Evidence map›Paper›PMID 33619282›Full record

ArticleNature communications2021

Fructose reprogrammes glutamine-dependent oxidative metabolism to support LPS-induced inflammation.

Nicholas Jones, Julianna Blagih, Fabio Zani, April Rees, David G Hill, Benjamin J Jenkins, Caroline J Bull, Diana Moreira, Azari I M Bantan, James G Cronin and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed
18.8field-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

98 citing papers in PubMed, 171 citations in OpenAlex.

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  9. Microglial fructose metabolism is essential for glioblastoma growth.Proceedings of the National Academy of Sciences of the United States of America · 2026
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38 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 5 institutions in 3 countries.

Nicholas Jones *Institute of Life Science, Swansea University Medical School, Swansea University, Swansea, UK.ORCID 0000-0003-4846-5117
Julianna Blagih *The Francis Crick Institute, London, UK.
Fabio ZaniThe Francis Crick Institute, London, UK.
April ReesInstitute of Life Science, Swansea University Medical School, Swansea University, Swansea, UK.
David G HillCellular and Molecular Medicine, University of Bristol, Bristol, UK.
Benjamin J JenkinsInstitute of Life Science, Swansea University Medical School, Swansea University, Swansea, UK.
Caroline J BullCellular and Molecular Medicine, University of Bristol, Bristol, UK.ORCID 0000-0002-2176-5120
Diana MoreiraSchool of Biochemistry and Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin, Ireland.
Azari I M BantanInstitute of Life Science, Swansea University Medical School, Swansea University, Swansea, UK.
James G CroninInstitute of Life Science, Swansea University Medical School, Swansea University, Swansea, UK.ORCID 0000-0002-0590-9462
Daniele AvanciniSan Raffaele Telethon Institute for Gene Therapy, San Raffaele Scientific Institute, Milan, Italy.
Gareth W JonesCellular and Molecular Medicine, University of Bristol, Bristol, UK.ORCID 0000-0002-0125-4841
David K FinlaySchool of Biochemistry and Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin, Ireland.
Karen H VousdenThe Francis Crick Institute, London, UK.ORCID 0000-0002-7365-1766
Emma E VincentCellular and Molecular Medicine, University of Bristol, Bristol, UK. emma.vincent@bristol.ac.uk.ORCID 0000-0002-8917-7384
Catherine A ThorntonInstitute of Life Science, Swansea University Medical School, Swansea University, Swansea, UK. c.a.thornton@swansea.ac.uk.
Swansea University · GBUniversity of Bristol · GBThe Francis Crick Institute · GBTrinity College Dublin · IEThe San Raffaele Telethon Institute for Gene Therapy · IT

Funding

Cancer Research UK 29019Cancer Research UK C18281/A29019Cancer Research UK C596/A10419Cancer Research UK C596/A26855Cancer Research UK FC001557Medical Research Council FC001557Versus Arthritis 20305Versus Arthritis 22706Wellcome Trust FC001557
6 · The paper itself

Abstract

Fructose intake has increased substantially throughout the developed world and is associated with obesity, type 2 diabetes and non-alcoholic fatty liver disease. Currently, our understanding of the metabolic and mechanistic implications for immune cells, such as monocytes and macrophages, exposed to elevated levels of dietary fructose is limited. Here, we show that fructose reprograms cellular metabolic pathways to favour glutaminolysis and oxidative metabolism, which are required to support increased inflammatory cytokine production in both LPS-treated human monocytes and mouse macrophages. A fructose-dependent increase in mTORC1 activity drives translation of pro-inflammatory cytokines in response to LPS. LPS-stimulated monocytes treated with fructose rely heavily on oxidative metabolism and have reduced flexibility in response to both glycolytic and mitochondrial inhibition, suggesting glycolysis and oxidative metabolism are inextricably coupled in these cells. The physiological implications of fructose exposure are demonstrated in a model of LPS-induced systemic inflammation, with mice exposed to fructose having increased levels of circulating IL-1β after LPS challenge. Taken together, our work underpins a pro-inflammatory role for dietary fructose in LPS-stimulated mononuclear phagocytes which occurs at the expense of metabolic flexibility.

Indexed as

AcidsAnimalsCitric Acid CycleCytokinesDisease Models, AnimalFructoseGlucoseGlutamineGlycolysisInflammationIsotope LabelingLipopolysaccharidesMacrophagesMetabolic Flux AnalysisMiceMice, Inbred C57BLAcidsCytokinesFructoseGlucoseGlutamineLipopolysaccharides

Identifiers

PMID33619282
PMCPMC7900179
OpenAlexW3119836065

What OpenQuestion 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 OpenQuestion graph.