Cargando…

Gain Modulation by Corticostriatal and Thalamostriatal Input Signals during Reward-Conditioned Behavior

The cortex and thalamus send excitatory projections to the striatum, but little is known about how these inputs, either individually or collectively, regulate striatal dynamics during behavior. The lateral striatum receives overlapping input from the secondary motor cortex (M2), an area involved in...

Descripción completa

Detalles Bibliográficos
Autores principales: Lee, Kwang, Bakhurin, Konstantin I., Claar, Leslie D., Holley, Sandra M., Chong, Natalie C., Cepeda, Carlos, Levine, Michael S., Masmanidis, Sotiris C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6907740/
https://www.ncbi.nlm.nih.gov/pubmed/31747611
http://dx.doi.org/10.1016/j.celrep.2019.10.060
_version_ 1783478586242498560
author Lee, Kwang
Bakhurin, Konstantin I.
Claar, Leslie D.
Holley, Sandra M.
Chong, Natalie C.
Cepeda, Carlos
Levine, Michael S.
Masmanidis, Sotiris C.
author_facet Lee, Kwang
Bakhurin, Konstantin I.
Claar, Leslie D.
Holley, Sandra M.
Chong, Natalie C.
Cepeda, Carlos
Levine, Michael S.
Masmanidis, Sotiris C.
author_sort Lee, Kwang
collection PubMed
description The cortex and thalamus send excitatory projections to the striatum, but little is known about how these inputs, either individually or collectively, regulate striatal dynamics during behavior. The lateral striatum receives overlapping input from the secondary motor cortex (M2), an area involved in licking, and the parafascicular thalamic nucleus (PF). Using neural recordings, together with optogenetic terminal inhibition, we examine the contribution of M2 and PF projections on medium spiny projection neuron (MSN) activity as mice performed an anticipatory licking task. Each input has a similar contribution to striatal activity. By comparing how suppressing single or multiple projections altered striatal activity, we find that cortical and thalamic input signals modulate MSN gain and that this effect is more pronounced in a temporally specific period of the task following the cue presentation. These results demonstrate that cortical and thalamic inputs synergistically regulate striatal output during reward-conditioned behavior.
format Online
Article
Text
id pubmed-6907740
institution National Center for Biotechnology Information
language English
publishDate 2019
record_format MEDLINE/PubMed
spelling pubmed-69077402019-12-12 Gain Modulation by Corticostriatal and Thalamostriatal Input Signals during Reward-Conditioned Behavior Lee, Kwang Bakhurin, Konstantin I. Claar, Leslie D. Holley, Sandra M. Chong, Natalie C. Cepeda, Carlos Levine, Michael S. Masmanidis, Sotiris C. Cell Rep Article The cortex and thalamus send excitatory projections to the striatum, but little is known about how these inputs, either individually or collectively, regulate striatal dynamics during behavior. The lateral striatum receives overlapping input from the secondary motor cortex (M2), an area involved in licking, and the parafascicular thalamic nucleus (PF). Using neural recordings, together with optogenetic terminal inhibition, we examine the contribution of M2 and PF projections on medium spiny projection neuron (MSN) activity as mice performed an anticipatory licking task. Each input has a similar contribution to striatal activity. By comparing how suppressing single or multiple projections altered striatal activity, we find that cortical and thalamic input signals modulate MSN gain and that this effect is more pronounced in a temporally specific period of the task following the cue presentation. These results demonstrate that cortical and thalamic inputs synergistically regulate striatal output during reward-conditioned behavior. 2019-11-19 /pmc/articles/PMC6907740/ /pubmed/31747611 http://dx.doi.org/10.1016/j.celrep.2019.10.060 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Lee, Kwang
Bakhurin, Konstantin I.
Claar, Leslie D.
Holley, Sandra M.
Chong, Natalie C.
Cepeda, Carlos
Levine, Michael S.
Masmanidis, Sotiris C.
Gain Modulation by Corticostriatal and Thalamostriatal Input Signals during Reward-Conditioned Behavior
title Gain Modulation by Corticostriatal and Thalamostriatal Input Signals during Reward-Conditioned Behavior
title_full Gain Modulation by Corticostriatal and Thalamostriatal Input Signals during Reward-Conditioned Behavior
title_fullStr Gain Modulation by Corticostriatal and Thalamostriatal Input Signals during Reward-Conditioned Behavior
title_full_unstemmed Gain Modulation by Corticostriatal and Thalamostriatal Input Signals during Reward-Conditioned Behavior
title_short Gain Modulation by Corticostriatal and Thalamostriatal Input Signals during Reward-Conditioned Behavior
title_sort gain modulation by corticostriatal and thalamostriatal input signals during reward-conditioned behavior
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6907740/
https://www.ncbi.nlm.nih.gov/pubmed/31747611
http://dx.doi.org/10.1016/j.celrep.2019.10.060
work_keys_str_mv AT leekwang gainmodulationbycorticostriatalandthalamostriatalinputsignalsduringrewardconditionedbehavior
AT bakhurinkonstantini gainmodulationbycorticostriatalandthalamostriatalinputsignalsduringrewardconditionedbehavior
AT claarleslied gainmodulationbycorticostriatalandthalamostriatalinputsignalsduringrewardconditionedbehavior
AT holleysandram gainmodulationbycorticostriatalandthalamostriatalinputsignalsduringrewardconditionedbehavior
AT chongnataliec gainmodulationbycorticostriatalandthalamostriatalinputsignalsduringrewardconditionedbehavior
AT cepedacarlos gainmodulationbycorticostriatalandthalamostriatalinputsignalsduringrewardconditionedbehavior
AT levinemichaels gainmodulationbycorticostriatalandthalamostriatalinputsignalsduringrewardconditionedbehavior
AT masmanidissotirisc gainmodulationbycorticostriatalandthalamostriatalinputsignalsduringrewardconditionedbehavior