Cargando…
Cell Type-Specific Arousal-Dependent Modulation of Thalamic Activity in the Lateral Geniculate Nucleus
State-dependent thalamocortical activity is important for sensory coding, oscillations, and cognition. The lateral geniculate nucleus (LGN) relays visual information to the cortex, but the state-dependent spontaneous activity of LGN neurons in awake behaving animals remains controversial. Using a co...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152899/ https://www.ncbi.nlm.nih.gov/pubmed/34296165 http://dx.doi.org/10.1093/texcom/tgab020 |
_version_ | 1783698687798542336 |
---|---|
author | Molnár, Benedek Sere, Péter Bordé, Sándor Koós, Krisztián Zsigri, Nikolett Horváth, Péter Lőrincz, Magor L |
author_facet | Molnár, Benedek Sere, Péter Bordé, Sándor Koós, Krisztián Zsigri, Nikolett Horváth, Péter Lőrincz, Magor L |
author_sort | Molnár, Benedek |
collection | PubMed |
description | State-dependent thalamocortical activity is important for sensory coding, oscillations, and cognition. The lateral geniculate nucleus (LGN) relays visual information to the cortex, but the state-dependent spontaneous activity of LGN neurons in awake behaving animals remains controversial. Using a combination of pupillometry, extracellular, and intracellular recordings from identified LGN neurons in behaving mice, we show that thalamocortical (TC) neurons and interneurons are distinctly correlated to arousal forming two complementary coalitions. Intracellular recordings indicated that the membrane potential of LGN TC neurons was tightly correlated to fluctuations in pupil size. Inactivating the corticothalamic feedback to the LGN suppressed the arousal dependency of LGN neurons. Taken together, our results show that LGN neuronal membrane potential and action potential output are dynamically linked to arousal-dependent brain states in awake mice, and this might have important functional implications. |
format | Online Article Text |
id | pubmed-8152899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-81528992021-07-21 Cell Type-Specific Arousal-Dependent Modulation of Thalamic Activity in the Lateral Geniculate Nucleus Molnár, Benedek Sere, Péter Bordé, Sándor Koós, Krisztián Zsigri, Nikolett Horváth, Péter Lőrincz, Magor L Cereb Cortex Commun Original Article State-dependent thalamocortical activity is important for sensory coding, oscillations, and cognition. The lateral geniculate nucleus (LGN) relays visual information to the cortex, but the state-dependent spontaneous activity of LGN neurons in awake behaving animals remains controversial. Using a combination of pupillometry, extracellular, and intracellular recordings from identified LGN neurons in behaving mice, we show that thalamocortical (TC) neurons and interneurons are distinctly correlated to arousal forming two complementary coalitions. Intracellular recordings indicated that the membrane potential of LGN TC neurons was tightly correlated to fluctuations in pupil size. Inactivating the corticothalamic feedback to the LGN suppressed the arousal dependency of LGN neurons. Taken together, our results show that LGN neuronal membrane potential and action potential output are dynamically linked to arousal-dependent brain states in awake mice, and this might have important functional implications. Oxford University Press 2021-03-16 /pmc/articles/PMC8152899/ /pubmed/34296165 http://dx.doi.org/10.1093/texcom/tgab020 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Molnár, Benedek Sere, Péter Bordé, Sándor Koós, Krisztián Zsigri, Nikolett Horváth, Péter Lőrincz, Magor L Cell Type-Specific Arousal-Dependent Modulation of Thalamic Activity in the Lateral Geniculate Nucleus |
title | Cell Type-Specific Arousal-Dependent Modulation of Thalamic Activity in the Lateral Geniculate Nucleus |
title_full | Cell Type-Specific Arousal-Dependent Modulation of Thalamic Activity in the Lateral Geniculate Nucleus |
title_fullStr | Cell Type-Specific Arousal-Dependent Modulation of Thalamic Activity in the Lateral Geniculate Nucleus |
title_full_unstemmed | Cell Type-Specific Arousal-Dependent Modulation of Thalamic Activity in the Lateral Geniculate Nucleus |
title_short | Cell Type-Specific Arousal-Dependent Modulation of Thalamic Activity in the Lateral Geniculate Nucleus |
title_sort | cell type-specific arousal-dependent modulation of thalamic activity in the lateral geniculate nucleus |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152899/ https://www.ncbi.nlm.nih.gov/pubmed/34296165 http://dx.doi.org/10.1093/texcom/tgab020 |
work_keys_str_mv | AT molnarbenedek celltypespecificarousaldependentmodulationofthalamicactivityinthelateralgeniculatenucleus AT serepeter celltypespecificarousaldependentmodulationofthalamicactivityinthelateralgeniculatenucleus AT bordesandor celltypespecificarousaldependentmodulationofthalamicactivityinthelateralgeniculatenucleus AT kooskrisztian celltypespecificarousaldependentmodulationofthalamicactivityinthelateralgeniculatenucleus AT zsigrinikolett celltypespecificarousaldependentmodulationofthalamicactivityinthelateralgeniculatenucleus AT horvathpeter celltypespecificarousaldependentmodulationofthalamicactivityinthelateralgeniculatenucleus AT lorinczmagorl celltypespecificarousaldependentmodulationofthalamicactivityinthelateralgeniculatenucleus |