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Non-invasive in vivo imaging of UCP1 expression in live mice via near-infrared fluorescent protein iRFP720

Uncoupling protein 1 (UCP1) is a mitochondrial protein that is expressed in both brown and beige adipocytes. UCP1 uncouples the mitochondrial electron transport chain from ATP synthesis to produce heat via non-shivering thermogenesis. Due to their ability to dissipate energy as heat and ameliorate m...

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Autores principales: Fukuda, Aya, Honda, Shiho, Fujioka, Norie, Sekiguchi, Yuya, Mizuno, Seiya, Miwa, Yoshihiro, Sugiyama, Fumihiro, Hayashi, Yohei, Nishimura, Ken, Hisatake, Koji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857924/
https://www.ncbi.nlm.nih.gov/pubmed/31730675
http://dx.doi.org/10.1371/journal.pone.0225213
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author Fukuda, Aya
Honda, Shiho
Fujioka, Norie
Sekiguchi, Yuya
Mizuno, Seiya
Miwa, Yoshihiro
Sugiyama, Fumihiro
Hayashi, Yohei
Nishimura, Ken
Hisatake, Koji
author_facet Fukuda, Aya
Honda, Shiho
Fujioka, Norie
Sekiguchi, Yuya
Mizuno, Seiya
Miwa, Yoshihiro
Sugiyama, Fumihiro
Hayashi, Yohei
Nishimura, Ken
Hisatake, Koji
author_sort Fukuda, Aya
collection PubMed
description Uncoupling protein 1 (UCP1) is a mitochondrial protein that is expressed in both brown and beige adipocytes. UCP1 uncouples the mitochondrial electron transport chain from ATP synthesis to produce heat via non-shivering thermogenesis. Due to their ability to dissipate energy as heat and ameliorate metabolic disorders, UCP1-expressing adipocytes are considered as a potential target for anti-obesity treatment. To monitor the expression of UCP1 in live mice in a non-invasive manner, we generated the Ucp1-iRFP720 knock-in (Ucp1-iRFP720 KI) mice, in which the gene encoding a near-infrared fluorescent protein iRFP720 is inserted into the Ucp1 gene locus. Using the heterozygous Ucp1-iRFP720 KI mice, we observed robust iRFP fluorescence in the interscapular region where brown adipose tissue is located. Moreover, the iRFP fluorescence was clearly observable in inguinal white adipose tissues in live mice administered with β3-adrenergic receptor agonist CL316,243. We also found that the homozygous Ucp1-iRFP720 KI mice, which are deficient in UCP1, displayed prominent iRFP fluorescence in the inguinal regions at the standard housing temperature. Consistent with this, the mice exhibited expanded populations of beige-like adipocytes in inguinal white adipose tissue, in which the Ucp1 promoter was dramatically activated. Thus, the Ucp1-iRFP720 KI mice provide a convenient model for non-invasive in vivo imaging of UCP1 expression in both brown and beige adipocytes in live mice.
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spelling pubmed-68579242019-12-07 Non-invasive in vivo imaging of UCP1 expression in live mice via near-infrared fluorescent protein iRFP720 Fukuda, Aya Honda, Shiho Fujioka, Norie Sekiguchi, Yuya Mizuno, Seiya Miwa, Yoshihiro Sugiyama, Fumihiro Hayashi, Yohei Nishimura, Ken Hisatake, Koji PLoS One Research Article Uncoupling protein 1 (UCP1) is a mitochondrial protein that is expressed in both brown and beige adipocytes. UCP1 uncouples the mitochondrial electron transport chain from ATP synthesis to produce heat via non-shivering thermogenesis. Due to their ability to dissipate energy as heat and ameliorate metabolic disorders, UCP1-expressing adipocytes are considered as a potential target for anti-obesity treatment. To monitor the expression of UCP1 in live mice in a non-invasive manner, we generated the Ucp1-iRFP720 knock-in (Ucp1-iRFP720 KI) mice, in which the gene encoding a near-infrared fluorescent protein iRFP720 is inserted into the Ucp1 gene locus. Using the heterozygous Ucp1-iRFP720 KI mice, we observed robust iRFP fluorescence in the interscapular region where brown adipose tissue is located. Moreover, the iRFP fluorescence was clearly observable in inguinal white adipose tissues in live mice administered with β3-adrenergic receptor agonist CL316,243. We also found that the homozygous Ucp1-iRFP720 KI mice, which are deficient in UCP1, displayed prominent iRFP fluorescence in the inguinal regions at the standard housing temperature. Consistent with this, the mice exhibited expanded populations of beige-like adipocytes in inguinal white adipose tissue, in which the Ucp1 promoter was dramatically activated. Thus, the Ucp1-iRFP720 KI mice provide a convenient model for non-invasive in vivo imaging of UCP1 expression in both brown and beige adipocytes in live mice. Public Library of Science 2019-11-15 /pmc/articles/PMC6857924/ /pubmed/31730675 http://dx.doi.org/10.1371/journal.pone.0225213 Text en © 2019 Fukuda et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Fukuda, Aya
Honda, Shiho
Fujioka, Norie
Sekiguchi, Yuya
Mizuno, Seiya
Miwa, Yoshihiro
Sugiyama, Fumihiro
Hayashi, Yohei
Nishimura, Ken
Hisatake, Koji
Non-invasive in vivo imaging of UCP1 expression in live mice via near-infrared fluorescent protein iRFP720
title Non-invasive in vivo imaging of UCP1 expression in live mice via near-infrared fluorescent protein iRFP720
title_full Non-invasive in vivo imaging of UCP1 expression in live mice via near-infrared fluorescent protein iRFP720
title_fullStr Non-invasive in vivo imaging of UCP1 expression in live mice via near-infrared fluorescent protein iRFP720
title_full_unstemmed Non-invasive in vivo imaging of UCP1 expression in live mice via near-infrared fluorescent protein iRFP720
title_short Non-invasive in vivo imaging of UCP1 expression in live mice via near-infrared fluorescent protein iRFP720
title_sort non-invasive in vivo imaging of ucp1 expression in live mice via near-infrared fluorescent protein irfp720
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857924/
https://www.ncbi.nlm.nih.gov/pubmed/31730675
http://dx.doi.org/10.1371/journal.pone.0225213
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