Institute of Biomedical Engineering, Imperial College, London, UK. Devision of Neuroscience, Imperial College, London, UK.
J Neural Eng. 2010 Feb;7(1):16004. doi: 10.1088/1741-2560/7/1/016004. Epub 2010 Jan 14.
Studying neuronal processes such as synaptic summation, dendritic physiology and neural network dynamics requires complex spatiotemporal control over neuronal activities. The recent development of neural photosensitization tools, such as channelrhodopsin-2 (ChR2), offers new opportunities for non-invasive, flexible and cell-specific neuronal stimulation. Previously, complex spatiotemporal control of photosensitized neurons has been limited by the lack of appropriate optical devices which can provide 2D stimulation with sufficient irradiance. Here we present a simple and powerful solution that is based on an array of high-power micro light-emitting diodes (micro-LEDs) that can generate arbitrary optical excitation patterns on a neuronal sample with micrometre and millisecond resolution. We first describe the design and fabrication of the system and characterize its capabilities. We then demonstrate its capacity to elicit precise electrophysiological responses in cultured and slice neurons expressing ChR2.
研究神经元过程,如突触总和、树突生理学和神经网络动力学,需要对神经元活动进行复杂的时空控制。神经光遗传学工具的最新发展,如通道视紫红质-2(ChR2),为非侵入性、灵活和细胞特异性的神经元刺激提供了新的机会。以前,由于缺乏适当的光学器件,无法提供具有足够辐照度的 2D 刺激,因此对光敏感神经元的复杂时空控制受到限制。在这里,我们提出了一种简单而强大的解决方案,该方案基于高功率微发光二极管(micro-LED)阵列,该阵列可以以微米和毫秒分辨率在神经元样本上生成任意光学激发模式。我们首先描述了系统的设计和制造,并对其功能进行了表征。然后,我们证明了它能够在表达 ChR2 的培养和切片神经元中引发精确的电生理反应。