Maccione Alessandro, Gandolfo Mauro, Zordan Stefano, Amin Hayder, Di Marco Stefano, Nieus Thierry, Angotzi Gian Nicola, Berdondini Luca
NetS3 Laboratory, Neuroscience and Brain Technologies, Fondazione Istituto Italiano di Tecnologia, Genova, Italy.
3Brain GmbH, Landquart, Switzerland.
Brain Res Bull. 2015 Oct;119(Pt B):118-26. doi: 10.1016/j.brainresbull.2015.07.008. Epub 2015 Jul 29.
Deciphering neural network function in health and disease requires recording from many active neurons simultaneously. Developing approaches to increase their numbers is a major neurotechnological challenge. Parallel to recent advances in optical Ca(2+) imaging, an emerging approach consists in adopting complementary-metal-oxide-semiconductor (CMOS) technology to realize MultiElectrode Array (MEA) devices. By implementing signal conditioning and multiplexing circuits, these devices allow nowadays to record from several thousands of single neurons at sub-millisecond temporal resolution. At the same time, these recordings generate very large data streams which become challenging to analyze. Here, at first we shortly review the major approaches developed for data management and analysis for conventional, low-resolution MEAs. We highlight how conventional computational tools cannot be easily up-scaled to very large electrode array recordings, and custom bioinformatics tools are an emerging need in this field. We then introduce a novel approach adapted for the acquisition, compression and analysis of extracellular signals acquired simultaneously from 4096 electrodes with CMOS MEAs. Finally, as a case study, we describe how this novel large scale recording platform was used to record and analyze extracellular spikes from the ganglion cell layer in the wholemount retina at pan-retinal scale following patterned light stimulation.
解读健康与疾病状态下神经网络的功能需要同时记录多个活跃神经元。开发增加记录神经元数量的方法是一项重大的神经技术挑战。与光学钙离子成像技术的最新进展并行,一种新兴方法是采用互补金属氧化物半导体(CMOS)技术来实现多电极阵列(MEA)设备。通过集成信号调节和多路复用电路,如今这些设备能够以亚毫秒级的时间分辨率记录数千个单个神经元的活动。与此同时,这些记录产生了非常庞大的数据流,分析起来颇具挑战性。在此,首先我们简要回顾一下为传统低分辨率MEA数据管理和分析所开发的主要方法。我们强调传统计算工具难以轻松扩展用于处理非常大的电极阵列记录,因此该领域迫切需要定制的生物信息学工具。然后,我们介绍一种适用于通过CMOS MEA从4096个电极同时采集、压缩和分析细胞外信号的新方法。最后,作为一个案例研究,我们描述了如何利用这个新型大规模记录平台,在图案化光刺激后,在全视网膜尺度上记录和分析来自整个视网膜神经节细胞层的细胞外尖峰信号。