Genetically encoded anatomical probes for neuronal activity and plasticity
Genetically encoded anatomical probes for neuronal activity and plasticity
批准号:
7724792
负责人:
Fan Wang
金额:
$31.2万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-07-01 至 2013-05-31
关键词:
AreaCalciumComplexDetectionDevelopmentDiseaseEpilepsyFunctional disorderFutureLabelLearningMemoryMental disordersMolecularNervous System PhysiologyNervous system structureNeurologicNeuronal PlasticityNeuronsNeurosciences ResearchOptical MethodsPerceptionPhysiologyProcessProteinsSensorySynapsesTherapeutic InterventionTranslatingTranslationsWorkaddictionbasechronic paindepressiondesignin vivoneural circuitnovelrelating to nervous systemsensorvoltage
中文摘要
神经科学研究中的一个主要挑战是确定负责各种神经系统过程(如感官知觉,学习和记忆)的精确功能神经回路,以及强调慢性疼痛,抑郁,成瘾和癫痫等病理条件的异常回路。在这一领域以前的工作集中在设计分子传感器,检测瞬态电压变化或钙离子流入使用光学方法。然而,使用这些传感器研究在体内复杂的神经生理学,和哺乳动物神经系统的病理生理学过程已经非常有限。此外,这些传感器不允许激活回路的解剖重建。在尤里卡应用中,我们建议开发新的遗传编码解剖探针,用于直接可视化神经元活动和可塑性。这些探针将用标记物(例如荧光蛋白)标记激活的神经元和突触(以及最可能经历可塑性的那些),以便于组织学检测和解剖学追踪。这种非常规探针设计的主要原理是使用活性(强钙内流)来诱导否则未翻译的标记蛋白的翻译。活动诱导解剖探针的成功开发将极大地促进我们对神经系统功能和功能障碍的理解。
英文摘要
A major challenge in neuroscience research is to identify the precise functional neural circuits that are responsible for diverse nervous system processes such as sensory perception, learning and memory, as well as the aberrant circuits that underline the pathological conditions such as chronic pain, depression, addiction, and epilepsy. Previous work in this area has focused on designing molecular sensors that detect transient voltage change or calcium influx using optical methods. However, the use of these sensors for studying in vivo complex neural physiology, and pathophysiology processes of the mammalian nervous system have been extremely limited. Moreover, these sensors do not allow for anatomical re-construction of the activated circuits. In this EUREKA application, we propose to develop novel genetically encoded anatomical probes for visualizing neuronal activity and plasticity directly. These probes will label activated neurons and synapses (and those most likely undergo plasticity) with a marker (e.g. a fluorescent protein) for easy histological detection and anatomical tracing. The chief principle underlying this unconventional design of probes is to use activity (strong calcium influx) to induce the translation of an otherwise un-translated marker protein. Successful development of the activity-induced anatomical probes will greatly advance our understanding of the functions and dysfunctions of the nervous system.
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