Targeting Prion-like Cis Phosphorylated Tau Pathology in Neurodegenerative Diseases.

Onder Albayram, Peter Angeli, Elizabeth Bernstein, Sean Baxley, Ziang Gao, Kun Ping Lu, Xiao Zhen Zhou
{"title":"Targeting Prion-like Cis Phosphorylated Tau Pathology in Neurodegenerative Diseases.","authors":"Onder Albayram,&nbsp;Peter Angeli,&nbsp;Elizabeth Bernstein,&nbsp;Sean Baxley,&nbsp;Ziang Gao,&nbsp;Kun Ping Lu,&nbsp;Xiao Zhen Zhou","doi":"10.4172/2161-0460.1000443","DOIUrl":null,"url":null,"abstract":"<p><p>Tau is a microtubule-associated protein heavily implicated in neurodegenerative diseases collectively known as tauopathies, including Alzheimer's disease and chronic traumatic encephalopathy. Phosphorylation of tau at Thr231 allows for the isomerization of phosphorylated tau (p-tau) into distinct cis and trans conformations. Cis, but not trans, p-tau is detectable not only in Alzheimer's disease and chronic traumatic encephalopathy, but also right after traumatic brain injury depending on injury severity and frequency both in humans and animal models. Cis p-tau is not only neurotoxic but also spreads from a neuron to another in a prion-like fashion, functioning as a primary driver of neurodegeneration, which can be effectively neutralized by cis p-tau antibody. This represents an exciting new opportunity for understanding disease development and developing early biomarkers and effective therapies of tauopathies.</p>","PeriodicalId":15013,"journal":{"name":"Journal of Alzheimer's disease & Parkinsonism","volume":"8 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4172/2161-0460.1000443","citationCount":"13","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Alzheimer's disease & Parkinsonism","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/2161-0460.1000443","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2018/6/29 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 13

Abstract

Tau is a microtubule-associated protein heavily implicated in neurodegenerative diseases collectively known as tauopathies, including Alzheimer's disease and chronic traumatic encephalopathy. Phosphorylation of tau at Thr231 allows for the isomerization of phosphorylated tau (p-tau) into distinct cis and trans conformations. Cis, but not trans, p-tau is detectable not only in Alzheimer's disease and chronic traumatic encephalopathy, but also right after traumatic brain injury depending on injury severity and frequency both in humans and animal models. Cis p-tau is not only neurotoxic but also spreads from a neuron to another in a prion-like fashion, functioning as a primary driver of neurodegeneration, which can be effectively neutralized by cis p-tau antibody. This represents an exciting new opportunity for understanding disease development and developing early biomarkers and effective therapies of tauopathies.

Abstract Image

Abstract Image

神经退行性疾病中靶向朊病毒样顺式磷酸化Tau病理学。
Tau是一种微管相关蛋白,与神经退行性疾病(统称为Tau病)密切相关,包括阿尔茨海默病和慢性创伤性脑病。在Thr231处的tau磷酸化允许磷酸化的tau(p-tau)异构化为不同的顺式和反式构象。顺式(而非反式)p-tau不仅在阿尔茨海默病和慢性创伤性脑病中可检测到,而且在创伤性脑损伤后也可检测到——这取决于人类和动物模型中损伤的严重程度和频率。顺式对tau不仅具有神经毒性,而且以朊病毒样的方式从一个神经元传播到另一个神经元,是神经退行性变的主要驱动因素,可以被顺式对tau抗体有效中和。这代表了一个令人兴奋的新机会,可以了解疾病的发展,开发早期的生物标志物和taopathies的有效疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信