A Normalization Circuit Underlying Coding of Spatial Attention in Primate Lateral Prefrontal Cortex.

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A Normalization Circuit Underlying Coding of Spatial Attention in Primate Lateral Prefrontal Cortex. / Duong, Lyndon; Leavitt, Matthew L; Pieper, Florian; Sachs, Adam J.; Martinez-Trujillo, Julio C.

In: ENEURO, Vol. 6, No. 2, 20.04.2019.

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@article{27aedf7a087347a0b4c45b09b228c60b,
title = "A Normalization Circuit Underlying Coding of Spatial Attention in Primate Lateral Prefrontal Cortex.",
abstract = "Lateral prefrontal cortex (LPFC) neurons signal the allocation of voluntary attention; however, the neural computations underlying this function remain unknown. To investigate this, we recorded from neuronal ensembles in the LPFC of two Macaca fascicularis performing a visuospatial attention task. LPFC neural responses to a single stimulus were normalized when additional stimuli/distracters appeared across the visual field and were well-characterized by an averaging computation. Deploying attention toward an individual stimulus surrounded by distracters shifted neural activity from an averaging regime toward a regime similar to that when the attended stimulus was presented in isolation (winner-take-all; WTA). However, attentional modulation is both qualitatively and quantitatively dependent on a neuron's visuospatial tuning. Our results show that during attentive vision, LPFC neuronal ensemble activity can be robustly read out by downstream areas to generate motor commands, and/or fed back into sensory areas to filter out distracter signals in favor of target signals.",
author = "Lyndon Duong and Leavitt, {Matthew L} and Florian Pieper and Sachs, {Adam J.} and Martinez-Trujillo, {Julio C}",
year = "2019",
month = apr,
day = "20",
doi = "https://doi.org/10.1523/ENEURO.0301-18.2019",
language = "English",
volume = "6",
journal = "ENEURO",
issn = "2373-2822",
publisher = "Society for Neuroscience",
number = "2",

}

RIS

TY - JOUR

T1 - A Normalization Circuit Underlying Coding of Spatial Attention in Primate Lateral Prefrontal Cortex.

AU - Duong, Lyndon

AU - Leavitt, Matthew L

AU - Pieper, Florian

AU - Sachs, Adam J.

AU - Martinez-Trujillo, Julio C

PY - 2019/4/20

Y1 - 2019/4/20

N2 - Lateral prefrontal cortex (LPFC) neurons signal the allocation of voluntary attention; however, the neural computations underlying this function remain unknown. To investigate this, we recorded from neuronal ensembles in the LPFC of two Macaca fascicularis performing a visuospatial attention task. LPFC neural responses to a single stimulus were normalized when additional stimuli/distracters appeared across the visual field and were well-characterized by an averaging computation. Deploying attention toward an individual stimulus surrounded by distracters shifted neural activity from an averaging regime toward a regime similar to that when the attended stimulus was presented in isolation (winner-take-all; WTA). However, attentional modulation is both qualitatively and quantitatively dependent on a neuron's visuospatial tuning. Our results show that during attentive vision, LPFC neuronal ensemble activity can be robustly read out by downstream areas to generate motor commands, and/or fed back into sensory areas to filter out distracter signals in favor of target signals.

AB - Lateral prefrontal cortex (LPFC) neurons signal the allocation of voluntary attention; however, the neural computations underlying this function remain unknown. To investigate this, we recorded from neuronal ensembles in the LPFC of two Macaca fascicularis performing a visuospatial attention task. LPFC neural responses to a single stimulus were normalized when additional stimuli/distracters appeared across the visual field and were well-characterized by an averaging computation. Deploying attention toward an individual stimulus surrounded by distracters shifted neural activity from an averaging regime toward a regime similar to that when the attended stimulus was presented in isolation (winner-take-all; WTA). However, attentional modulation is both qualitatively and quantitatively dependent on a neuron's visuospatial tuning. Our results show that during attentive vision, LPFC neuronal ensemble activity can be robustly read out by downstream areas to generate motor commands, and/or fed back into sensory areas to filter out distracter signals in favor of target signals.

U2 - https://doi.org/10.1523/ENEURO.0301-18.2019

DO - https://doi.org/10.1523/ENEURO.0301-18.2019

M3 - SCORING: Journal article

VL - 6

JO - ENEURO

JF - ENEURO

SN - 2373-2822

IS - 2

ER -