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Seasonal plasticity in GABA(A) signaling is necessary for restoring phase synchrony in the master circadian clock network
Annual changes in the environment threaten survival, and numerous biological processes in mammals adjust to this challenge via seasonal encoding by the suprachiasmatic nucleus (SCN). To tune behavior according to day length, SCN neurons display unified rhythms with synchronous phasing when days are...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6867713/ https://www.ncbi.nlm.nih.gov/pubmed/31746738 http://dx.doi.org/10.7554/eLife.49578 |
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author | Rohr, Kayla E Pancholi, Harshida Haider, Shabi Karow, Christopher Modert, David Raddatz, Nicholas J Evans, Jennifer |
author_facet | Rohr, Kayla E Pancholi, Harshida Haider, Shabi Karow, Christopher Modert, David Raddatz, Nicholas J Evans, Jennifer |
author_sort | Rohr, Kayla E |
collection | PubMed |
description | Annual changes in the environment threaten survival, and numerous biological processes in mammals adjust to this challenge via seasonal encoding by the suprachiasmatic nucleus (SCN). To tune behavior according to day length, SCN neurons display unified rhythms with synchronous phasing when days are short, but will divide into two sub-clusters when days are long. The transition between SCN states is critical for maintaining behavioral responses to seasonal change, but the mechanisms regulating this form of neuroplasticity remain unclear. Here we identify that a switch in chloride transport and GABA(A) signaling is critical for maintaining state plasticity in the SCN network. Further, we reveal that blocking excitatory GABA(A) signaling locks the SCN into its long day state. Collectively, these data demonstrate that plasticity in GABA(A) signaling dictates how clock neurons interact to maintain environmental encoding. Further, this work highlights factors that may influence susceptibility to seasonal disorders in humans. |
format | Online Article Text |
id | pubmed-6867713 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-68677132019-11-23 Seasonal plasticity in GABA(A) signaling is necessary for restoring phase synchrony in the master circadian clock network Rohr, Kayla E Pancholi, Harshida Haider, Shabi Karow, Christopher Modert, David Raddatz, Nicholas J Evans, Jennifer eLife Neuroscience Annual changes in the environment threaten survival, and numerous biological processes in mammals adjust to this challenge via seasonal encoding by the suprachiasmatic nucleus (SCN). To tune behavior according to day length, SCN neurons display unified rhythms with synchronous phasing when days are short, but will divide into two sub-clusters when days are long. The transition between SCN states is critical for maintaining behavioral responses to seasonal change, but the mechanisms regulating this form of neuroplasticity remain unclear. Here we identify that a switch in chloride transport and GABA(A) signaling is critical for maintaining state plasticity in the SCN network. Further, we reveal that blocking excitatory GABA(A) signaling locks the SCN into its long day state. Collectively, these data demonstrate that plasticity in GABA(A) signaling dictates how clock neurons interact to maintain environmental encoding. Further, this work highlights factors that may influence susceptibility to seasonal disorders in humans. eLife Sciences Publications, Ltd 2019-11-20 /pmc/articles/PMC6867713/ /pubmed/31746738 http://dx.doi.org/10.7554/eLife.49578 Text en © 2019, Rohr et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Rohr, Kayla E Pancholi, Harshida Haider, Shabi Karow, Christopher Modert, David Raddatz, Nicholas J Evans, Jennifer Seasonal plasticity in GABA(A) signaling is necessary for restoring phase synchrony in the master circadian clock network |
title | Seasonal plasticity in GABA(A) signaling is necessary for restoring phase synchrony in the master circadian clock network |
title_full | Seasonal plasticity in GABA(A) signaling is necessary for restoring phase synchrony in the master circadian clock network |
title_fullStr | Seasonal plasticity in GABA(A) signaling is necessary for restoring phase synchrony in the master circadian clock network |
title_full_unstemmed | Seasonal plasticity in GABA(A) signaling is necessary for restoring phase synchrony in the master circadian clock network |
title_short | Seasonal plasticity in GABA(A) signaling is necessary for restoring phase synchrony in the master circadian clock network |
title_sort | seasonal plasticity in gaba(a) signaling is necessary for restoring phase synchrony in the master circadian clock network |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6867713/ https://www.ncbi.nlm.nih.gov/pubmed/31746738 http://dx.doi.org/10.7554/eLife.49578 |
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