Evidence map›Paper›PMID 27111141›Full record

ArticleNature immunology2016

Glucose and glutamine fuel protein O-GlcNAcylation to control T cell self-renewal and malignancy.

Mahima Swamy, Shalini Pathak, Katarzyna M Grzes, Sebastian Damerow, Linda V Sinclair, Daan M F van Aalten, Doreen A Cantrell

Open access · greenAbstract read
In one paragraph

Article in Nature immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 230 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
230citing papers in PubMed, 2 pooled it
19.5field-weighted citation impact, top 1% 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

230 citing papers in PubMed, 2 syntheses or guidelines pooled it, 348 citations in OpenAlex.

  1. Pooled it
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  3. Article
  4. d-Sorbose Promotes Regulatory T-Cell Differentiation and Ameliorates Autoimmune and Allergic Diseases via Hexosamine Biosynthetic Pathway Inhibition.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  5. Review
  6. T Cell O-GlcNAcylation Increases in Patients With Allergic Rhinitis After the Natural Pollen Season.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2026
    Article
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170 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Mahima SwamyDivision of Cell Signalling and Immunology, University of Dundee, Dundee, UK.ORCID 0000-0003-3977-3425
Shalini PathakDivision of Cell Signalling and Immunology, University of Dundee, Dundee, UK.
Katarzyna M GrzesDivision of Cell Signalling and Immunology, University of Dundee, Dundee, UK.
Sebastian DamerowDivision of Biological Chemistry and Drug Discovery, University of Dundee, Dundee, UK.
Linda V SinclairDivision of Cell Signalling and Immunology, University of Dundee, Dundee, UK.
Daan M F van AaltenMedical Research Council Protein Phosphorylation and Ubiquitylation Unit, University of Dundee, Dundee, UK.ORCID 0000-0002-1499-6908
Doreen A CantrellDivision of Cell Signalling and Immunology, University of Dundee, Dundee, UK.
University of Dundee · GB

Funding

Wellcome Trust 097418
6 · The paper itself

Abstract

Sustained glucose and glutamine transport are essential for activated T lymphocytes to support ATP and macromolecule biosynthesis. We found that glutamine and glucose also fuel an indispensable dynamic regulation of intracellular protein O-GlcNAcylation at key stages of T cell development, transformation and differentiation. Glucose and glutamine are precursors of uridine diphosphate N-acetylglucosamine (UDP-GlcNAc), a substrate for cellular glycosyltransferases. Immune-activated T cells contained higher concentrations of UDP-GlcNAc and increased intracellular protein O-GlcNAcylation controlled by the enzyme O-linked-β-N-acetylglucosamine (O-GlcNAc) glycosyltransferase as compared with naive cells. We identified Notch, the T cell antigen receptor and c-Myc as key controllers of T cell protein O-GlcNAcylation via regulation of glucose and glutamine transport. Loss of O-GlcNAc transferase blocked T cell progenitor renewal, malignant transformation and peripheral T cell clonal expansion. Nutrient-dependent signaling pathways regulated by O-GlcNAc glycosyltransferase are thus fundamental for T cell biology.

Indexed as

AnimalsCell ProliferationCell Self RenewalCell Transformation, NeoplasticClone CellsFemaleGlucoseGlutamineLymphocyte ActivationLymphocyte Specific Protein Tyrosine Kinase p56(lck)MaleMiceMice, Inbred C57BLMice, KnockoutN-AcetylglucosaminyltransferasesProto-Oncogene Proteins c-mycGlucoseGlutamineLymphocyte Specific Protein Tyrosine Kinase p56(lck)Myc protein, mouseN-AcetylglucosaminyltransferasesProto-Oncogene Proteins c-mycReceptors, Antigen, T-CellReceptors, NotchUridine Diphosphate N-Acetylglucosamine

Identifiers

PMID27111141
PMCPMC4900450
OpenAlexW2343796589

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.