Mechanisms of prion spread

朊病毒传播机制

基本信息

批准号：
8696897
负责人：
Christina Sigurdson
金额：
$ 33.57万
依托单位：
UNIVERSITY OF CALIFORNIA, SAN DIEGO
依托单位国家：
美国
项目类别：
财政年份：
2012
资助国家：
美国
起止时间：
2012-09-15 至 2017-07-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8696897
关键词：
Address Affect Amino Acid Sequence Amyloid beta-Protein Animals Applications Grants Autopsy Axon Axonal Transport Biological Assay Blood Brain Brain region Cessation of life Chronic Wasting Disease Communicable Diseases Deer Deterioration Development Diagnostic Disease Disease Progression Epitopes Experimental Models Exposure to GPI Membrane Anchors Goals Human Immunotherapy In Vitro Infection Infectious Agent Invaded Lead Liquid substance Lymphoid Tissue Maps Measures Membrane Modeling Molecular Molecular Conformation Molecular Structure Mus Nerve Nervous system structure Neuraxis Neurodegenerative Disorders Neurons Pathogenesis Peptide Sequence Determination Peripheral Peripheral Nerves Polymers Population PrPSc Proteins Presynaptic Terminals Prevention Prion Diseases Prions Process Property Publishing Risk Role Science Site Testing Tissues Transfusion Transgenic Mice Virulent biophysical properties exposed human population foodborne in vivo insight neuronal cell body novel therapeutics prevent prion-based protein aggregate protein misfolding retrograde transport screening synuclein tau Proteins therapy development transmission process uptake

项目摘要

DESCRIPTION (provided by applicant): Prion diseases are fatal neurodegenerative disorders caused by an aggregated form of the prion protein, PrPSc. Prions are the only protein aggregates that are naturally transmitted as an infectious disease, and most recently, human to human transmission likely occurred by transfusion of prion-contaminated blood. Most cases of natural transmission occur through a peripheral exposure followed by prion spread to the CNS. Although prions are thought to spread via peripheral nerves to the CNS, the molecular mechanisms underlying neuronal transit are unclear. For this reason, a major goal of this grant application is to understand how prion aggregates spread to the CNS. We hypothesize that prions propagate by retrograde axonal transport and will address this hypothesis using in vitro and in vivo experimental models. To accomplish this goal, three aims are proposed. In the first aim, we will test the mechanism of PrPSc axonal transport using compartmentalized neuronal cultures that have a liquid separation between the axon terminals and the cell bodies. We will additionally assess the peripheral nerve transport of prion strains in vivo. In the second aim, we will measure the structural properties of the highly virulent prion strains that readily spread to he CNS. In the third aim, we will determine the role of the GPI membrane anchor of PrPC on prion spread to the brain using transgenic mice and primary neurons that express PrPC possessing or lacking the GPI anchor. We expect that these studies will provide critical missing information on the basic mechanisms of prion spread that will be essential for the development of immunotherapies and novel therapeutic strategies to prevent or arrest disease progression.

描述（由申请人提供）：朊病毒病是由朊病毒蛋白 PrPSc 的聚集形式引起的致命性神经退行性疾病。朊病毒是唯一一种作为传染病自然传播的蛋白质聚集体，最近，人与人之间的传播可能是通过输注被朊病毒污染的血液而发生的。大多数自然传播病例是通过外周暴露发生的，然后朊病毒传播到中枢神经系统。尽管朊病毒被认为通过周围神经传播到中枢神经系统，但神经元转运的分子机制尚不清楚。因此，本次拨款申请的主要目标是了解朊病毒聚集体如何传播到中枢神经系统。我们假设朊病毒通过逆行轴突运输传播，并将使用体外和体内实验模型来解决这一假设。为了实现这一目标，提出了三个目标。第一个目标是，我们将使用轴突末端和细胞体之间有液体分离的区室化神经元培养物来测试 PrPSc 轴突运输的机制。我们还将评估体内朊病毒株的周围神经转运。在第二个目标中，我们将测量容易传播到中枢神经系统的高毒力朊病毒菌株的结构特性。在第三个目标中，我们将使用转基因小鼠和表达具有或缺乏 GPI 锚的 PrPC 的原代神经元来确定 PrPC 的 GPI 膜锚对朊病毒扩散到大脑的作用。我们期望这些研究将提供有关朊病毒传播基本机制的关键缺失信息，这对于开发免疫疗法和预防或阻止疾病进展的新治疗策略至关重要。