Evidence map›Paper›PMID 33765007›Full record

ArticlePLoS computational biology2021

Analysis of spiking synchrony in visual cortex reveals distinct types of top-down modulation signals for spatial and object-based attention.

Nobuhiko Wagatsuma, Brian Hu, Rüdiger von der Heydt, Ernst Niebur

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 29% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 13 citations in OpenAlex.

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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

4 authors at 2 institutions in 2 countries.

Nobuhiko WagatsumaFaculty of Science, Toho University, Funabashi, Chiba, Japan.ORCID 0000-0001-9090-9223
Brian HuAllen Institute for Brain Science, Seattle, Washington, United States of America.ORCID 0000-0002-5866-8762
Rüdiger von der HeydtZanvyl Krieger Mind/Brain Institute, and Solomon Snyder Department of Neuroscience, Johns Hopkins University, Baltimore, Maryland, United States of America.
Ernst NieburZanvyl Krieger Mind/Brain Institute, and Solomon Snyder Department of Neuroscience, Johns Hopkins University, Baltimore, Maryland, United States of America.ORCID 0000-0002-2815-9262
Allen Institute for Brain Science · USToho University · JP

Funding

CRCNS: Neural decision mechanisms: from value-encoding to preference reversalR01DA040990 · NIDA · JOHNS HOPKINS UNIVERSITY · PI NIEBUR, ERNST, STUPHORN, VEIT · 2015 to 2018
$1.1M
CRCNS:Proto-object based perceptual organization in three dimensionsR01EY027544 · NEI · JOHNS HOPKINS UNIVERSITY · PI ETIENNE-CUMMINGS, RALPH, NIEBUR, ERNST · 2016 to 2018
$1.1M
NEI NIH HHS R01 EY027544NIDA NIH HHS R01 DA040990
6 · The paper itself

Abstract

The activity of a border ownership selective (BOS) neuron indicates where a foreground object is located relative to its (classical) receptive field (RF). A population of BOS neurons thus provides an important component of perceptual grouping, the organization of the visual scene into objects. In previous theoretical work, it has been suggested that this grouping mechanism is implemented by a population of dedicated grouping ("G") cells that integrate the activity of the distributed feature cells representing an object and, by feedback, modulate the same cells, thus making them border ownership selective. The feedback modulation by G cells is thought to also provide the mechanism for object-based attention. A recent modeling study showed that modulatory common feedback, implemented by synapses with N-methyl-D-aspartate (NMDA)-type glutamate receptors, accounts for the experimentally observed synchrony in spike trains of BOS neurons and the shape of cross-correlations between them, including its dependence on the attentional state. However, that study was limited to pairs of BOS neurons with consistent border ownership preferences, defined as two neurons tuned to respond to the same visual object, in which attention decreases synchrony. But attention has also been shown to increase synchrony in neurons with inconsistent border ownership selectivity. Here we extend the computational model from the previous study to fully understand these effects of attention. We postulate the existence of a second type of G-cell that represents spatial attention by modulating the activity of all BOS cells in a spatially defined area. Simulations of this model show that a combination of spatial and object-based mechanisms fully accounts for the observed pattern of synchrony between BOS neurons. Our results suggest that modulatory feedback from G-cells may underlie both spatial and object-based attention.

Indexed as

Models, NeurologicalVisual CortexAction PotentialsAnimalsAttentionComputational BiologyHaplorhiniHumansNeurons

Identifiers

PMID33765007
PMCPMC8023487
OpenAlexW3138662530

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.