Evidence map›Paper›PMID 25074913›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Zinc transporter SLC39A10/ZIP10 facilitates antiapoptotic signaling during early B-cell development.

Tomohiro Miyai, Shintaro Hojyo, Tomokatsu Ikawa, Masami Kawamura, Tarou Irié, Hideki Ogura, Atsushi Hijikata, Bum-Ho Bin, Takuwa Yasuda, Hiroshi Kitamura and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

84 citing papers in PubMed, 151 citations in OpenAlex.

  1. Article
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  5. Review
  6. Kynurenine-AhR-SLC39A10-ZnCell communication and signaling : CCS · 2026
    Article
  7. Article
  8. The role of metal ions iron, copper, and zinc in the immune microenvironment of gastric cancer.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2026
    Review
  9. Article
  10. Nutrigenomic profiling identifies ZIP10 (Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  11. Article
  12. ZIP3 is essential for the encephalitogenic function of pTh17 cells by regulating intracellular zinc levels.Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS) · 2026
    Article
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  15. Review
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  18. Article
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24 more citing papers are in PubMed but not listed here.

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

16 authors at 9 institutions in 4 countries.

Tomohiro MiyaiLaboratory for Immune Regeneration,Graduate School of Frontier Biosciences, Osaka University, Yamada-oka, Suita, Osaka 565-0871, Japan;
Shintaro HojyoLaboratory for Homeostatic Network,Osteoimmunology, Deutsches Rheuma-Forschungszentrum, Berlin, Charitéplatz, 10117 Berlin, Germany;
Tomokatsu IkawaLaboratory for Immune Regeneration.
Masami KawamuraLaboratory for Immunotherapy.
Tarou IriéDivision of Pathology, Department of Oral Diagnostic Sciences, School of Dentistry, Showa University, Hatanodai, Shinagawa, Tokyo 142-8555, Japan;
Hideki OguraLaboratory of Developmental Immunology, Graduate School of Medicine.
Atsushi HijikataNagahama Institute of Bio-Science and Technology, Tamura, Nagahama, Shiga 526-0829, Japan;
Bum-Ho BinDivision of Pathology, Department of Oral Diagnostic Sciences, School of Dentistry, Showa University, Hatanodai, Shinagawa, Tokyo 142-8555, Japan;Bioscience Research Institute, Amorepacific Corporation R&D Center, Yongin 446-729, Republic of Korea;
Takuwa YasudaLaboratory for Immunogenetics.
Hiroshi KitamuraDepartment of Veterinary Physiology, School of Veterinary Medicine, Rakuno Gakuen University, Ebetsu, Hokkaido 069-8501, Japan; and.
Manabu NakayamaDepartment of Human Genome Research, Kazusa DNA Research Institute, Kazusa-kamatari, Kisarazu, Chiba 292-0818, Japan.
Osamu OharaDepartment of Human Genome Research, Kazusa DNA Research Institute, Kazusa-kamatari, Kisarazu, Chiba 292-0818, JapanLaboratory for Integrative Genomics, and.
Hisahiro YoshidaLaboratory for Immunogenetics.
Haruhiko KosekiLaboratory for Developmental Genetics, RIKEN Center for Integrative Medical Sciences, Suehiro, Tsurumi, Yokohama, Kanagawa 230-0045, Japan;
Kenji MishimaDivision of Pathology, Department of Oral Diagnostic Sciences, School of Dentistry, Showa University, Hatanodai, Shinagawa, Tokyo 142-8555, Japan;
Toshiyuki FukadaLaboratory for Homeostatic Network,Division of Pathology, Department of Oral Diagnostic Sciences, School of Dentistry, Showa University, Hatanodai, Shinagawa, Tokyo 142-8555, Japan; fukada@rcai.riken.jp.
Showa University · JPImmungenetics (Germany) · DEKazusa DNA Research Institute · JPCharité - Universitätsmedizin Berlin · DELaboratory of Molecular Genetics · PLNagahama Institute of Bio-Science and Technology · JPOsaka University · JPRakuno Gakuen University · JPRIKEN Center for Integrative Medical Sciences · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The immune system is influenced by the vital zinc (Zn) status, and Zn deficiency triggers lymphopenia; however, the mechanisms underlying Zn-mediated lymphocyte maintenance remain elusive. Here we investigated ZIP10, a Zn transporter expressed in the early B-cell developmental process. Genetic ablation of Zip10 in early B-cell stages resulted in significant reductions in B-cell populations, and the inducible deletion of Zip10 in pro-B cells increased the caspase activity in parallel with a decrease in intracellular Zn levels. Similarly, the depletion of intracellular Zn by a chemical chelator resulted in spontaneous caspase activation leading to cell death. Collectively, these findings indicated that ZIP10-mediated Zn homeostasis is essential for early B-cell survival. Moreover, we found that ZIP10 expression was regulated by JAK-STAT pathways, and its expression was correlated with STAT activation in human B-cell lymphoma, indicating that the JAK-STAT-ZIP10-Zn signaling axis influences the B-cell homeostasis. Our results establish a role of ZIP10 in cell survival during early B-cell development, and underscore the importance of Zn homeostasis in immune system maintenance.

Indexed as

AnimalsApoptosisB-LymphocytesCaspasesCation Transport ProteinsCell DifferentiationCell SurvivalCytokinesHomeostasisHumansJanus KinasesLymphoma, B-CellLymphopeniaMiceMice, KnockoutModels, ImmunologicalCaspasesCation Transport ProteinsCytokinesJanus KinasesSLC39A10 protein, humanSTAT Transcription FactorsZincZIP10 protein, mouseapoptosisB-lymphocytebone marrowcytokinezinc-signaling axis

Identifiers

PMID25074913
PMCPMC4136617
OpenAlexW2001954481

What OpenQuestion holds

Textmetadata
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.