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Deep learning-based real-time detection of neurons in brain slices for in vitro physiology

A common electrophysiology technique used in neuroscience is patch clamp: a method in which a glass pipette electrode facilitates single cell electrical recordings from neurons. Typically, patch clamp is done manually in which an electrophysiologist views a brain slice under a microscope, visually s...

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Autores principales: Yip, Mighten C., Gonzalez, Mercedes M., Valenta, Christopher R., Rowan, Matthew J. M., Forest, Craig R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7971045/
https://www.ncbi.nlm.nih.gov/pubmed/33727679
http://dx.doi.org/10.1038/s41598-021-85695-4
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author Yip, Mighten C.
Gonzalez, Mercedes M.
Valenta, Christopher R.
Rowan, Matthew J. M.
Forest, Craig R.
author_facet Yip, Mighten C.
Gonzalez, Mercedes M.
Valenta, Christopher R.
Rowan, Matthew J. M.
Forest, Craig R.
author_sort Yip, Mighten C.
collection PubMed
description A common electrophysiology technique used in neuroscience is patch clamp: a method in which a glass pipette electrode facilitates single cell electrical recordings from neurons. Typically, patch clamp is done manually in which an electrophysiologist views a brain slice under a microscope, visually selects a neuron to patch, and moves the pipette into close proximity to the cell to break through and seal its membrane. While recent advances in the field of patch clamping have enabled partial automation, the task of detecting a healthy neuronal soma in acute brain tissue slices is still a critical step that is commonly done manually, often presenting challenges for novices in electrophysiology. To overcome this obstacle and progress towards full automation of patch clamp, we combined the differential interference microscopy optical technique with an object detection-based convolutional neural network (CNN) to detect healthy neurons in acute slice. Utilizing the YOLOv3 convolutional neural network architecture, we achieved a 98% reduction in training times to 18 min, compared to previously published attempts. We also compared networks trained on unaltered and enhanced images, achieving up to 77% and 72% mean average precision, respectively. This novel, deep learning-based method accomplishes automated neuronal detection in brain slice at 18 frames per second with a small data set of 1138 annotated neurons, rapid training time, and high precision. Lastly, we verified the health of the identified neurons with a patch clamp experiment where the average access resistance was 29.25 M[Formula: see text] (n = 9). The addition of this technology during live-cell imaging for patch clamp experiments can not only improve manual patch clamping by reducing the neuroscience expertise required to select healthy cells, but also help achieve full automation of patch clamping by nominating cells without human assistance.
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spelling pubmed-79710452021-03-19 Deep learning-based real-time detection of neurons in brain slices for in vitro physiology Yip, Mighten C. Gonzalez, Mercedes M. Valenta, Christopher R. Rowan, Matthew J. M. Forest, Craig R. Sci Rep Article A common electrophysiology technique used in neuroscience is patch clamp: a method in which a glass pipette electrode facilitates single cell electrical recordings from neurons. Typically, patch clamp is done manually in which an electrophysiologist views a brain slice under a microscope, visually selects a neuron to patch, and moves the pipette into close proximity to the cell to break through and seal its membrane. While recent advances in the field of patch clamping have enabled partial automation, the task of detecting a healthy neuronal soma in acute brain tissue slices is still a critical step that is commonly done manually, often presenting challenges for novices in electrophysiology. To overcome this obstacle and progress towards full automation of patch clamp, we combined the differential interference microscopy optical technique with an object detection-based convolutional neural network (CNN) to detect healthy neurons in acute slice. Utilizing the YOLOv3 convolutional neural network architecture, we achieved a 98% reduction in training times to 18 min, compared to previously published attempts. We also compared networks trained on unaltered and enhanced images, achieving up to 77% and 72% mean average precision, respectively. This novel, deep learning-based method accomplishes automated neuronal detection in brain slice at 18 frames per second with a small data set of 1138 annotated neurons, rapid training time, and high precision. Lastly, we verified the health of the identified neurons with a patch clamp experiment where the average access resistance was 29.25 M[Formula: see text] (n = 9). The addition of this technology during live-cell imaging for patch clamp experiments can not only improve manual patch clamping by reducing the neuroscience expertise required to select healthy cells, but also help achieve full automation of patch clamping by nominating cells without human assistance. Nature Publishing Group UK 2021-03-16 /pmc/articles/PMC7971045/ /pubmed/33727679 http://dx.doi.org/10.1038/s41598-021-85695-4 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yip, Mighten C.
Gonzalez, Mercedes M.
Valenta, Christopher R.
Rowan, Matthew J. M.
Forest, Craig R.
Deep learning-based real-time detection of neurons in brain slices for in vitro physiology
title Deep learning-based real-time detection of neurons in brain slices for in vitro physiology
title_full Deep learning-based real-time detection of neurons in brain slices for in vitro physiology
title_fullStr Deep learning-based real-time detection of neurons in brain slices for in vitro physiology
title_full_unstemmed Deep learning-based real-time detection of neurons in brain slices for in vitro physiology
title_short Deep learning-based real-time detection of neurons in brain slices for in vitro physiology
title_sort deep learning-based real-time detection of neurons in brain slices for in vitro physiology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7971045/
https://www.ncbi.nlm.nih.gov/pubmed/33727679
http://dx.doi.org/10.1038/s41598-021-85695-4
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