Evidence map›Paper›PMID 31730675›Full record

ArticlePloS one2019

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

Aya Fukuda, Shiho Honda, Norie Fujioka, Yuya Sekiguchi, Seiya Mizuno, Yoshihiro Miwa, Fumihiro Sugiyama, Yohei Hayashi, Ken Nishimura, Koji Hisatake

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Non-invasive Reporter Gene Imaging of Cell Therapies, including T Cells and Stem Cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Review
  9. How Non-invasiveFrontiers in physiology · 2020
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Aya FukudaLaboratory of Gene Regulation, University of Tsukuba, Tsukuba, Ibaraki, Japan.ORCID 0000-0002-4960-7028
Shiho HondaLaboratory of Gene Regulation, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Norie FujiokaLaboratory of Gene Regulation, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Yuya SekiguchiLaboratory of Gene Regulation, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Seiya MizunoLaboratory of Animal Science, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Yoshihiro MiwaLaboratory of Anatomy and Embryology, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Fumihiro SugiyamaLaboratory of Animal Science, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Yohei HayashiLaboratory of Gene Regulation, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Ken NishimuraLaboratory of Gene Regulation, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Koji HisatakeLaboratory of Gene Regulation, University of Tsukuba, Tsukuba, Ibaraki, Japan.
University of Tsukuba · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Gene ExpressionMolecular ImagingAdipocytes, BeigeAnimalsCell LineGene TargetingGenetic LociGenotypeHumansLuminescent ProteinsMiceMice, KnockoutMice, TransgenicRed Fluorescent ProteinSpectroscopy, Near-InfraredUncoupling Protein 1Luminescent ProteinsRed Fluorescent ProteinUCP1 protein, humanUncoupling Protein 1

Identifiers

PMID31730675
PMCPMC6857924
OpenAlexW2989344078

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.