Evidence map›Paper›PMID 27234056›Full record

ArticleImmunity2016

Fine-Tuning of CD8(+) T Cell Mitochondrial Metabolism by the Respiratory Chain Repressor MCJ Dictates Protection to Influenza Virus.

Devin P Champagne, Ketki M Hatle, Karen A Fortner, Angelo D'Alessandro, Tina M Thornton, Rui Yang, Daniel Torralba, Julen Tomás-Cortázar, Yong Woong Jun, Kyo Han Ahn and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
9.6field-weighted citation impact, top 2% 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

44 citing papers in PubMed, 71 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. High-Throughput Metabolomics in Transfusion Medicine.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  6. Review
  7. Review
  8. Immunometabolic Maladaptations to the Tumor Microenvironment.Cold Spring Harbor perspectives in medicine · 2024
    Review
  9. Oligonucleotide therapies for nonalcoholic steatohepatitis.Molecular therapy. Nucleic acids · 2024
    Review
  10. Article
  11. Unveiling the mechanisms and challenges of cancer drug resistance.Cell communication and signaling : CCS · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Targeting memory T cell metabolism to improve immunity.The Journal of clinical investigation · 2022
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 6 institutions in 3 countries.

Devin P ChampagneProgram in Immunobiology, Department of Medicine, University of Vermont, Burlington, Vermont, 05405 USA.
Ketki M HatleProgram in Immunobiology, Department of Medicine, University of Vermont, Burlington, Vermont, 05405 USA.
Karen A FortnerProgram in Immunobiology, Department of Medicine, University of Vermont, Burlington, Vermont, 05405 USA.
Angelo D'AlessandroDepartment of Biochemistry and Molecular Genetics, University of Colorado Denver, Aurora, CO 80045, USA.
Tina M ThorntonProgram in Immunobiology, Department of Medicine, University of Vermont, Burlington, Vermont, 05405 USA.
Rui YangProgram in Immunobiology, Department of Medicine, University of Vermont, Burlington, Vermont, 05405 USA.
Daniel TorralbaProgram in Immunobiology, Department of Medicine, University of Vermont, Burlington, Vermont, 05405 USA.
Julen Tomás-CortázarCenter for Cooperative Research in Biosciences (CIC bioGUNE), Derio 48160 Bizkaia, Spain.
Yong Woong JunDepartment of Chemistry, Center for Electro-Photo Behaviors in Advanced Molecular Systems, Pohang University of Science and Technology (POSTECH), Nam-Gu, Pohang, 790-784 Gyeongbuk, Republic of Korea.
Kyo Han AhnDepartment of Chemistry, Center for Electro-Photo Behaviors in Advanced Molecular Systems, Pohang University of Science and Technology (POSTECH), Nam-Gu, Pohang, 790-784 Gyeongbuk, Republic of Korea.
Kirk C HansenDepartment of Biochemistry and Molecular Genetics, University of Colorado Denver, Aurora, CO 80045, USA.
Laura HaynesCenter on Aging and Department of Immunology, University of Connecticut Health Center, Farmington, CT 06030 USA.
Juan AnguitaCenter for Cooperative Research in Biosciences (CIC bioGUNE), Derio 48160 Bizkaia, Spain; Ikerbasque, Basque Foundation for Science, Bilbao, Bizkaia, Spain.
Mercedes RinconProgram in Immunobiology, Department of Medicine, University of Vermont, Burlington, Vermont, 05405 USA. Electronic address: mrincon@uvm.edu.
University of Vermont · USPohang University of Science and Technology · KRUniversity of Colorado Denver · USCIC bioGUNE · ESIkerbasque · ESUConn Health · US

Funding

Vermont Immunobioloigy/ Infectious Diseases CenterP20GM103496 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI BUDD, RALPH C · 2012 to 2015
$8.7M
Vermont Immunology/Infectious Diseases Training GrantT32AI055402 · NIAID · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI GARY E WARD · 2005 to 2026
$2.7M
Regulation of mitochondrial function in T cellsR21AI110016 · NIAID · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI RINCON, MERCEDES · 2014 to 2015
$419k
Upgrade of a FACS Aria Cell SorterS10OD018175 · OD · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI BOYSON, JONATHAN E · 2015 to 2015
$153k
NIAID NIH HHS R21 AI110016NIAID NIH HHS T32 AI055402NIGMS NIH HHS P20 GM103496NIH HHS S10 OD018175
6 · The paper itself

Abstract

Mitochondrial respiration is regulated in CD8(+) T cells during the transition from naive to effector and memory cells, but mechanisms controlling this process have not been defined. Here we show that MCJ (methylation-controlled J protein) acted as an endogenous break for mitochondrial respiration in CD8(+) T cells by interfering with the formation of electron transport chain respiratory supercomplexes. Metabolic profiling revealed enhanced mitochondrial metabolism in MCJ-deficient CD8(+) T cells. Increased oxidative phosphorylation and subcellular ATP accumulation caused by MCJ deficiency selectively increased the secretion, but not expression, of interferon-γ. MCJ also adapted effector CD8(+) T cell metabolism during the contraction phase. Consequently, memory CD8(+) T cells lacking MCJ provided superior protection against influenza virus infection. Thus, MCJ offers a mechanism for fine-tuning CD8(+) T cell mitochondrial metabolism as an alternative to modulating mitochondrial mass, an energetically expensive process. MCJ could be a therapeutic target to enhance CD8(+) T cell responses.

Indexed as

Adenosine TriphosphateAnimalsCD8-Positive T-LymphocytesCell RespirationCells, CulturedElectron Transport Chain Complex ProteinsImmunologic MemoryInterferon-gammaLymphocyte ActivationMetabolomeMiceMice, Inbred C57BLMice, KnockoutMitochondriaMitochondrial ProteinsMolecular ChaperonesAdenosine TriphosphateElectron Transport Chain Complex ProteinsInterferon-gammaMcj protein, mouseMitochondrial ProteinsMolecular Chaperones

Identifiers

PMID27234056
PMCPMC4917451
OpenAlexW2407406296

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.