Cargando…

Targeted V1 comodulation supports task-adaptive sensory decisions

Sensory-guided behavior requires reliable encoding of stimulus information in neural populations, and flexible, task-specific readout. The former has been studied extensively, but the latter remains poorly understood. We introduce a theory for adaptive sensory processing based on functionally-target...

Descripción completa

Detalles Bibliográficos
Autores principales: Haimerl, Caroline, Ruff, Douglas A., Cohen, Marlene R., Savin, Cristina, Simoncelli, Eero P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10689451/
https://www.ncbi.nlm.nih.gov/pubmed/38036519
http://dx.doi.org/10.1038/s41467-023-43432-7
_version_ 1785152370554961920
author Haimerl, Caroline
Ruff, Douglas A.
Cohen, Marlene R.
Savin, Cristina
Simoncelli, Eero P.
author_facet Haimerl, Caroline
Ruff, Douglas A.
Cohen, Marlene R.
Savin, Cristina
Simoncelli, Eero P.
author_sort Haimerl, Caroline
collection PubMed
description Sensory-guided behavior requires reliable encoding of stimulus information in neural populations, and flexible, task-specific readout. The former has been studied extensively, but the latter remains poorly understood. We introduce a theory for adaptive sensory processing based on functionally-targeted stochastic modulation. We show that responses of neurons in area V1 of monkeys performing a visual discrimination task exhibit low-dimensional, rapidly fluctuating gain modulation, which is stronger in task-informative neurons and can be used to decode from neural activity after few training trials, consistent with observed behavior. In a simulated hierarchical neural network model, such labels are learned quickly and can be used to adapt downstream readout, even after several intervening processing stages. Consistently, we find the modulatory signal estimated in V1 is also present in the activity of simultaneously recorded MT units, and is again strongest in task-informative neurons. These results support the idea that co-modulation facilitates task-adaptive hierarchical information routing.
format Online
Article
Text
id pubmed-10689451
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-106894512023-12-02 Targeted V1 comodulation supports task-adaptive sensory decisions Haimerl, Caroline Ruff, Douglas A. Cohen, Marlene R. Savin, Cristina Simoncelli, Eero P. Nat Commun Article Sensory-guided behavior requires reliable encoding of stimulus information in neural populations, and flexible, task-specific readout. The former has been studied extensively, but the latter remains poorly understood. We introduce a theory for adaptive sensory processing based on functionally-targeted stochastic modulation. We show that responses of neurons in area V1 of monkeys performing a visual discrimination task exhibit low-dimensional, rapidly fluctuating gain modulation, which is stronger in task-informative neurons and can be used to decode from neural activity after few training trials, consistent with observed behavior. In a simulated hierarchical neural network model, such labels are learned quickly and can be used to adapt downstream readout, even after several intervening processing stages. Consistently, we find the modulatory signal estimated in V1 is also present in the activity of simultaneously recorded MT units, and is again strongest in task-informative neurons. These results support the idea that co-modulation facilitates task-adaptive hierarchical information routing. Nature Publishing Group UK 2023-11-30 /pmc/articles/PMC10689451/ /pubmed/38036519 http://dx.doi.org/10.1038/s41467-023-43432-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Haimerl, Caroline
Ruff, Douglas A.
Cohen, Marlene R.
Savin, Cristina
Simoncelli, Eero P.
Targeted V1 comodulation supports task-adaptive sensory decisions
title Targeted V1 comodulation supports task-adaptive sensory decisions
title_full Targeted V1 comodulation supports task-adaptive sensory decisions
title_fullStr Targeted V1 comodulation supports task-adaptive sensory decisions
title_full_unstemmed Targeted V1 comodulation supports task-adaptive sensory decisions
title_short Targeted V1 comodulation supports task-adaptive sensory decisions
title_sort targeted v1 comodulation supports task-adaptive sensory decisions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10689451/
https://www.ncbi.nlm.nih.gov/pubmed/38036519
http://dx.doi.org/10.1038/s41467-023-43432-7
work_keys_str_mv AT haimerlcaroline targetedv1comodulationsupportstaskadaptivesensorydecisions
AT ruffdouglasa targetedv1comodulationsupportstaskadaptivesensorydecisions
AT cohenmarlener targetedv1comodulationsupportstaskadaptivesensorydecisions
AT savincristina targetedv1comodulationsupportstaskadaptivesensorydecisions
AT simoncellieerop targetedv1comodulationsupportstaskadaptivesensorydecisions