Evidence map›Paper›PMID 39675714›Full record

ArticleThe Journal of biological chemistry2025

Phase partitioning of the neutrophil oxidative burst is coordinated by accessory pathways of glucose metabolism and mitochondrial activity.

Tyler Jobe, Jonah Stephan, Collin K Wells, Maleesha De Silva, Pawel K Lorkiewicz, Bradford G Hill, Marcin Wysoczynski

Abstract read
In one paragraph

Article in The Journal of biological chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. O-GlcNAc informatics: advances and trends.Analytical and bioanalytical chemistry · 2025
    Review
  8. 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

7 authors.

Tyler JobeCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, University of Louisville, Louisville, Kentucky; Department of Physiology, School of Medicine, University of Louisville, Louisville, Kentucky.
Jonah StephanCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, University of Louisville, Louisville, Kentucky; Department of Biochemistry, School of Medicine, University of Louisville, Louisville, Kentucky.
Collin K WellsCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, University of Louisville, Louisville, Kentucky; Department of Biochemistry, School of Medicine, University of Louisville, Louisville, Kentucky.
Maleesha De SilvaCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, University of Louisville, Louisville, Kentucky.
Pawel K LorkiewiczCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, University of Louisville, Louisville, Kentucky.
Bradford G HillCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, University of Louisville, Louisville, Kentucky. Electronic address: bradford.hill@louisville.edu.
Marcin WysoczynskiCenter for Cardiometabolic Science, Christina Lee Brown Envirome Institute, University of Louisville, Louisville, Kentucky. Electronic address: m0wyso01@louisville.edu.

Funding

TBDP30GM127607 · NIGMS · UNIVERSITY OF LOUISVILLE · PI BHATNAGAR, ARUNI · 2018 to 2022
$6.3M
Role of the PEP cycle in cardiac fibrosisR01HL168198 · NHLBI · UNIVERSITY OF LOUISVILLE · PI Bradford Guy Hill · 2024 to 2026
$1.7M
Bruker timsTOF Mass SpectrometerS10OD026840 · OD · UNIVERSITY OF LOUISVILLE · PI LORKIEWICZ, PAWEL K · 2020 to 2020
$598k
NHLBI NIH HHS R01 HL168198NIGMS NIH HHS P30 GM127607NIH HHS S10 OD026840
6 · The paper itself

Abstract

Neutrophils are a part of the innate immune system and produce reactive oxygen species (ROS) to extinguish pathogens. The major source of ROS in neutrophils is NADPH oxidase, which is fueled by NADPH generated via the pentose phosphate pathway; however, it is unclear how other accessory glucose metabolism pathways and mitochondrial activity influence the respiratory burst. We examined the temporal dynamics of the respiratory burst and delineated how metabolism changes over time after neutrophil activation. Bone marrow-derived neutrophils were stimulated with phorbol 12-myristate 13-acetate, and the respiratory burst was measured via extracellular flux analysis. Metabolomics experiments utilizing

Indexed as

GlucoseMitochondriaNeutrophilsRespiratory BurstAnimalsGlycolysisMiceReactive Oxygen SpeciesTetradecanoylphorbol AcetateGlucoseReactive Oxygen SpeciesTetradecanoylphorbol Acetateglycolysisinnate immunitymitochondriapathogenreactive oxygen species

Identifiers

PMID39675714
PMCPMC11760813

What OpenQuestion holds

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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.