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PseudoSorter: A self-supervised spike sorting approach applied to reveal Tau-induced reductions in neuronal activity.

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Peer-reviewed

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Abstract

Microelectrode arrays (MEAs) permit recordings with high electrode counts, thus generating complex datasets that would benefit from precise neuronal spike sorting for meaningful data extraction. Nevertheless, conventional spike sorting methods face limitations in recognizing diverse spike shapes. Here, we introduce PseudoSorter, which uses self-supervised learning techniques, a density-based pseudolabeling strategy, and an iterative fine-tuning process to enhance spike sorting accuracy. Through benchmarking, we demonstrate the superior performance of PseudoSorter compared to other spike sorting algorithms before applying PseudoSorter on MEA recordings from hippocampal neurons exposed to subneuronal concentrations of monomeric Tau as a model for Alzheimer's disease. Our results unveil that Tau diminishes the firing rate of a subset of neurons, which complement our findings observed using conventional electrophysiology analysis, and demonstrate that PseudoSorter's high accuracy and throughput make it a valuable tool for studying neurodegenerative diseases, enhancing our understanding of their underlying mechanisms, as well as for therapeutic drug screening.

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Journal Title

Sci Adv

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Journal ISSN

2375-2548
2375-2548

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Publisher

American Association for the Advancement of Science (AAAS)

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Except where otherwised noted, this item's license is described as Attribution 4.0 International
Sponsorship
Engineering and Physical Sciences Research Council (EP/H018301/1)
Wellcome Trust (089703/Z/09/Z)
Medical Research Council (MR/K015850/1)
Medical Research Council (MR/K02292X/1)
Engineering and Physical Sciences Research Council (EP/L015889/1)
Wellcome Trust (203249/Z/16/Z)
NFL acknowledges a Career Grant from the Swiss National Science Foundation (P2EZP2_199843). CFK acknowledges funding from the UK Engineering and Physical Science Research Council (EP/L015889/1, EP/H018301/1), the Wellcome Trust (3-3249/Z/16/Z, 089703/Z/09/Z), the UK Medical Research Council (MR/K015850/1, MR/K02292X/1), and Infinitus (China) Company Ltd. GGM acknowledges support from a HORIZON EUROPE UKRI UNDERWRITE INNOVATE grant (COPE-Nano, 10078978). TF and OP acknowledge support from Alzheimer’s Research UK (ARUK-ECRBF2023A-004). GSKS acknowledges funding from the Wellcome Trust (065807/Z/01/Z, 203249/Z/16/Z), the UK Medical Research Council (MR/K02292X/1), Alzheimer’s Research UK (ARUK-PG013-14), the Michael J Fox Foundation (16238, 022159), and Infinitus (China) Company Ltd.

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