Microfluidic Systems to Address Networks of Neurons

用于处理神经元网络的微流体系统

• 批准号: 7432585
• 负责人: ANDREW G EWING
• 金额: $ 29.01万
• 依托单位: PENNSYLVANIA STATE UNIVERSITY, THE
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-06-01 至 2010-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7432585
• 关键词: Address; Affect; Biological Neural Networks; Biology; Brain; Caffeine; Cell Communication; Cells; Chemicals; Chromosome Pairing; Collaborations; Communication; Complex; Cultured Cells; Detection; Development; Dimensions; Dopamine; Dopaminergic Cell; Engineering; Environment; Exposure to; Fluorescence; Fluorescent Probes; Glutamates; Goals; In Vitro; Incubated; Individual; Knowledge; Life; Localized; Methods; Microfluidic Analytical Techniques; Microfluidic Microchips; Microfluidics; Modeling; Monitor; Nanotechnology; Nerve; Neurons; Neuroprotective Agents; Nicotine; Parkinson Disease; Pathway interactions; Pattern; Pharmaceutical Preparations; Play; Preclinical Drug Evaluation; Process; Proteins; Protocols documentation; Rate; Reagent; Recovery; Research; Research Personnel; Role; Screening procedure; Solutions; Synapses; Synaptic Receptors; Synaptic plasticity; System; Techniques; Technology; Testing; Time; Toxin; Trauma; Work; base; cell injury; design; embryonic stem cell; imprint; interest; monitoring device; nanofabrication; nanofluidic; neuron loss; neurotransmission; postsynaptic; programs; receptor; research study; response; success; tool; two-dimensional

DESCRIPTION (provided by applicant): The long term goal of this research is to develop a microfluidic platform to investigate the intercommunication of nerve cells in networks and the influence of the interconnections between cells on the neuronal response to physical trauma and exposure to chemical toxins. A key aspect of this work will be to develop and utilize three-dimensional microfluidic systems to precisely control delivery of reagents to individual cells in a network and to use this system to further our understanding of cell-to-cell communication. Cell networks in vitro will be used to model complex communication in the larger network of the brain. Special emphasis will be placed on understanding pre- vs. postsynaptic receptors, plasticity in patterns and screening for pharmacological efficacy with multiple cells at once. It is normally difficult to carry out detailed studies of drugs, toxins or damage to specific cells in neural networks owing to an inability to simultaneously stimulate (or expose to drug, toxin) and record from several specific cells in an array or network. The system proposed will provide a solution to this problem. We expect the work will expand existing knowledge concerning molecule-based cell-to-cell communication pathways and provide new avenues for screening drugs and toxins involved in the brain. There are four specific aims for this proposal. First, an integrated system will be designed and fabricated to allow linear cell arrays to be non-invasively stimulated and continuously monitored in real-time. Second, a three-dimensional microfluidic device combining small apertures with cross flow will be used to address more complicated two-dimensional cell networks. Third, the microfluidic system combined with fluorescence monitoring of cell activity will be tested on PC12 and P19 cell networks as models. Fourth, neuronal cell cultures with functional synapses will be monitored. The long-term goal is to use this system to examine the effects of physical and chemical damage to specific cells in a neuronal network. We propose to test the hypotheses that 1) neuronal connectivity changes to compensate for neuronal loss following physical damage, 2) activity in neuronal networks affects the rate of degradation following exposure to toxins, 3) glutamate neurons play an active role in dopaminergic neuronal cell loss following exposure toxins, and 4) L-DOPA plays a role in the progression of cell loss in Parkinson's Disease and might be involved in the mechanism of action of neuroprotective agents on dopamine cells. The proposed research has the overarching goal of establishing microfluidics as a valuable tool for biology.

描述（由申请人提供）：本研究的长期目标是开发一种微流体平台，以研究网络中神经细胞的相互通信以及细胞之间的相互连接对神经元对物理创伤和暴露于化学毒素的反应的影响。这项工作的一个关键方面将是开发和利用三维微流体系统来精确控制试剂向网络中单个细胞的递送，并使用该系统来进一步了解细胞间的通信。体外细胞网络将用于模拟大脑更大网络中的复杂通信。特别强调将放在了解前与突触后受体，可塑性的模式和筛选药理学疗效与多个细胞一次。由于不能同时刺激（或暴露于药物、毒素）和记录阵列或网络中的几个特定细胞，通常难以对神经网络中的特定细胞的药物、毒素或损伤进行详细研究。所提出的系统将为这一问题提供解决方案。我们希望这项工作将扩大现有的知识，有关分子为基础的细胞到细胞的通信途径，并提供新的途径，筛选药物和毒素参与大脑。这项建议有四个具体目标。首先，将设计和制造一个集成系统，以允许线性细胞阵列进行非侵入性刺激和实时连续监测。第二，将小孔与交叉流相结合的三维微流体装置将用于处理更复杂的二维细胞网络。第三，将在PC 12和P19细胞网络上作为模型测试与细胞活性的荧光监测相结合的微流体系统。第四，将监测具有功能性突触的神经元细胞培养物。长期目标是使用该系统来检查物理和化学损伤对神经元网络中特定细胞的影响。我们建议测试以下假设：1）神经元连接变化以补偿物理损伤后的神经元损失，2）神经元网络中的活性影响暴露于毒素后的降解速率，3）谷氨酸神经元在暴露于毒素后的多巴胺能神经元细胞损失中起积极作用，4）L-DOPA在帕金森病细胞丢失的进程中起作用，并可能参与神经保护剂对多巴胺细胞的作用机制。这项研究的总体目标是将微流体技术作为一种有价值的生物学工具。