Evidence map›Paper›PMID 34880245›Full record

ArticleNature communications2021

Free fatty-acid transport via CD36 drives β-oxidation-mediated hematopoietic stem cell response to infection.

Jayna J Mistry, Charlotte Hellmich, Jamie A Moore, Aisha Jibril, Iain Macaulay, Mar Moreno-Gonzalez, Federica Di Palma, Naiara Beraza, Kristian M Bowles, Stuart A Rushworth

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 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
8.8field-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

57 citing papers in PubMed, 114 citations in OpenAlex.

  1. Article
  2. Hematopoietic Stem Cell Metabolism during Stress and Aging.Advances in geriatric medicine and research · 2026
    Article
  3. Estivation Strategies of Invasive SnailEcology and evolution · 2026
    Article
  4. Article
  5. Article
  6. Review
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  8. Article
  9. Article
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  11. Review
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  14. Article
  15. Review
  16. Review
  17. Review
  18. Lipid Metabolism and Immune Function: Chemical Tools for Insights into T-Cell Biology.Chembiochem : a European journal of chemical biology · 2025
    Review
  19. Review
  20. Hematopoietic stem cell metabolism within the bone marrow niche - insights and opportunities.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
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

10 authors at 3 institutions in 1 country.

Jayna J MistryNorwich Medical School, University of East Anglia, Norwich Research Park, Norwich, NR4 7UQ, UK.
Charlotte HellmichNorwich Medical School, University of East Anglia, Norwich Research Park, Norwich, NR4 7UQ, UK.
Jamie A MooreNorwich Medical School, University of East Anglia, Norwich Research Park, Norwich, NR4 7UQ, UK.
Aisha JibrilNorwich Medical School, University of East Anglia, Norwich Research Park, Norwich, NR4 7UQ, UK.
Iain MacaulayEarlham Institute, Norwich Research Park, Norwich, NR4 7UH, UK.
Mar Moreno-GonzalezGut Microbes and Health Institute Strategic Programme, Quadram Institute, Norwich, UK.ORCID http://orcid.org/0000-0002-5840-5751
Federica Di PalmaNorwich Medical School, University of East Anglia, Norwich Research Park, Norwich, NR4 7UQ, UK.
Naiara BerazaGut Microbes and Health Institute Strategic Programme, Quadram Institute, Norwich, UK. naiara.beraza@quadram.ac.uk.
Kristian M BowlesNorwich Medical School, University of East Anglia, Norwich Research Park, Norwich, NR4 7UQ, UK. k.bowles@uea.ac.uk.ORCID http://orcid.org/0000-0003-1334-4526
Stuart A RushworthNorwich Medical School, University of East Anglia, Norwich Research Park, Norwich, NR4 7UQ, UK. s.rushworth@uea.ac.uk.ORCID http://orcid.org/0000-0002-3711-7558
University of East Anglia · GBQuadram Institute · GBNorwich Research Park · GB

Funding

Biotechnology and Biological Sciences Research Council BBS/E/T/000PR9816Medical Research Council MR/T02934X/1Wellcome Trust
6 · The paper itself

Abstract

Acute infection is known to induce rapid expansion of hematopoietic stem cells (HSCs), but the mechanisms supporting this expansion remain incomplete. Using mouse models, we show that inducible CD36 is required for free fatty acid uptake by HSCs during acute infection, allowing the metabolic transition from glycolysis towards β-oxidation. Mechanistically, high CD36 levels promote FFA uptake, which enables CPT1A to transport fatty acyl chains from the cytosol into the mitochondria. Without CD36-mediated FFA uptake, the HSCs are unable to enter the cell cycle, subsequently enhancing mortality in response to bacterial infection. These findings enhance our understanding of HSC metabolism in the bone marrow microenvironment, which supports the expansion of HSCs during pathogenic challenge.

Indexed as

AnimalsBone MarrowCD36 AntigensCell CycleFatty AcidsFatty Acids, NonesterifiedGlycolysisHematopoietic Stem CellsHost Microbial InteractionsLipopolysaccharidesMiceMice, Inbred C57BLMitochondriaOxidation-ReductionSalmonella InfectionsSalmonella typhimuriumCD36 AntigensCd36 protein, mouseFatty AcidsFatty Acids, NonesterifiedLipopolysaccharides

Identifiers

PMID34880245
PMCPMC8655073
OpenAlexW4200304704

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.