4.5 Article

Accurate Localization of Linear Probe Electrode Arrays across Multiple Brains

期刊

ENEURO
卷 8, 期 6, 页码 -

出版社

SOC NEUROSCIENCE
DOI: 10.1523/ENEURO.0241-21.2021

关键词

electrode localization; lightsheet imaging; Neuropixels probes; serial blockface 2P imaging

资金

  1. Howard Hughes Medical Institute
  2. Simons Foundation
  3. Wellcome Trust
  4. Janelia Visiting Scientist Program
  5. Canadian Institutes of Health Research Postdoctoral Fellowship
  6. Sir Henry Wellcome Postdoctoral Fellowship
  7. National Institutes of Health [NS112312]
  8. Robert and Janice McNair Foundation
  9. Searle Scholars Program
  10. Pew Charitable Trusts

向作者/读者索取更多资源

This study evaluates two typical workflows for localizing individual electrodes in standardized brain coordinates, both relying on imaging brains with fluorescent probe tracks and warping 3D image stacks to standardized brain atlases. Groundtruth experiments demonstrate that electrode localization accuracy for recordings from brain regions targeted by the motor cortex is better than 0.1 mm, independent of workflow used.
Recently developed probes for extracellular electrophysiological recordings have large numbers of electrodes on long linear shanks. Linear electrode arrays, such as Neuropixels probes, have hundreds of recording electrodes distributed over linear shanks that span several millimeters. Because of the length of the probes, linear probe recordings in rodents usually cover multiple brain areas. Typical studies collate recordings across several recording sessions and animals. Neurons recorded in different sessions and animals thus have to be aligned to each other and to a standardized brain coordinate system. Here, we evaluate two typical workflows for localization of individual electrodes in standardized coordinates. These workflows rely on imaging brains with fluorescent probe tracks and warping 3D image stacks to standardized brain atlases. One workflow is based on tissue clearing and selective plane illumination microscopy (SPIM), whereas the other workflow is based on serial block-face two-photon (SBF2P) microscopy. In both cases electrophysiological features are then used to anchor particular electrodes along the reconstructed tracks to specific locations in the brain atlas and therefore to specific brain structures. We performed groundtruth experiments, in which motor cortex outputs are labeled with ChR2 and a fluorescence protein. Light-evoked electrical activity and fluorescence can be independently localized. Recordings from brain regions targeted by the motor cortex reveal better than 0.1-mm accuracy for electrode localization, independent of workflow used.

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