Optogenetics has proven to be a revolutionary technology in neuroscience and has advanced continuously over the past decade. However, optical stimulation technologies for in vivo need to be developed to match the advances in genetics and biochemistry that have driven this field. In particular, conventional approaches for in vivo optical illumination have a limitation on the achievable spatio-temporal resolution. Here we utilize a sapphire-based microscale gallium nitride light-emitting diode (µLED) probe to activate neocortical neurons in vivo. The probes were designed to contain independently controllable multiple µLEDs, emitting at 450 nm wavelength with an irradiance of up to 2 W/mm2. Monte-Carlo stimulations predicted that optical stimulation using a µLED can modulate neural activity within a localized region. To validate this prediction, we tested this probe in the mouse neocortex that expressed channelrhodopsin-2 (ChR2) and compared the results with optical stimulation through a fiber at the cortical surface. We confirmed that both approaches reliably induced action potentials in cortical neurons and that the µLED probe evoked strong responses in deep neurons. Due to the possibility to integrate many optical stimulation sites onto a single shank, the µLED probe is thus a promising approach to control neurons locally in vivo.
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机译:事实证明,光遗传学是神经科学领域的一项革命性技术,并且在过去十年中不断发展。但是,需要开发用于体内的光刺激技术,以匹配驱动该领域的遗传学和生物化学技术的进步。特别地,用于体内光学照明的常规方法在可实现的时空分辨率上具有局限性。在这里,我们利用基于蓝宝石的微型氮化镓发光二极管(µLED)探针在体内激活新皮层神经元。探针设计为包含可独立控制的多个µLED,它们以450 nm的波长发射,辐照度最高为2 W / mm2。蒙特卡洛刺激预测,使用µLED进行的光刺激可以调节局部区域内的神经活动。为了验证该预测,我们在小鼠新皮层中测试了该探针,该探针表达Channelrhodopsin-2(ChR2),并将结果与通过皮质表面纤维的光刺激进行了比较。我们证实,这两种方法都能可靠地诱导皮层神经元的动作电位,并且µLED探针在深层神经元中引起强烈的反应。由于可以将许多光刺激部位整合到单个柄上,因此µLED探针是一种在体内局部控制神经元的有前途的方法。
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