Cargando…
Selective modulation of cortical population dynamics during neuroprosthetic skill learning
Brain-machine interfaces (BMIs) provide a framework for studying how cortical population dynamics evolve over learning in a task in which the mapping between neural activity and behavior is precisely defined. Learning to control a BMI is associated with the emergence of coordinated neural dynamics i...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9509316/ https://www.ncbi.nlm.nih.gov/pubmed/36153356 http://dx.doi.org/10.1038/s41598-022-20218-3 |
_version_ | 1784797212137488384 |
---|---|
author | Zippi, Ellen L. You, Albert K. Ganguly, Karunesh Carmena, Jose M. |
author_facet | Zippi, Ellen L. You, Albert K. Ganguly, Karunesh Carmena, Jose M. |
author_sort | Zippi, Ellen L. |
collection | PubMed |
description | Brain-machine interfaces (BMIs) provide a framework for studying how cortical population dynamics evolve over learning in a task in which the mapping between neural activity and behavior is precisely defined. Learning to control a BMI is associated with the emergence of coordinated neural dynamics in populations of neurons whose activity serves as direct input to the BMI decoder (direct subpopulation). While previous work shows differential modification of firing rate modulation in this population relative to a population whose activity was not directly input to the BMI decoder (indirect subpopulation), little is known about how learning-related changes in cortical population dynamics within these groups compare.To investigate this, we monitored both direct and indirect subpopulations as two macaque monkeys learned to control a BMI. We found that while the combined population increased coordinated neural dynamics, this increase in coordination was primarily driven by changes in the direct subpopulation. These findings suggest that motor cortex refines cortical dynamics by increasing neural variance throughout the entire population during learning, with a more pronounced coordination of firing activity in subpopulations that are causally linked to behavior. |
format | Online Article Text |
id | pubmed-9509316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95093162022-09-26 Selective modulation of cortical population dynamics during neuroprosthetic skill learning Zippi, Ellen L. You, Albert K. Ganguly, Karunesh Carmena, Jose M. Sci Rep Article Brain-machine interfaces (BMIs) provide a framework for studying how cortical population dynamics evolve over learning in a task in which the mapping between neural activity and behavior is precisely defined. Learning to control a BMI is associated with the emergence of coordinated neural dynamics in populations of neurons whose activity serves as direct input to the BMI decoder (direct subpopulation). While previous work shows differential modification of firing rate modulation in this population relative to a population whose activity was not directly input to the BMI decoder (indirect subpopulation), little is known about how learning-related changes in cortical population dynamics within these groups compare.To investigate this, we monitored both direct and indirect subpopulations as two macaque monkeys learned to control a BMI. We found that while the combined population increased coordinated neural dynamics, this increase in coordination was primarily driven by changes in the direct subpopulation. These findings suggest that motor cortex refines cortical dynamics by increasing neural variance throughout the entire population during learning, with a more pronounced coordination of firing activity in subpopulations that are causally linked to behavior. Nature Publishing Group UK 2022-09-24 /pmc/articles/PMC9509316/ /pubmed/36153356 http://dx.doi.org/10.1038/s41598-022-20218-3 Text en © The Author(s) 2022 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zippi, Ellen L. You, Albert K. Ganguly, Karunesh Carmena, Jose M. Selective modulation of cortical population dynamics during neuroprosthetic skill learning |
title | Selective modulation of cortical population dynamics during neuroprosthetic skill learning |
title_full | Selective modulation of cortical population dynamics during neuroprosthetic skill learning |
title_fullStr | Selective modulation of cortical population dynamics during neuroprosthetic skill learning |
title_full_unstemmed | Selective modulation of cortical population dynamics during neuroprosthetic skill learning |
title_short | Selective modulation of cortical population dynamics during neuroprosthetic skill learning |
title_sort | selective modulation of cortical population dynamics during neuroprosthetic skill learning |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9509316/ https://www.ncbi.nlm.nih.gov/pubmed/36153356 http://dx.doi.org/10.1038/s41598-022-20218-3 |
work_keys_str_mv | AT zippiellenl selectivemodulationofcorticalpopulationdynamicsduringneuroprostheticskilllearning AT youalbertk selectivemodulationofcorticalpopulationdynamicsduringneuroprostheticskilllearning AT gangulykarunesh selectivemodulationofcorticalpopulationdynamicsduringneuroprostheticskilllearning AT carmenajosem selectivemodulationofcorticalpopulationdynamicsduringneuroprostheticskilllearning |