 2013年 / 4卷
关键词
DR6; p75(NTR); A beta; AD; neurodegenerative disease; neuronal cell death; P75 NEUROTROPHIN RECEPTOR; ALZHEIMERS-DISEASE; PRO-NGF; P75(NTR); EXPRESSION; APOPTOSIS; PROTEIN; SYSTEM; CASPASES; TARGETS;
D O I
10.1038/cddis.2013.110
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The p75 neurotrophin receptor (p75(NTR)) is a known mediator of beta-amyloid (A beta)-induced neurotoxicity implicated in Alzheimer's disease (AD). Here, we demonstrate that death receptor 6 (DR6) binds to p75(NTR) and is a component of the p75(NTR) signaling complex responsible for A beta-induced cortical neuron death. Cortical neurons isolated from either DR6 or p75(NTR) null mice are resistant to A beta-induced neurotoxicity. Blocking DR6 function in cortical neurons by anti-DR6 antibodies that block the binding of DR6 to p75(NTR) receptor complex or by a dominant negative DR6 construct lacking the cytoplasmic signaling death domain attenuates A beta-induced caspase 3 activation and cell death. DR6 expression is upregulated in AD cortex and correlates with elevated neuronal death. Targeting the disruption of the DR6/p75(NTR) complex to prevent A beta cytotoxicity represents a new approach for the treatment of neurodegenerative disorders such as AD. Cell Death and Disease (2013) 4, e579; doi:10.1038/cddis.2013.110; published online 4 April 2013
引用
收藏
页码:e579 / e579
页数:8
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