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Detection of endogenous circadian rhythms of clock gene mRNA expression in mouse lung tissue using slice cultures

Detection of endogenous circadian rhythms in clock gene mRNA expression requires that mice be sacrificed at regular time intervals over one or more days. This protocol uses culture tissue slices obtained from a single mouse to collect time-course samples. We describe the procedure from preparation o...

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Detalles Bibliográficos
Autores principales: Matsumura, Ritsuko, Node, Koichi, Akashi, Makoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10193295/
https://www.ncbi.nlm.nih.gov/pubmed/37149856
http://dx.doi.org/10.1016/j.xpro.2023.102280
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author Matsumura, Ritsuko
Node, Koichi
Akashi, Makoto
author_facet Matsumura, Ritsuko
Node, Koichi
Akashi, Makoto
author_sort Matsumura, Ritsuko
collection PubMed
description Detection of endogenous circadian rhythms in clock gene mRNA expression requires that mice be sacrificed at regular time intervals over one or more days. This protocol uses culture tissue slices obtained from a single mouse to collect time-course samples. We describe the procedure from preparation of lung slices to rhythmicity analysis of mRNA expression, including details to create handmade culture inserts. This protocol is useful for many mammalian biological clock researchers because it allows a decrease in animal sacrifice. For complete details on the use and execution of this protocol, please refer to Matsumura et al. (2022).(1)
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spelling pubmed-101932952023-05-19 Detection of endogenous circadian rhythms of clock gene mRNA expression in mouse lung tissue using slice cultures Matsumura, Ritsuko Node, Koichi Akashi, Makoto STAR Protoc Protocol Detection of endogenous circadian rhythms in clock gene mRNA expression requires that mice be sacrificed at regular time intervals over one or more days. This protocol uses culture tissue slices obtained from a single mouse to collect time-course samples. We describe the procedure from preparation of lung slices to rhythmicity analysis of mRNA expression, including details to create handmade culture inserts. This protocol is useful for many mammalian biological clock researchers because it allows a decrease in animal sacrifice. For complete details on the use and execution of this protocol, please refer to Matsumura et al. (2022).(1) Elsevier 2023-05-06 /pmc/articles/PMC10193295/ /pubmed/37149856 http://dx.doi.org/10.1016/j.xpro.2023.102280 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Matsumura, Ritsuko
Node, Koichi
Akashi, Makoto
Detection of endogenous circadian rhythms of clock gene mRNA expression in mouse lung tissue using slice cultures
title Detection of endogenous circadian rhythms of clock gene mRNA expression in mouse lung tissue using slice cultures
title_full Detection of endogenous circadian rhythms of clock gene mRNA expression in mouse lung tissue using slice cultures
title_fullStr Detection of endogenous circadian rhythms of clock gene mRNA expression in mouse lung tissue using slice cultures
title_full_unstemmed Detection of endogenous circadian rhythms of clock gene mRNA expression in mouse lung tissue using slice cultures
title_short Detection of endogenous circadian rhythms of clock gene mRNA expression in mouse lung tissue using slice cultures
title_sort detection of endogenous circadian rhythms of clock gene mrna expression in mouse lung tissue using slice cultures
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10193295/
https://www.ncbi.nlm.nih.gov/pubmed/37149856
http://dx.doi.org/10.1016/j.xpro.2023.102280
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