Evidence map›Paper›PMID 37279242›Full record

ArticlePLoS computational biology2023

Identifying properties of pattern completion neurons in a computational model of the visual cortex.

Casey M Baker, Yiyang Gong

Abstract read
In one paragraph

Article in PLoS computational biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Casey M BakerDepartment of Biomedical Engineering, Duke University, Durham, North Carolina, United States of America.ORCID 0000-0002-3661-9900
Yiyang GongDepartment of Biomedical Engineering, Duke University, Durham, North Carolina, United States of America.ORCID 0000-0002-1855-930X

Funding

Voltage Imaging Dissection of the Mammalian CortexDP2NS111505 · NINDS · DUKE UNIVERSITY · PI GONG, YIYANG · 2018 to 2018
$2.4M
Large-scale cellular-resolution voltage imaging of the zebrafish brainUF1NS107678 · NINDS · DUKE UNIVERSITY · PI GONG, YIYANG · 2018 to 2018
$1.2M
NINDS NIH HHS DP2 NS111505NINDS NIH HHS UF1 NS107678
6 · The paper itself

Abstract

Neural ensembles are found throughout the brain and are believed to underlie diverse cognitive functions including memory and perception. Methods to activate ensembles precisely, reliably, and quickly are needed to further study the ensembles' role in cognitive processes. Previous work has found that ensembles in layer 2/3 of the visual cortex (V1) exhibited pattern completion properties: ensembles containing tens of neurons were activated by stimulation of just two neurons. However, methods that identify pattern completion neurons are underdeveloped. In this study, we optimized the selection of pattern completion neurons in simulated ensembles. We developed a computational model that replicated the connectivity patterns and electrophysiological properties of layer 2/3 of mouse V1. We identified ensembles of excitatory model neurons using K-means clustering. We then stimulated pairs of neurons in identified ensembles while tracking the activity of the entire ensemble. Our analysis of ensemble activity quantified a neuron pair's power to activate an ensemble using a novel metric called pattern completion capability (PCC) based on the mean pre-stimulation voltage across the ensemble. We found that PCC was directly correlated with multiple graph theory parameters, such as degree and closeness centrality. To improve selection of pattern completion neurons in vivo, we computed a novel latency metric that was correlated with PCC and could potentially be estimated from modern physiological recordings. Lastly, we found that stimulation of five neurons could reliably activate ensembles. These findings can help researchers identify pattern completion neurons to stimulate in vivo during behavioral studies to control ensemble activation.

Indexed as

NeuronsVisual CortexAnimalsMice

Identifiers

PMID37279242
PMCPMC10275485

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.