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Retina-attached slice recording reveals light-triggered tonic GABA signaling in suprachiasmatic nucleus

Light is a powerful external cue modulating the biological rhythm of internal clock neurons in the suprachiasmatic nucleus (SCN). GABA signaling in SCN is critically involved in this process. Both phasic and tonic modes of GABA signaling exist in SCN. Of the two modes, the tonic mode of GABA signali...

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Autores principales: Kwon, Jea, Jang, Minwoo Wendy, Lee, C. Justin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626980/
https://www.ncbi.nlm.nih.gov/pubmed/34838118
http://dx.doi.org/10.1186/s13041-021-00881-9
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author Kwon, Jea
Jang, Minwoo Wendy
Lee, C. Justin
author_facet Kwon, Jea
Jang, Minwoo Wendy
Lee, C. Justin
author_sort Kwon, Jea
collection PubMed
description Light is a powerful external cue modulating the biological rhythm of internal clock neurons in the suprachiasmatic nucleus (SCN). GABA signaling in SCN is critically involved in this process. Both phasic and tonic modes of GABA signaling exist in SCN. Of the two modes, the tonic mode of GABA signaling has been implicated in light-mediated synchrony of SCN neurons. However, modulatory effects of external light on tonic GABA signalling are yet to be explored. Here, we systematically characterized electrophysiological properties of the clock neurons and determined the spatio-temporal profiles of tonic GABA current. Based on the whole-cell patch-clamp recordings from 76 SCN neurons, the cells with large tonic GABA current (>15 pA) were more frequently found in dorsal SCN. Moreover, tonic GABA current in SCN was highly correlated with the frequency of spontaneous inhibitory postsynaptic current (sIPSC), raising a possibility that tonic GABA current is due to spill-over from synaptic release. Interestingly, tonic GABA current was inversely correlated with slice-to-patch time interval, suggesting a critical role of retinal light exposure in intact brain for an induction of tonic GABA current in SCN. To test this possibility, we obtained meticulously prepared retina-attached SCN slices and successfully recorded tonic and phasic GABA signaling in SCN neurons. For the first time, we observed an early-onset, long-lasting tonic GABA current, followed by a slow-onset, short-lasting increase in the phasic GABA frequency, upon direct light-illumination of the attached retina. This result provides the first evidence that external light cue can directly trigger both tonic and phasic GABA signaling in SCN cell. In conclusion, we propose tonic GABA as the key mediator of external light in SCN. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13041-021-00881-9.
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spelling pubmed-86269802021-11-30 Retina-attached slice recording reveals light-triggered tonic GABA signaling in suprachiasmatic nucleus Kwon, Jea Jang, Minwoo Wendy Lee, C. Justin Mol Brain Short Report Light is a powerful external cue modulating the biological rhythm of internal clock neurons in the suprachiasmatic nucleus (SCN). GABA signaling in SCN is critically involved in this process. Both phasic and tonic modes of GABA signaling exist in SCN. Of the two modes, the tonic mode of GABA signaling has been implicated in light-mediated synchrony of SCN neurons. However, modulatory effects of external light on tonic GABA signalling are yet to be explored. Here, we systematically characterized electrophysiological properties of the clock neurons and determined the spatio-temporal profiles of tonic GABA current. Based on the whole-cell patch-clamp recordings from 76 SCN neurons, the cells with large tonic GABA current (>15 pA) were more frequently found in dorsal SCN. Moreover, tonic GABA current in SCN was highly correlated with the frequency of spontaneous inhibitory postsynaptic current (sIPSC), raising a possibility that tonic GABA current is due to spill-over from synaptic release. Interestingly, tonic GABA current was inversely correlated with slice-to-patch time interval, suggesting a critical role of retinal light exposure in intact brain for an induction of tonic GABA current in SCN. To test this possibility, we obtained meticulously prepared retina-attached SCN slices and successfully recorded tonic and phasic GABA signaling in SCN neurons. For the first time, we observed an early-onset, long-lasting tonic GABA current, followed by a slow-onset, short-lasting increase in the phasic GABA frequency, upon direct light-illumination of the attached retina. This result provides the first evidence that external light cue can directly trigger both tonic and phasic GABA signaling in SCN cell. In conclusion, we propose tonic GABA as the key mediator of external light in SCN. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13041-021-00881-9. BioMed Central 2021-11-27 /pmc/articles/PMC8626980/ /pubmed/34838118 http://dx.doi.org/10.1186/s13041-021-00881-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Short Report
Kwon, Jea
Jang, Minwoo Wendy
Lee, C. Justin
Retina-attached slice recording reveals light-triggered tonic GABA signaling in suprachiasmatic nucleus
title Retina-attached slice recording reveals light-triggered tonic GABA signaling in suprachiasmatic nucleus
title_full Retina-attached slice recording reveals light-triggered tonic GABA signaling in suprachiasmatic nucleus
title_fullStr Retina-attached slice recording reveals light-triggered tonic GABA signaling in suprachiasmatic nucleus
title_full_unstemmed Retina-attached slice recording reveals light-triggered tonic GABA signaling in suprachiasmatic nucleus
title_short Retina-attached slice recording reveals light-triggered tonic GABA signaling in suprachiasmatic nucleus
title_sort retina-attached slice recording reveals light-triggered tonic gaba signaling in suprachiasmatic nucleus
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626980/
https://www.ncbi.nlm.nih.gov/pubmed/34838118
http://dx.doi.org/10.1186/s13041-021-00881-9
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