Evidence map›Paper›PMID 24145050›Full record

ArticleBrain, behavior, and immunity2014

Cell-autonomous iodothyronine deiodinase expression mediates seasonal plasticity in immune function.

Tyler J Stevenson, Kenneth G Onishi, Sean P Bradley, Brian J Prendergast

Abstract read
In one paragraph

Article in Brain, behavior, and immunity, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
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  3. Article
  4. Endocrine and molecular regulation of seasonal avian immune function.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  5. Article
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  7. Article
  8. Genome sequencing and transcriptome analyses of the Siberian hamster hypothalamus identify mechanisms for seasonal energy balance.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
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  10. Review
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  12. Article
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  14. Review
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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

4 authors at 1 institution in 1 country.

Tyler J StevensonInstitute for Mind and Biology, University of Chicago, Chicago, IL 60637, USA. Electronic address: tyler.stevenson@abdn.ac.uk.
Kenneth G OnishiInstitute for Mind and Biology, University of Chicago, Chicago, IL 60637, USA.
Sean P BradleyInstitute for Mind and Biology, University of Chicago, Chicago, IL 60637, USA; Department of Psychology, University of Chicago, Chicago, IL 60637, USA.
Brian J PrendergastInstitute for Mind and Biology, University of Chicago, Chicago, IL 60637, USA; Department of Psychology, University of Chicago, Chicago, IL 60637, USA.
University of Chicago · US

Funding

Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
Processing Photoperiod Information by the Immune SystemR01AI067406 · NIAID · UNIVERSITY OF CHICAGO · PI PRENDERGAST, BRIAN J · 2005 to 2015
$3.2M
NCATS NIH HHS UL1 TR000430NIAID NIH HHS AI-67406NIAID NIH HHS R01 AI067406
6 · The paper itself

Abstract

Annual rhythms in morbidity and mortality are well-documented, and host defense mechanisms undergo marked seasonal phenotypic change. Siberian hamsters (Phodopus sungorus) exhibit striking immunological plasticity following adaptation to short winter day lengths (SD), including increases in blood leukocytes and in the magnitude of T cell-mediated immune responses. Thyroid hormone (TH) signaling is rate-limited by tissue-level expression of iodothyronine deiodinase types II and III (dio2, dio3), and dio2/dio3 expression in the central nervous system gate TH-dependent transduction of photoperiod information into the neuroendocrine system. THs are also potent immunomodulators, but their role in seasonal immunobiology remains unexamined. Here we report that photoperiod-driven changes in triiodothyronine (T3) signaling mediate seasonal changes in multiple aspects of immune function. Transfer from long days (LD) to SD inhibited leukocyte dio3 expression, which increased cellular T4→T3 catabolism. T3 was preferentially localized in the lymphocyte cytoplasm, consistent with a non-nuclear role of T3 in lymphoid cell differentiation and maturation. Exposure to SD upregulated leukocyte DNA methyltransferase expression and markedly increased DNA methylation in the dio3 proximal promoter region. Lastly, to bypass low endogenous T3 biosynthesis in LD lymphocytes, LD hamsters were treated with T3, which enhanced T cell-dependent delayed-type hypersensitivity inflammatory responses and blood leukocyte concentrations in a dose-dependent manner, mimicking effects of SD on these immunophenotypes. T3 signaling represents a novel mechanism by which environmental day length cues impact the immune system: changes in day length alter lymphoid cell T3-signaling via epigenetic transcriptional control of dio3 expression.

Indexed as

AnimalsCircadian RhythmCricetinaeDNA MethylationFemaleIodide PeroxidaseLeukocytesMalePhodopusPhotoperiodSeasonsThyroxineTriiodothyronineIodide PeroxidaseThyroxineTriiodothyronineAdaptive immunityCytometryHamsterImaging flow cytometryPhotoperiodRhythmThyroid

Identifiers

PMID24145050
PMCPMC3974869
OpenAlexW2004776011

What OpenQuestion holds

Textmetadata
LicenceTDM
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.