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Striatal ensemble activity in an innate naturalistic behavior

Self-grooming is an innate, naturalistic behavior found in a wide variety of organisms. The control of rodent grooming has been shown to be mediated by the dorsolateral striatum through lesion studies and in-vivo extracellular recordings. Yet, it is unclear how populations of neurons in the striatum...

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Autores principales: Minkowicz, Samuel, Mathews, Mychaela Alexandria, Mou, Felicia Hoilam, Yoon, Hyoseo, Freda, Sara Nicole, Cui, Ethan S, Kennedy, Ann, Kozorovitskiy, Yevgenia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980072/
https://www.ncbi.nlm.nih.gov/pubmed/36865109
http://dx.doi.org/10.1101/2023.02.23.529669
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author Minkowicz, Samuel
Mathews, Mychaela Alexandria
Mou, Felicia Hoilam
Yoon, Hyoseo
Freda, Sara Nicole
Cui, Ethan S
Kennedy, Ann
Kozorovitskiy, Yevgenia
author_facet Minkowicz, Samuel
Mathews, Mychaela Alexandria
Mou, Felicia Hoilam
Yoon, Hyoseo
Freda, Sara Nicole
Cui, Ethan S
Kennedy, Ann
Kozorovitskiy, Yevgenia
author_sort Minkowicz, Samuel
collection PubMed
description Self-grooming is an innate, naturalistic behavior found in a wide variety of organisms. The control of rodent grooming has been shown to be mediated by the dorsolateral striatum through lesion studies and in-vivo extracellular recordings. Yet, it is unclear how populations of neurons in the striatum encode grooming. We recorded single-unit extracellular activity from populations of neurons in freely moving mice and developed a semi-automated approach to detect self-grooming events from 117 hours of simultaneous multi-camera video recordings of mouse behavior. We first characterized the grooming transition-aligned response profiles of striatal projection neuron and fast spiking interneuron single units. We identified striatal ensembles whose units were more strongly correlated during grooming than during the entire session. These ensembles display varied grooming responses, including transient changes around grooming transitions or sustained changes in activity throughout the duration of grooming. Neural trajectories computed from the identified ensembles retain the grooming related dynamics present in trajectories computed from all units in the session. These results elaborate striatal function in rodent self-grooming and demonstrate that striatal grooming-related activity is organized within functional ensembles, improving our understanding of how the striatum guides action selection in a naturalistic behavior.
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spelling pubmed-99800722023-03-03 Striatal ensemble activity in an innate naturalistic behavior Minkowicz, Samuel Mathews, Mychaela Alexandria Mou, Felicia Hoilam Yoon, Hyoseo Freda, Sara Nicole Cui, Ethan S Kennedy, Ann Kozorovitskiy, Yevgenia bioRxiv Article Self-grooming is an innate, naturalistic behavior found in a wide variety of organisms. The control of rodent grooming has been shown to be mediated by the dorsolateral striatum through lesion studies and in-vivo extracellular recordings. Yet, it is unclear how populations of neurons in the striatum encode grooming. We recorded single-unit extracellular activity from populations of neurons in freely moving mice and developed a semi-automated approach to detect self-grooming events from 117 hours of simultaneous multi-camera video recordings of mouse behavior. We first characterized the grooming transition-aligned response profiles of striatal projection neuron and fast spiking interneuron single units. We identified striatal ensembles whose units were more strongly correlated during grooming than during the entire session. These ensembles display varied grooming responses, including transient changes around grooming transitions or sustained changes in activity throughout the duration of grooming. Neural trajectories computed from the identified ensembles retain the grooming related dynamics present in trajectories computed from all units in the session. These results elaborate striatal function in rodent self-grooming and demonstrate that striatal grooming-related activity is organized within functional ensembles, improving our understanding of how the striatum guides action selection in a naturalistic behavior. Cold Spring Harbor Laboratory 2023-02-23 /pmc/articles/PMC9980072/ /pubmed/36865109 http://dx.doi.org/10.1101/2023.02.23.529669 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Minkowicz, Samuel
Mathews, Mychaela Alexandria
Mou, Felicia Hoilam
Yoon, Hyoseo
Freda, Sara Nicole
Cui, Ethan S
Kennedy, Ann
Kozorovitskiy, Yevgenia
Striatal ensemble activity in an innate naturalistic behavior
title Striatal ensemble activity in an innate naturalistic behavior
title_full Striatal ensemble activity in an innate naturalistic behavior
title_fullStr Striatal ensemble activity in an innate naturalistic behavior
title_full_unstemmed Striatal ensemble activity in an innate naturalistic behavior
title_short Striatal ensemble activity in an innate naturalistic behavior
title_sort striatal ensemble activity in an innate naturalistic behavior
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980072/
https://www.ncbi.nlm.nih.gov/pubmed/36865109
http://dx.doi.org/10.1101/2023.02.23.529669
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