Zyxin is a novel target for beta-amyloid peptide: characterization of its role in Alzheimer's pathogenesis

被引:20
作者
Lanni, Cristina [1 ]
Necchi, Daniela [1 ]
Pinto, Antonella [1 ]
Buoso, Erica [1 ]
Buizza, Laura [2 ]
Memo, Maurizio [2 ]
Uberti, Daniela [2 ]
Govoni, Stefano [1 ]
Racchi, Marco [1 ]
机构
[1] Univ Pavia, Dept Drug Sci, Ctr Excellence Appl Biol, I-27100 Pavia, Italy
[2] Univ Brescia, Dept Biomed Sci & Biotechnol, Brescia, Italy
关键词
Alzheimer's disease; beta-amyloid peptides; conformationally altered p53; metallothionein; 2A; zyxin; PRECURSOR PROTEIN; CELL-DEATH; P53; DISEASE; ACCUMULATION; FIBROBLASTS; STRATEGIES; APOPTOSIS; CANCER; CYCLE;
D O I
10.1111/jnc.12154
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
Zyxin is an adaptor protein recently identified as a novel regulator of the homeodomain-interacting protein kinase 2 (HIPK2)-p53 signaling in response to DNA damage. We recently reported an altered conformational state of p53 in tissues from patients with Alzheimer s disease (AD), because of a deregulation of HIPK2 activity, leading to an impaired and dysfunctional response to stressors. Here, we examined the molecular mechanisms underlying the deregulation of HIPK2 activity in two cellular models, HEK-293 cells and SH-SY5Y neuroblastoma cells differentiated with retinoic acid over-expressing the amyloid precursor protein, focusing on the evidence that zyxin expression is important to maintain HIPK2 protein stability. We demonstrated that both beta-amyloid (A) 1-40 and 1-42 induce zyxin deregulation, thus affecting the transcriptional repressor activity of HIPK2 onto its target promoter, metallothionein 2A, which is in turn responsible for the induction of an altered conformational state of p53. We demonstrate for the first time that zyxin is a novel target of A activities in AD. These results may help the studies on the pathogenesis of AD, through the fine dissection of events related to beta-amyloid activities.
引用
收藏
页码:790 / 799
页数:10
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