Novel technologies for nontoxic transsynaptic tracing

无毒跨突触追踪新技术

• 批准号: 8935945
• 负责人: IAN R WICKERSHAM
• 金额: $ 70.82万
• 依托单位: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-09-26 至 2017-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8935945
• 关键词: Acute; Address; Alzheimer' s Disease; Animals; Area; Behavior; Behavioral; Behavioral Paradigm; Brain; Cognition; Cognitive; Complex; Engineering; Epilepsy; Flow Cytometry; Gene Expression; Gene Expression Profile; Generations; Genes; Genetic; Health; Huntington Disease; Image; In Situ; Individual; Infection; Label; Left; Lentivirus Vector; Mental disorders; Modeling; Monitor; Mus; Neurons; Neurosciences; Parkinson Disease; Physiological; Population; Presynaptic Terminals; Primates; Problem Solving; Rabies; Rabies virus; Rattus; Reporter; Research Personnel; Resolution; Rodent; Role; Slice; Synapses; System; Techniques; Technology; Testing; Time; Toxic effect; Transgenes; Transgenic Organisms; Viral; Viral Genes; Viral Genome; Viral Vector; Virus; Whole-Cell Recordings; autism spectrum disorder; base; calcium indicator; env Gene Products; genetic technology; in vivo; killings; mutant; nervous system disorder; neural circuit; new technology; novel; operation; optical imaging; optogenetics; particle; recombinase; relating to nervous system; research study; tool; transgene expression; vector; virus envelope

 DESCRIPTION (provided by applicant): Genetic tools have dramatically increased the power and resolution of neuroscientific experiments, allowing monitoring and perturbation of specific neuronal populations within the brain, often in the context of complex cognitive and behavioral paradigms. However, the usefulness of these tools is limited by the available means of delivering them in circuit-specific ways, a major drawback in view of the critical importance of specific connectivity between individual neurons and between neuronal classes. The primary available means of achieving transgene expression based on neurons' synaptic connections is virus-based transsynaptic tracing, which allows identification, activity imaging, optogenetic control, and perturbation of gene expression in networks of synaptically connected neurons in vivo. The required viruses, however, are toxic within a few days, precluding longer-term experiments that are needed to address many central questions in neuroscience. We will solve this problem by engineering viral transsynaptic tracing systems with either greatly reduced or entirely eliminated toxicity, so that the role of neuronal networks of known connectivity in cognition and behavior. The result will be a set of tools that will allow optical imaging, physiological recording, and manipulation of the activity and gene expression of neuronal networks of known synaptic connectivity in the context of behavioral and other experimental paradigms lasting weeks, months, or years, in any mammalian model species. This will greatly enhance our understanding of the neural bases of normal cognition as well as neurological and mental disorders.

 描述(申请人提供)：遗传工具极大地提高了神经科学实验的能力和分辨率，允许监测和干扰大脑中的特定神经元群体，通常是在复杂的认知和行为范例的背景下。然而，这些工具的用途受到以特定于电路的方式提供它们的现有手段的限制，鉴于单个神经元之间和神经元类别之间的特定连接的关键重要性，这是一个重大缺陷。基于神经元突触连接实现转基因表达的主要有效手段是基于病毒的跨突触示踪，它可以在体内识别、活动成像、光遗传控制和干扰突触连接神经元网络中的基因表达。然而，所需的病毒在几天内就会中毒，从而排除了解决神经科学中许多核心问题所需的长期实验。我们将通过设计毒性大大降低或完全消除的病毒跨突触追踪系统来解决这个问题，以便已知连接的神经元网络在认知和行为中的作用。其结果将是一套工具，可以在任何哺乳动物模式物种中，在持续数周、数月或数年的行为和其他实验范式的背景下，对已知突触连接的神经元网络的活动和基因表达进行光学成像、生理记录和操纵。这将极大地增强我们对正常认知以及神经和精神障碍的神经基础的理解。