Evidence map›Paper›PMID 40794794›Full record

ArticlePLoS computational biology2025

Near-random connections support top-down feature-based attentional modulations in early sensory cortex.

Sunyoung Park, John T Serences

Abstract read
In one paragraph

Article in PLoS computational biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Distributed and drifting signals for working memory load in human cortex.bioRxiv : the preprint server for biology · 2025
    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.

Sunyoung ParkDepartment of Psychology, University of California, San Diego, La Jolla, California, United States of America.ORCID 0000-0002-7994-560X
John T SerencesDepartment of Psychology, University of California, San Diego, La Jolla, California, United States of America.ORCID 0000-0002-8551-5147

Funding

Adaptive population codes for flexible visually-guided behaviorsR01EY025872 · NEI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI John T Serences · 2016 to 2026
$4.5M
NEI NIH HHS R01 EY025872
6 · The paper itself

Abstract

Top-down feedback from prefrontal cortex (PFC) can enhance the gain of feature selective neurons in early sensory areas that are tuned to behaviorally relevant stimuli (termed feature-based attention). Importantly, feature-based attention can even modulate the gain of neurons that do not respond directly to the spatial location of the relevant stimulus, a phenomenon that is thought to globally prime sensitivity to detect relevant features - irrespective of their location - during visual search. However, the neurons in PFC that are thought to provide top-down feedback typically have high-dimensional tuning for multiple features, so it is unclear how feedback selectively modulates responses in neurons tuned to a relevant stimulus without incidentally causing interference by co-modulating neurons tuned to irrelevant features. To investigate this issue, we adapted a spiking neural network model with a first 'sensory' layer composed of neurons selective for single features. Neurons in a second 'control' layer formed random and reciprocal connections with different sensory neurons, giving rise to PFC-like high-dimensional feature tuning. Stimulating second layer neurons that responded robustly to a relevant stimulus led to corresponding gain modulations in sensory neurons that were directly driven by a relevant stimulus. Importantly, no spurious stimulus-like representations arose in unstimulated sensory neurons - despite high-dimensional tuning in second layer neurons - because the random connections averaged out feedback targeted on irrelevant features. Next, we show that subtly increasing the probability that similarly tuned sensory neurons converge on the same second layer neurons can yield most of the noise-cancelling benefits of completely random connections while simultaneously producing spatially global feature-selective modulations in unstimulated sensory neurons. Collectively, these results suggest that a delicate balance between randomness and structure can support top-down feedback signals that globally enhance sensory neurons tuned to relevant features, without leading to spurious stimulus representations that might interfere with perceptual processing.

Indexed as

AttentionModels, NeurologicalAction PotentialsAnimalsComputational BiologyHumansNerve NetNeural Networks, ComputerNeuronsPrefrontal CortexSensory Receptor Cells

Identifiers

PMID40794794
PMCPMC12364372

What OpenQuestion holds

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Registered trials

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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.