Investigating Mechanisms of Neurodegeneration in Transgenic Mouse Models of Tauopathies

研究 Tau蛋白病转基因小鼠模型中神经变性的机制

基本信息

批准号：
10617695
负责人：
Yuxing Xia
金额：
$ 2.31万
依托单位：
UNIVERSITY OF FLORIDA
依托单位国家：
美国
项目类别：
财政年份：
2021
资助国家：
美国
起止时间：
2021-03-08 至 2023-05-19
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/10617695
关键词：
3xTg-AD mouse AD transgenic mice Acceleration Affect Age Alzheimer&apos s Disease Alzheimer&apos s disease model Alzheimer&apos s disease patient Animal Model Antibodies Biochemistry Biological Markers Brain Brain region Cell Count Clinical Cognitive deficits Cryoelectron Microscopy Cultured Cells Disease Disease Progression Drug Screening Fellowship Frontotemporal Dementia Genes Goals Golgi Apparatus Hippocampus Histopathology Human Immunotherapy Impaired cognition Longevity Memory Loss Memory impairment Modeling Molecular Monoclonal Antibodies Mosaicism Motor Mus Mutation Nerve Degeneration Neurodegenerative Disorders Neurofibrillary Tangles Neurons Pathogenicity Pathology Persons Phenotype Phosphorylation Pick body Rapid screening Reproducibility Research Proposals Role Severities Stains Structure Symptoms Tauopathies Testing Therapeutic Therapeutic Studies Time Training Transgenic Mice Translational Research behavior test cerebral atrophy clinical predictors disease mechanisms study disease phenotype disease-causing mutation effectiveness testing familial Alzheimer disease hyperphosphorylated tau interdisciplinary approach mouse model neurotoxicity novel novel therapeutics screening tau Proteins tau aggregation tau expression tau mutation tau-1 transmission process uptake

项目摘要

Project Summary/Abstract Alzheimer’s disease (AD) is the most common neurodegenerative disease that affects over 25 million people worldwide. In AD, hyperphosphorylated tau inclusions like neurofibrillary tangles are one of the earliest changes and can predict clinical severity. As tau inclusions increase, cognitive decline and memory loss worsen over time. Since familial and sporadic AD share the same pathology and clinical symptoms, transgenic mice that express human tau can effectively model AD. However, many existing tau mouse models do not develop both cognitive deficits and robust pathology in the cortex and hippocampus, which are the primary regions of neurodegeneration in AD. In the field, there is a compelling need to develop an effective animal model of tauopathies for mechanistic and therapeutic studies. A good model of tauopathies must meet at least four criteria: 1) develops progressive phosphorylated tau inclusions; 2) affects the primary brain regions of cortex and hippocampus like in AD patients; 3) causes cognitive deficits; and 4) is reproducible with stable germline transmission. To meet this demand, my main translational research goal is to develop a robust animal model for 1. studying disease mechanisms of tau aggregation and hyperphosphorylation and for 2. rapid screening of drugs and therapies. Given that mice have much shorter lifespans, expression of a single disease-causing mutation may not be sufficient to induce a robust disease phenotype. In the field of neurodegeneration, multiple pathogenic mutations are commonly used to accelerate disease phenotypes in transgenic mice. For example, 3XTg-AD and 5XFAD mouse models use three and five different mutations of multiple genes respectively. As a result, I chose to enhance tau neurotoxicity by combining two disease-causing mutations (P301S/S320F) in the same gene. For this research proposal, my lab and I used pronuclear integration to generate novel transgenic mice for stable germline expression of the tau mutations P301S/S320F. With this unprecedent mouse model, I will determine the role of tau hyperphosphorylation in promoting tau aggregation, cognitive deficits and brain atrophy in Specific Aims 1 and 2. In Specific Aim 3, I will use this novel mouse model to screen phospho-tau immunotherapies. Upon completion of this study, I will fulfill my fellowship training goals of studying disease mechanisms of tau- induced neurodegeneration and developing novel immunotherapies for the treatment of AD.

项目摘要/摘要阿尔茨海默氏病（AD）是最常见的神经退行性疾病，影响超过2500万人全世界。在AD中，高磷酸化的TAU夹杂物（如神经纤维缠结）是最早的变化之一并可以预测临床严重程度。随着tau夹杂物的增加，随着时间的推移，认知能力下降和记忆力损失越来越糟。由于家庭和零星广告具有相同的病理和临床符号，因此表达的转基因小鼠人tau可以有效地对广告进行建模。但是，许多现有的tau鼠标模型都不发展认知皮质和海马中的缺陷和鲁棒病理学，这是神经退行性的主要区域在广告中。在现场，有迫切需要开发有效的功模的动物模型和治疗研究。良好的auopathies模型必须符合至少四个标准：1）发展进步磷酸化的tau夹杂物； 2）像AD患者一样影响皮质和海马的主要大脑区域； 3）导致认知定义；和4）可以通过稳定的种系传输来重现。为了满足这一需求，我的主要翻译研究目标是为1开发可靠的动物模型。 tau聚集和高磷酸化的疾病机制以及2。疗法。鉴于小鼠的寿命较短，因此表达单个引起疾病的突变的表达可能不足以诱导强大的疾病表型。在神经退行性的领域，多重致病性突变通常用于加速转基因小鼠的疾病表型。例如，3xtg-ad和 5XFAD小鼠模型分别使用三个和五个不同的多个基因突变。结果，我选择了通过在同一基因中结合两个引起疾病的突变（P301S/S320F）来增强TAU神经毒性。对于这项研究建议，我和我的实验室使用前核整合来生成新型的转基因小鼠以稳定 Tau突变P301S/S320F的种系表达。使用这种前所未有的鼠标模型，我将确定 tau高磷酸化在促进tau聚集，认知缺陷和脑萎缩中的作用在特定方面目标1和2。在特定的目标3中，我将使用这种新型的小鼠模型来筛选磷酸-TAU免疫疗法。这项研究完成后，我将实现研究tau-的疾病机制的奖学金培训目标诱导神经变性并开发用于治疗AD的新型免疫疗法。

项目成果

期刊论文数量（10）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

"Don't Phos Over Tau": recent developments in clinical biomarkers and therapies targeting tau phosphorylation in Alzheimer's disease and other tauopathies.

DOI：
10.1186/s13024-021-00460-5
发表时间：
2021-06-05
期刊：
Molecular neurodegeneration
影响因子：
15.1
作者：
Xia Y;Prokop S;Giasson BI
通讯作者：
Giasson BI

Cellular processing of α-synuclein fibrils results in distinct physiological C-terminal truncations with a major cleavage site at residue Glu 114.

DOI：
10.1016/j.jbc.2023.104912
发表时间：
2023-07
期刊：
JOURNAL OF BIOLOGICAL CHEMISTRY
影响因子：
4.8
作者：
Quintin, Stephan;Lloyd, Grace M.;Paterno, Giavanna;Xia, Yuxing;Sorrentino, Zachary;Bell, Brach M.;Gorion, Kimberly-Marie;Lee, Edward B.;Prokop, Stefan;Giasson, Benoit I.
通讯作者：
Giasson, Benoit I.

Pathogenic tau recruits wild-type tau into brain inclusions and induces gut degeneration in transgenic SPAM mice.