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Monolithically Integrated mu LEDs on Silicon Neural Probes for High-Resolution Optogenetic Studies in Behaving Animals

机译:硅神经探针上的单片集成mu LED,用于行为动物的高分辨率光遗传学研究

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We report a scalable method to monolithically integrate microscopic light emitting diodes (mu LEDs) and recording sites onto silicon neural probes for optogenetic applications in neuroscience. Each mu LED and recording site has dimensions similar to a pyramidal neuron soma, providing confined emission and electrophysiological recording of action potentials and local field activity. We fabricated and implanted the four-shank probes, each integrated with 12 mu LEDs and 32 recording sites, into the CA1 pyramidal layer of anesthetized and freely moving mice. Spikes were robustly induced by 60 nW light power, and fast population oscillations were induced at the microwatt range. To demonstrate the spatiotemporal precision of parallel stimulation and recording, we achieved independent control of distinct cells similar to 50 mu m apart and of differential somato-dendritic compartments of single neurons. The scalability and spatiotemporal resolution of this monolithic optogenetic tool provides versatility and precision for cellular-level circuit analysis in deep structures of intact, freely moving animals.
机译:我们报告了一种可扩展的方法,用于将微观发光二极管(mu LED)单片集成到硅神经探针上,并将其记录在神经科学中进行光遗传学应用。每个mu LED和记录位点的尺寸都类似于锥体神经元体,提供了动作电位和局部场活动的受限发射和电生理记录。我们将四柄探针(每个探针都集成了12亩LED和32个记录位点)制作并植入到麻醉和自由移动的小鼠的CA1锥体层中。 60 nW的光功率强烈引起尖峰,并在微瓦范围内引起快速的总体振荡。为了证明并行刺激和记录的时空精度,我们实现了对相距50μm的不同细胞以及单个神经元的不同体细胞-树突区室的独立控制。这种整体式光遗传学工具的可扩展性和时空分辨率为完整,自由移动的动物的深层结构中的细胞级电路分析提供了多功能性和精度。

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