Miles R Bryan Iii, Xu Tian, Jui-Heng Tseng, Baggio A Evangelista, Joey V Ragusa, Audra F Bryan, Winifred Trotman, David Irwin, Todd J Cohen
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引用次数: 0
摘要
包括阿尔茨海默病(AD)在内的牛头蛋白病是一类神经退行性疾病,其特征是存在不溶性牛头蛋白包涵体。传统上认为,tau 磷酸化是控制tau功能和tau病发病机制的主要翻译后修饰(PTM)。然而,我们和其他人已经发现,tau乙酰化是一种主要的PTM,它既能调节正常的tau功能,也能调节包括聚集在内的异常致病特征。之前的工作显示,与非tauopathy对照组相比,tauopathy脑(包括AD)中位于tau第二和第三重复区(残基K280和K311)的聚集热点存在强tau乙酰化。通过筛选数千个杂交瘤克隆,我们产生了靶向残基K280或K311乙酰化tau的位点特异性和修饰特异性单克隆抗体。为了在真正的神经元系统中验证这些抗体,我们将乙酰化转移酶CBP靶向到神经元的细胞质中,以促进tau乙酰化。几个抗体克隆特异性地检测到了神经元中CBP乙酰化的tau并与ac-tau共定位。此外,我们的先导优选抗乙酰化 tau 单克隆抗体在人类 AD 大脑的缠结和神经斑块中检测到了强大的 tau 病理学。乙酰化 tau 是 tau 功能的关键调节因子,鉴于人们现在对乙酰化 tau 的兴趣日渐浓厚,这些灵敏度高、特异性强的工具将使我们能够进一步揭开 tau PTM 的密码,重要的是,它们还可以用作诊断或改变疾病的药物。
Development and characterization of novel anti-acetylated tau monoclonal antibodies to probe pathogenic tau species in Alzheimer's disease.
Tauopathies, including Alzheimer's disease (AD), are a class of neurodegenerative diseases characterized by the presence of insoluble tau inclusions. Tau phosphorylation has traditionally been viewed as the dominant post-translational modification (PTM) controlling tau function and pathogenesis in tauopathies. However, we and others have identified tau acetylation as a primary PTM regulating both normal tau function as well as abnormal pathogenic features including aggregation. Prior work showed robust tau acetylation in aggregation hotspots located within the 2nd and 3rd repeat regions of tau (residues K280 and K311) in tauopathy brains, including AD, compared to non-tauopathy controls. By screening thousands of hybridoma clones, we generated site-specific and modification-specific monoclonal antibodies targeting acetylated tau at residues K280 or K311. To validate these antibodies in a bona fide neuronal system, we targeted the acetyltransferase CBP to the cytoplasm of neurons to promote tau acetylation. Several antibody clones specifically detected CBP-acetylated tau and co-localized with ac-tau in neurons. Additionally, our lead optimal anti-acetylated-tau monoclonal antibodies detected robust tau pathology in tangles and neuritic plaques of human AD brains. Given the now emerging interest in acetylated tau as critical regulator of tau functions, these sensitive and highly specific tools will allow us to further unravel the tau PTM code and, importantly, could be deployed as diagnostic or disease-modifying agents.
期刊介绍:
"Acta Neuropathologica Communications (ANC)" is a peer-reviewed journal that specializes in the rapid publication of research articles focused on the mechanisms underlying neurological diseases. The journal emphasizes the use of molecular, cellular, and morphological techniques applied to experimental or human tissues to investigate the pathogenesis of neurological disorders.
ANC is committed to a fast-track publication process, aiming to publish accepted manuscripts within two months of submission. This expedited timeline is designed to ensure that the latest findings in neuroscience and pathology are disseminated quickly to the scientific community, fostering rapid advancements in the field of neurology and neuroscience. The journal's focus on cutting-edge research and its swift publication schedule make it a valuable resource for researchers, clinicians, and other professionals interested in the study and treatment of neurological conditions.