Evidence map›Paper›PMID 39284072›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Activation induces shift in nutrient utilization that differentially impacts cell functions in human neutrophils.

Emily C Britt, Xin Qing, James A Votava, Jorgo Lika, Andrew S Wagner, Simone Shen, Nicholas L Arp, Hamidullah Khan, Stefan M Schieke, Christopher D Fletcher and 2 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Article
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  4. The pyruvate branch point controls lymphoid cancer cell dissemination.bioRxiv : the preprint server for biology · 2026
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  6. Review
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  13. Review
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  15. Activation induces shift in nutrient utilization that differentially impacts cell functions in human neutrophils.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  16. Article
  17. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Emily C BrittMorgridge Institute for Research, Madison, WI 53715.
Xin QingMorgridge Institute for Research, Madison, WI 53715.
James A VotavaMorgridge Institute for Research, Madison, WI 53715.ORCID 0000-0002-1452-4468
Jorgo LikaMorgridge Institute for Research, Madison, WI 53715.ORCID 0000-0003-4563-7569
Andrew S WagnerDepartment of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, WI 53706.
Simone ShenDepartment of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, WI 53706.
Nicholas L ArpMorgridge Institute for Research, Madison, WI 53715.ORCID 0000-0001-8709-0667
Hamidullah KhanDepartment of Dermatology, University of Wisconsin-Madison, Madison, WI 53715.
Stefan M SchiekeDepartment of Dermatology, University of Wisconsin-Madison, Madison, WI 53715.
Christopher D FletcherUniversity of Wisconsin Carbone Cancer Center, Madison, WI 53792.
Anna HuttenlocherCell and Molecular Biology Graduate Program, University of Wisconsin-Madison, Madison, WI 53706.ORCID 0000-0001-7940-6254
Jing FanMorgridge Institute for Research, Madison, WI 53715.

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Christian Capitini · 1985 to 2026
$142.6M
University of Wisconsin Institute for Clinical and Translational ResearchUL1TR002373 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI ELIZABETH S BURNSIDE, Allan R. Brasier · 2017 to 2026
$75.9M
NRSA Training CoreTL1TR002375 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI Vivek Prabhakaran · 2017 to 2026
$8.4M
Cell migration and wound repairR35GM118027 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Anna Huttenlocher · 2016 to 2026
$7.5M
Integrated Training For Physician-ScientistsT32GM140935 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Anna Huttenlocher, Jeniel E Nett · 2021 to 2026
$6.5M
Metabolic rewiring coupled to the production of reactive oxygen and nitrogen species (RONS)R35GM147014 · NIGMS · MORGRIDGE INSTITUTE FOR RESEARCH, INC. · PI Jing Fan · 2022 to 2026
$2.1M
HHS | NIH | National Center for Advancing Translational Sciences (NCATS) TL1TR002375HHS | NIH | National Center for Advancing Translational Sciences (NCATS) UL1TR002373HHS | NIH | National Institute of General Medical Sciences (NIGMS) R35GM118027HHS | NIH | National Institute of General Medical Sciences (NIGMS) R35GM147014HHS | NIH | National Institute of General Medical Sciences (NIGMS) T32GM140935NCATS NIH HHS TL1 TR002375NCATS NIH HHS UL1 TR002373NCI NIH HHS P30 CA014520NIGMS NIH HHS R35 GM118027NIGMS NIH HHS R35 GM147014NIGMS NIH HHS T32 GM140935University of Wisconsin-Madison Office of the Vice Chancellor for Research and Graduate Education AAH8454
6 · The paper itself

Abstract

Neutrophils utilize a variety of metabolic sources to support their crucial functions as the first responders in innate immunity. Here, through in vivo and ex vivo isotopic tracing, we examined the contributions of different nutrients to neutrophil metabolism under specific conditions. Human peripheral blood neutrophils, in contrast to a neutrophil-like cell line, rely on glycogen storage as a major metabolic source under resting state but rapidly switch to primarily using extracellular glucose upon activation with various stimuli. This shift is driven by a substantial increase in glucose uptake, enabled by rapidly increased GLUT1 on cell membrane, that dominates the simultaneous increase in gross glycogen cycling capacity. Shifts in nutrient utilization impact neutrophil functions in a function-specific manner: oxidative burst depends on glucose utilization, whereas NETosis and phagocytosis can be flexibly supported by either glucose or glycogen, and neutrophil migration and fungal control are enhanced by the shift from glycogen utilization to glucose utilization. This work provides a quantitative and dynamic understanding of fundamental features in neutrophil metabolism and elucidates how metabolic remodeling shapes neutrophil functions, which has broad health relevance.

Indexed as

GlucoseGlycogenNeutrophilsPhagocytosisExtracellular TrapsGlucose Transporter Type 1HumansNeutrophil ActivationNutrientsRespiratory BurstGlucoseGlucose Transporter Type 1GlycogenNutrientsSLC2A1 protein, humanimmunometabolismneutrophilnutrient dependencenutrient preference switch

Identifiers

PMID39284072
PMCPMC11441510

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.