Stability of d-luciferin for bioluminescence to detect gene expression in freely moving mice for long durations.


Journal

Luminescence : the journal of biological and chemical luminescence
ISSN: 1522-7243
Titre abrégé: Luminescence
Pays: England
ID NLM: 100889025

Informations de publication

Date de publication:
Feb 2021
Historique:
received: 12 06 2020
revised: 14 07 2020
accepted: 20 07 2020
pubmed: 29 7 2020
medline: 29 7 2021
entrez: 29 7 2020
Statut: ppublish

Résumé

Circadian disturbance of clock gene expression is a risk factor for diseases such as obesity, cancer, and sleep disorders. To study these diseases, it is necessary to monitor and analyze the expression rhythm of clock genes in the whole body for a long duration. The bioluminescent reporter enzyme firefly luciferase and its substrate d-luciferin have been used to generate optical signals from tissues in vivo with high sensitivity. However, little information is known about the stability of d-luciferin to detect gene expression in living animals for a long duration. In the present study, we examined the stability of a luciferin solution over 21 days. l-Luciferin, which is synthesized using racemization of d-luciferin, was at high concentrations after 21 days. In addition, we showed that bioluminescence of Period1 (Per1) expression in the liver was significantly decreased compared with the day 1 solution, although locomotor activity rhythm was not affected. These results showed that d-luciferin should be applied to the mouse within, at most, 7 days to detect bioluminescence of Per1 gene expression rhythm in vivo.

Identifiants

pubmed: 32721066
doi: 10.1002/bio.3917
doi:

Substances chimiques

Benzothiazoles 0
D-luciferin 0
Firefly Luciferin 5TBB02N29K
Luciferases, Firefly EC 1.13.12.7

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

94-98

Subventions

Organisme : JSPS KAKENHI
ID : 17H04022
Organisme : JSPS KAKENHI
ID : 18H04724
Organisme : 'Resonance Bio'

Informations de copyright

© 2020 John Wiley & Sons, Ltd.

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Auteurs

Kanako Nakajima (K)

Department of Pharmaceutical Sciences, International University of Health and Welfare, Ohtawara, Tochigi, Japan.

Kazuko Hamada (K)

Department of Pharmaceutical Sciences, International University of Health and Welfare, Ohtawara, Tochigi, Japan.

Ryoga Ito (R)

Department of Pharmaceutical Sciences, International University of Health and Welfare, Ohtawara, Tochigi, Japan.

Yukina Yoshida (Y)

Department of Pharmaceutical Sciences, International University of Health and Welfare, Ohtawara, Tochigi, Japan.

Kenneth Sutherland (K)

Global Center for Biomedical Science and Engineering, Faculty of Medicine, Hokkaido University, Sapporo, Hokkaido, Japan.

Masayori Ishikawa (M)

Global Center for Biomedical Science and Engineering, Faculty of Medicine, Hokkaido University, Sapporo, Hokkaido, Japan.
Faculty of Health Sciences, Hokkaido University, Sapporo, Hokkaido, Japan.

Michitaka Ozaki (M)

Department of Biological Response and Regulation, Faculty of Health Sciences, Hokkaido University, Sapporo, Hokkaido, Japan.

Hiroki Shirato (H)

Global Center for Biomedical Science and Engineering, Faculty of Medicine, Hokkaido University, Sapporo, Hokkaido, Japan.
Department of Proton Beam Therapy, Research Center for Collaborative Projects, Faculty of Medicine, Hokkaido University, Sapporo, Hokkaido, Japan.

Toshiyuki Hamada (T)

Department of Pharmaceutical Sciences, International University of Health and Welfare, Ohtawara, Tochigi, Japan.
Department of Biological Response and Regulation, Faculty of Health Sciences, Hokkaido University, Sapporo, Hokkaido, Japan.
Hakujikai Institute of Gerontology, 5-11-1, Shikahama, Adachi Ward, Tokyo, Japan.

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