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In vivo recording of the circadian calcium rhythm in Prokineticin 2 neurons of the suprachiasmatic nucleus

Prokineticin 2 (Prok2) is a small protein expressed in a subpopulation of neurons in the suprachiasmatic nucleus (SCN), the primary circadian pacemaker in mammals. Prok2 has been implicated as a candidate output molecule from the SCN to control multiple circadian rhythms. Genetic manipulation specif...

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Autores principales: Onodera, Kaito, Tsuno, Yusuke, Hiraoka, Yuichi, Tanaka, Kohichi, Maejima, Takashi, Mieda, Michihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562406/
https://www.ncbi.nlm.nih.gov/pubmed/37813987
http://dx.doi.org/10.1038/s41598-023-44282-5
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author Onodera, Kaito
Tsuno, Yusuke
Hiraoka, Yuichi
Tanaka, Kohichi
Maejima, Takashi
Mieda, Michihiro
author_facet Onodera, Kaito
Tsuno, Yusuke
Hiraoka, Yuichi
Tanaka, Kohichi
Maejima, Takashi
Mieda, Michihiro
author_sort Onodera, Kaito
collection PubMed
description Prokineticin 2 (Prok2) is a small protein expressed in a subpopulation of neurons in the suprachiasmatic nucleus (SCN), the primary circadian pacemaker in mammals. Prok2 has been implicated as a candidate output molecule from the SCN to control multiple circadian rhythms. Genetic manipulation specific to Prok2-producing neurons would be a powerful approach to understanding their function. Here, we report the generation of Prok2-tTA knock-in mice expressing the tetracycline transactivator (tTA) specifically in Prok2 neurons and an application of these mice to in vivo recording of Ca(2+) rhythms in these neurons. First, the specific and efficient expression of tTA in Prok2 neurons was verified by crossing the mice with EGFP reporter mice. Prok2-tTA mice were then used to express a fluorescent Ca(2+) sensor protein to record the circadian Ca(2+) rhythm in SCN Prok2 neurons in vivo. Ca(2+) in these cells showed clear circadian rhythms in both light–dark and constant dark conditions, with their peaks around midday. Notably, the hours of high Ca(2+) nearly coincided with the rest period of the behavioral rhythm. These observations fit well with the predicted function of Prok2 neurons as a candidate output pathway of the SCN by suppressing locomotor activity during both daytime and subjective daytime.
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spelling pubmed-105624062023-10-11 In vivo recording of the circadian calcium rhythm in Prokineticin 2 neurons of the suprachiasmatic nucleus Onodera, Kaito Tsuno, Yusuke Hiraoka, Yuichi Tanaka, Kohichi Maejima, Takashi Mieda, Michihiro Sci Rep Article Prokineticin 2 (Prok2) is a small protein expressed in a subpopulation of neurons in the suprachiasmatic nucleus (SCN), the primary circadian pacemaker in mammals. Prok2 has been implicated as a candidate output molecule from the SCN to control multiple circadian rhythms. Genetic manipulation specific to Prok2-producing neurons would be a powerful approach to understanding their function. Here, we report the generation of Prok2-tTA knock-in mice expressing the tetracycline transactivator (tTA) specifically in Prok2 neurons and an application of these mice to in vivo recording of Ca(2+) rhythms in these neurons. First, the specific and efficient expression of tTA in Prok2 neurons was verified by crossing the mice with EGFP reporter mice. Prok2-tTA mice were then used to express a fluorescent Ca(2+) sensor protein to record the circadian Ca(2+) rhythm in SCN Prok2 neurons in vivo. Ca(2+) in these cells showed clear circadian rhythms in both light–dark and constant dark conditions, with their peaks around midday. Notably, the hours of high Ca(2+) nearly coincided with the rest period of the behavioral rhythm. These observations fit well with the predicted function of Prok2 neurons as a candidate output pathway of the SCN by suppressing locomotor activity during both daytime and subjective daytime. Nature Publishing Group UK 2023-10-09 /pmc/articles/PMC10562406/ /pubmed/37813987 http://dx.doi.org/10.1038/s41598-023-44282-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Article
Onodera, Kaito
Tsuno, Yusuke
Hiraoka, Yuichi
Tanaka, Kohichi
Maejima, Takashi
Mieda, Michihiro
In vivo recording of the circadian calcium rhythm in Prokineticin 2 neurons of the suprachiasmatic nucleus
title In vivo recording of the circadian calcium rhythm in Prokineticin 2 neurons of the suprachiasmatic nucleus
title_full In vivo recording of the circadian calcium rhythm in Prokineticin 2 neurons of the suprachiasmatic nucleus
title_fullStr In vivo recording of the circadian calcium rhythm in Prokineticin 2 neurons of the suprachiasmatic nucleus
title_full_unstemmed In vivo recording of the circadian calcium rhythm in Prokineticin 2 neurons of the suprachiasmatic nucleus
title_short In vivo recording of the circadian calcium rhythm in Prokineticin 2 neurons of the suprachiasmatic nucleus
title_sort in vivo recording of the circadian calcium rhythm in prokineticin 2 neurons of the suprachiasmatic nucleus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562406/
https://www.ncbi.nlm.nih.gov/pubmed/37813987
http://dx.doi.org/10.1038/s41598-023-44282-5
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