Evidence map›Paper›PMID 28854265›Full record

ArticlePLoS genetics2017

Zinc transporter ZIP13 suppresses beige adipocyte biogenesis and energy expenditure by regulating C/EBP-β expression.

Ayako Fukunaka, Toshiyuki Fukada, Jinhyuk Bhin, Luka Suzuki, Takamasa Tsuzuki, Yuri Takamine, Bum-Ho Bin, Toshinori Yoshihara, Noriko Ichinoseki-Sekine, Hisashi Naito and 8 more

Abstract read
In one paragraph

Article in PLoS genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

38 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
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  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Zinc homeostasis and redox alterations in obesity.Frontiers in endocrinology · 2023
    Review
  13. Zinc and Zinc Transporters in Dermatology.International journal of molecular sciences · 2022
    Review
  14. Review
  15. Article
  16. Nitric Oxide Mobilizes Intracellular ZnInternational journal of molecular sciences · 2022
    Article
  17. Article
  18. Article
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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

18 authors.

Ayako FukunakaDepartment of Metabolism & Endocrinology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Toshiyuki FukadaFaculty of Pharmaceutical Sciences, Tokushima Bunri University, Tokushima, Japan.
Jinhyuk BhinDepartment of Molecular Carcinogenesis, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Luka SuzukiDepartment of Metabolism & Endocrinology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Takamasa TsuzukiGraduate School of Health and Sports Science, Juntendo University, Inzai, Chiba, Japan.
Yuri TakamineGraduate School of Health and Sports Science, Juntendo University, Inzai, Chiba, Japan.
Bum-Ho BinDivision of Pathology, Department of Oral Diagnostic Sciences, School of Dentistry, Showa University, Tokyo, Japan.
Toshinori YoshiharaGraduate School of Health and Sports Science, Juntendo University, Inzai, Chiba, Japan.ORCID http://orcid.org/0000-0002-8465-5439
Noriko Ichinoseki-SekineGraduate School of Health and Sports Science, Juntendo University, Inzai, Chiba, Japan.ORCID http://orcid.org/0000-0002-0467-3312
Hisashi NaitoGraduate School of Health and Sports Science, Juntendo University, Inzai, Chiba, Japan.
Takeshi MiyatsukaDepartment of Metabolism & Endocrinology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Shinzaburo TakamiyaDepartment of Tropical Medicine and Parasitology, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
Tsutomu SasakiLaboratory of Metabolic Signaling, Institute for Molecular & Cellular Regulation, Gunma University, Maebashi, Gunma, Japan.
Takeshi InagakiLaboratory of Epigenetics and Metabolism, Institute for Molecular & Cellular Regulation, Gunma University, Maebashi, Gunma, Japan.
Tadahiro KitamuraLaboratory of Metabolic Signaling, Institute for Molecular & Cellular Regulation, Gunma University, Maebashi, Gunma, Japan.
Shingo KajimuraUCSF Diabetes Center and Department of Cell and Tissue Biology, University of California-San Francisco, San Francisco, United States of America.
Hirotaka WatadaDepartment of Metabolism & Endocrinology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Yoshio FujitaniDepartment of Metabolism & Endocrinology, Juntendo University Graduate School of Medicine, Tokyo, Japan.ORCID http://orcid.org/0000-0003-0196-4736

Funding

Research BaseP30DK063720 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GERMAN, MICHAEL S · 2003 to 2019
$21.8M
UCSF Nutrition Obesity Research CenterP30DK098722 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHRISTIAN VAISSE · 2015 to 2026
$14.6M
Molecular mechanisms of UCP1-independent pathways in metabolic healthR01DK097441 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Shingo Kajimura · 2012 to 2026
$5.9M
NIDDK NIH HHS P30 DK063720NIDDK NIH HHS P30 DK098722NIDDK NIH HHS R01 DK097441
6 · The paper itself

Abstract

Given the relevance of beige adipocytes in adult humans, a better understanding of the molecular circuits involved in beige adipocyte biogenesis has provided new insight into human brown adipocyte biology. Genetic mutations in SLC39A13/ZIP13, a member of zinc transporter family, are known to reduce adipose tissue mass in humans; however, the underlying mechanisms remains unknown. Here, we demonstrate that the Zip13-deficient mouse shows enhanced beige adipocyte biogenesis and energy expenditure, and shows ameliorated diet-induced obesity and insulin resistance. Both gain- and loss-of-function studies showed that an accumulation of the CCAAT/enhancer binding protein-β (C/EBP-β) protein, which cooperates with dominant transcriptional co-regulator PR domain containing 16 (PRDM16) to determine brown/beige adipocyte lineage, is essential for the enhanced adipocyte browning caused by the loss of ZIP13. Furthermore, ZIP13-mediated zinc transport is a prerequisite for degrading the C/EBP-β protein to inhibit adipocyte browning. Thus, our data reveal an unexpected association between zinc homeostasis and beige adipocyte biogenesis, which may contribute significantly to the development of new therapies for obesity and metabolic syndrome.

Indexed as

Adipocytes, BeigeAdipogenesisAnimalsCation Transport ProteinsCCAAT-Enhancer-Binding Protein-betaCell LineageDiet, High-FatDNA-Binding ProteinsEnergy MetabolismHumansInsulin ResistanceMiceMice, KnockoutObesityTranscription FactorsZincCation Transport ProteinsCCAAT-Enhancer-Binding Protein-betaCebpb protein, mouseDNA-Binding ProteinsPrdm16 protein, mouseSlc39a13 protein, mouseTranscription FactorsZinc

Identifiers

PMID28854265
PMCPMC5576661

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.