Zhiwen Ye, Andrew M Shelton, Jordan R Shaker, Julien Boussard, Jennifer Colonell, Daniel Birman, Sahar Manavi, Susu Chen, Charlie Windolf, Cole Hurwitz, Han Yu, Tomoyuki Namima, Federico Pedraja, Shahaf Weiss, Bogdan C Raducanu, Torbjørn V Ness, Xiaoxuan Jia, Giulia Mastroberardino, L Federico Rossi, Matteo Carandini, Michael Häusser, Gaute T Einevoll, Gilles Laurent, Nathaniel B Sawtell, Wyeth Bair, Anitha Pasupathy, Carolina Mora Lopez, Barundeb Dutta, Liam Paninski, Joshua H Siegle, Christof Koch, Shawn R Olsen, Timothy D Harris, Nicholas A Steinmetz
{"title":"Ultra-high-density Neuropixels probes improve detection and identification in neuronal recordings.","authors":"Zhiwen Ye, Andrew M Shelton, Jordan R Shaker, Julien Boussard, Jennifer Colonell, Daniel Birman, Sahar Manavi, Susu Chen, Charlie Windolf, Cole Hurwitz, Han Yu, Tomoyuki Namima, Federico Pedraja, Shahaf Weiss, Bogdan C Raducanu, Torbjørn V Ness, Xiaoxuan Jia, Giulia Mastroberardino, L Federico Rossi, Matteo Carandini, Michael Häusser, Gaute T Einevoll, Gilles Laurent, Nathaniel B Sawtell, Wyeth Bair, Anitha Pasupathy, Carolina Mora Lopez, Barundeb Dutta, Liam Paninski, Joshua H Siegle, Christof Koch, Shawn R Olsen, Timothy D Harris, Nicholas A Steinmetz","doi":"10.1016/j.neuron.2025.08.030","DOIUrl":null,"url":null,"abstract":"<p><p>To understand the neural basis of behavior, it is essential to sensitively and accurately measure neural activity at single-neuron and single-spike resolution. Extracellular electrophysiology delivers this, but it has biases in the neurons it detects and it imperfectly resolves their action potentials. To minimize these limitations, we developed a silicon probe with much smaller and denser recording sites than previous designs, called Neuropixels Ultra (NP Ultra). Using NP Ultra, neuronal yield in mouse visual cortex recordings increased by more than 2-fold. With ultra-high spatial resolution, we discovered that a feature of extracellular waveforms, the spatial extent or \"footprint,\" distinguished axonal from somatic recordings. In addition, three genetically identified cortical cell types could be discriminated from one another with ∼80% accuracy and from other neurons with ∼85% accuracy. NP Ultra improves yield, detection of subcellular compartments, and cell type identification to enable a more powerful dissection of neural circuit activity during behavior.</p>","PeriodicalId":19313,"journal":{"name":"Neuron","volume":" ","pages":""},"PeriodicalIF":15.0000,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuron","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.neuron.2025.08.030","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
To understand the neural basis of behavior, it is essential to sensitively and accurately measure neural activity at single-neuron and single-spike resolution. Extracellular electrophysiology delivers this, but it has biases in the neurons it detects and it imperfectly resolves their action potentials. To minimize these limitations, we developed a silicon probe with much smaller and denser recording sites than previous designs, called Neuropixels Ultra (NP Ultra). Using NP Ultra, neuronal yield in mouse visual cortex recordings increased by more than 2-fold. With ultra-high spatial resolution, we discovered that a feature of extracellular waveforms, the spatial extent or "footprint," distinguished axonal from somatic recordings. In addition, three genetically identified cortical cell types could be discriminated from one another with ∼80% accuracy and from other neurons with ∼85% accuracy. NP Ultra improves yield, detection of subcellular compartments, and cell type identification to enable a more powerful dissection of neural circuit activity during behavior.
期刊介绍:
Established as a highly influential journal in neuroscience, Neuron is widely relied upon in the field. The editors adopt interdisciplinary strategies, integrating biophysical, cellular, developmental, and molecular approaches alongside a systems approach to sensory, motor, and higher-order cognitive functions. Serving as a premier intellectual forum, Neuron holds a prominent position in the entire neuroscience community.