Evidence map›Paper›PMID 30580967›Full record

ArticleMolecular metabolism2019

A dual Ucp1 reporter mouse model for imaging and quantitation of brown and brite fat recruitment.

Hui Wang, Monja Willershäuser, Angelos Karlas, Dimitris Gorpas, Josefine Reber, Vasilis Ntziachristos, Stefanie Maurer, Tobias Fromme, Yongguo Li, Martin Klingenspor

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

28 citing papers in PubMed, 48 citations in OpenAlex.

  1. Brown Adipose Tissue in Breast Cancer Evaluated by [Molecular imaging and biology · 2020
    Trial
  2. Article
  3. Review
  4. Article
  5. Review
  6. No UCP1 in the kidney.Molecular metabolism · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Development and expansion of intramuscular adipose tissue is not dependent on UCP-1-lineage cells in mice.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2023
    Article
  11. Review
  12. Uncoupling protein 1-driven Cre (bioRxiv : the preprint server for biology · 2023
    Article
  13. The widely usedbioRxiv : the preprint server for biology · 2023
    Article
  14. Article
  15. Article
  16. Visualization and quantification ofAnnals of translational medicine · 2022
    Article
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  18. Review
  19. Article
  20. 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 3 institutions in 1 country.

Hui WangEKFZ - Else Kröner-Fresenius Zentrum for Nutritional Medicine, Technical University of Munich, Gregor-Mendel-Str. 2, 85354 Freising, Germany; Chair for Molecular Nutritional Medicine, Technical University of Munich, Gregor-Mendel-Str. 2, 85354 Freising, Germany.
Monja WillershäuserEKFZ - Else Kröner-Fresenius Zentrum for Nutritional Medicine, Technical University of Munich, Gregor-Mendel-Str. 2, 85354 Freising, Germany; Chair for Molecular Nutritional Medicine, Technical University of Munich, Gregor-Mendel-Str. 2, 85354 Freising, Germany.
Angelos KarlasChair for Biological Imaging, Technical University of Munich, Troger Str. 9, 81675 München, Germany.
Dimitris GorpasInstitute for Biological and Medical Imaging (IBMI), Helmholtz Zentrum München, Ingolstädter Landstr.1, 85764 Neuherberg, Germany; Chair for Biological Imaging, Technical University of Munich, Troger Str. 9, 81675 München, Germany.
Josefine ReberInstitute for Biological and Medical Imaging (IBMI), Helmholtz Zentrum München, Ingolstädter Landstr.1, 85764 Neuherberg, Germany.
Vasilis NtziachristosInstitute for Biological and Medical Imaging (IBMI), Helmholtz Zentrum München, Ingolstädter Landstr.1, 85764 Neuherberg, Germany; Chair for Biological Imaging, Technical University of Munich, Troger Str. 9, 81675 München, Germany.
Stefanie MaurerEKFZ - Else Kröner-Fresenius Zentrum for Nutritional Medicine, Technical University of Munich, Gregor-Mendel-Str. 2, 85354 Freising, Germany; Chair for Molecular Nutritional Medicine, Technical University of Munich, Gregor-Mendel-Str. 2, 85354 Freising, Germany.
Tobias FrommeEKFZ - Else Kröner-Fresenius Zentrum for Nutritional Medicine, Technical University of Munich, Gregor-Mendel-Str. 2, 85354 Freising, Germany; Chair for Molecular Nutritional Medicine, Technical University of Munich, Gregor-Mendel-Str. 2, 85354 Freising, Germany.
Yongguo LiEKFZ - Else Kröner-Fresenius Zentrum for Nutritional Medicine, Technical University of Munich, Gregor-Mendel-Str. 2, 85354 Freising, Germany; Chair for Molecular Nutritional Medicine, Technical University of Munich, Gregor-Mendel-Str. 2, 85354 Freising, Germany.
Martin KlingensporEKFZ - Else Kröner-Fresenius Zentrum for Nutritional Medicine, Technical University of Munich, Gregor-Mendel-Str. 2, 85354 Freising, Germany; Chair for Molecular Nutritional Medicine, Technical University of Munich, Gregor-Mendel-Str. 2, 85354 Freising, Germany. Electronic address: mk@tum.de.
Fresenius (Germany) · DEHelmholtz Zentrum München · DETechnical University of Munich · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesBrown adipose tissue (BAT) dissipates nutritional energy as heat through uncoupling protein 1 (UCP1). The discovery of functional BAT in healthy adult humans has promoted the search for pharmacological interventions to recruit and activate brown fat as a treatment of obesity and diabetes type II. These efforts require in vivo models to compare the efficacy of novel compounds in a relevant physiological context.

methodsWe generated a knock-in mouse line expressing firefly luciferase and near-infrared red florescent protein (iRFP713) driven by the regulatory elements of the endogenous Ucp1 gene.

resultsOur detailed characterization revealed that firefly luciferase activity faithfully reports endogenous Ucp1 gene expression in response to physiological and pharmacological stimuli. The iRFP713 fluorescence signal was detected in the interscapular BAT region of cold-exposed reporter mice in an allele-dosage dependent manner. Using this reporter mouse model, we detected a higher browning capacity in female peri-ovarian white adipose tissue compared to male epididymal WAT, which we further corroborated by molecular and morphological features. In situ imaging detected a strong luciferase activity signal in a previously unappreciated adipose tissue depot adjunct to the femoral muscle, now adopted as femoral brown adipose tissue. In addition, screening cultured adipocytes by bioluminescence imaging identified the selective Salt-Inducible Kinase inhibitor, HG-9-91-01, to increase Ucp1 gene expression and mitochondrial respiration in brown and brite adipocytes.

conclusionsIn our mouse model, firefly luciferase activity serves as a bona fide reporter for dynamic regulation of Ucp1. In addition, by means of iRFP713 we are able to monitor Ucp1 expression in a non-invasive fashion.

Indexed as

Genes, ReporterThermogenesisAdipose Tissue, BeigeAdipose Tissue, BrownAnimalsCell LineCells, CulturedLuciferases, FireflyLuminescent ProteinsMiceMice, Inbred C57BLRed Fluorescent ProteinUncoupling Protein 1Luciferases, FireflyLuminescent ProteinsRed Fluorescent ProteinUcp1 protein, mouseUncoupling Protein 1BATBrowningFirefly luciferaseiRFP713ThermogenesisUCP1WAT

Identifiers

PMID30580967
PMCPMC6358570
OpenAlexW2902358898

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.