Evidence map›Paper›PMID 33822765›Full record

ArticleThe Journal of clinical investigation2021

Hypoxia drives murine neutrophil protein scavenging to maintain central carbon metabolism.

Emily R Watts, Andrew Jm Howden, Tyler Morrison, Pranvera Sadiku, Jens Hukelmann, Alex von Kriegsheim, Bart Ghesquiere, Fiona Murphy, Ananda S Mirchandani, Duncan C Humphries and 11 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

31 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Multi‑omics reveal neutrophil heterogeneity in sepsis (Review).International journal of molecular medicine · 2025
    Review
  5. Article
  6. Pleiotropic Mucosal Innate Immune Memory in the Gastrointestinal Tract.International journal of molecular sciences · 2025
    Review
  7. Review
  8. [Advancement in neutrophil-based drug delivery systems].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2025
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Nanoparticle targeting of neutrophil glycolysis prevents lung ischemia-reperfusion injury.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2024
    Article
  18. Article
  19. Observational
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 3 institutions in 1 country.

Emily R WattsUniversity of Edinburgh Centre for Inflammation Research, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom.
Andrew Jm HowdenDivision of Cell Signaling and Immunology, University of Dundee, Dundee, United Kingdom.
Tyler MorrisonUniversity of Edinburgh Centre for Inflammation Research, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom.
Pranvera SadikuUniversity of Edinburgh Centre for Inflammation Research, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom.
Jens HukelmannDivision of Cell Signaling and Immunology, University of Dundee, Dundee, United Kingdom.
Alex von KriegsheimEdinburgh Cancer Research Centre, IGMM, University of Edinburgh, Edinburgh, United Kingdom.
Bart GhesquiereLaboratory of Angiogenesis and Vascular Metabolism, Vesalius Research Centre, Leuven, Belgium.
Fiona MurphyUniversity of Edinburgh Centre for Inflammation Research, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom.
Ananda S MirchandaniUniversity of Edinburgh Centre for Inflammation Research, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom.
Duncan C HumphriesUniversity of Edinburgh Centre for Inflammation Research, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom.
Robert GrecianUniversity of Edinburgh Centre for Inflammation Research, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom.
Eilise M RyanUniversity of Edinburgh Centre for Inflammation Research, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom.
Patricia CoelhoUniversity of Edinburgh Centre for Inflammation Research, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom.
Gio Rodriguez BlancoEdinburgh Cancer Research Centre, IGMM, University of Edinburgh, Edinburgh, United Kingdom.
Tracie M PlantUniversity of Edinburgh Centre for Inflammation Research, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom.
Rebecca S DickinsonUniversity of Edinburgh Centre for Inflammation Research, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom.
Andy FinchEdinburgh Cancer Research Centre, IGMM, University of Edinburgh, Edinburgh, United Kingdom.
Wesley VermaelenLaboratory of Angiogenesis and Vascular Metabolism, Vesalius Research Centre, Leuven, Belgium.
Doreen A CantrellDivision of Cell Signaling and Immunology, University of Dundee, Dundee, United Kingdom.
Moira K WhyteUniversity of Edinburgh Centre for Inflammation Research, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom.
Sarah R WalmsleyUniversity of Edinburgh Centre for Inflammation Research, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom.
Centre for Inflammation Research · GBEdinburgh Cancer Research · GBUniversity of Dundee · GB

Funding

Wellcome Trust 098516Wellcome Trust 108717/Z/15/ZWellcome Trust 110086/Z/15/ZWellcome Trust 205023/Z/16/ZWellcome Trust 209220Wellcome Trust 209220/Z/17/Z
6 · The paper itself

Abstract

Limiting dysfunctional neutrophilic inflammation while preserving effective immunity requires a better understanding of the processes that dictate neutrophil function in the tissues. Quantitative mass-spectrometry identified how inflammatory murine neutrophils regulated expression of cell surface receptors, signal transduction networks, and metabolic machinery to shape neutrophil phenotypes in response to hypoxia. Through the tracing of labeled amino acids into metabolic enzymes, proinflammatory mediators, and granule proteins, we demonstrated that ongoing protein synthesis shapes the neutrophil proteome. To maintain energy supplies in the tissues, neutrophils consumed extracellular proteins to fuel central carbon metabolism. The physiological stresses of hypoxia and hypoglycemia, characteristic of inflamed tissues, promoted this extracellular protein scavenging with activation of the lysosomal compartment, further driving exploitation of the protein-rich inflammatory milieu. This study provides a comprehensive map of neutrophil proteomes, analysis of which has led to the identification of active catabolic and anabolic pathways that enable neutrophils to sustain synthetic and effector functions in the tissues.

Indexed as

Protein BiosynthesisAnimalsCarbonCell HypoxiaHumansLysosomesMiceNeutrophilsProteomeCarbonProteomeHypoxiaInflammationMetabolismNeutrophilsProteomics

Identifiers

PMID33822765
PMCPMC8121528
OpenAlexW3140722450

What OpenQuestion holds

Textmetadata
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.