Evidence map›Paper›PMID 35200139›Full record

ArticleeLife2022

In vivo fluorescence lifetime imaging of macrophage intracellular metabolism during wound responses in zebrafish.

Veronika Miskolci, Kelsey E Tweed, Michael R Lasarev, Emily C Britt, Alex J Walsh, Landon J Zimmerman, Courtney E McDougal, Mark R Cronan, Jing Fan, John-Demian Sauer and 2 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 5% 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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
  2. Deletion ofBiology · 2026
    Article
  3. Review
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  7. Article
  8. Mechanisms and therapeutic insights from zebrafish models of wound healing.Frontiers in cell and developmental biology · 2026
    Review
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  10. Article
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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

12 authors at 3 institutions in 1 country.

Veronika MiskolciDepartment of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, United States.ORCID 0000-0001-7900-4626
Kelsey E TweedMorgridge Institute for Research, Madison, United States.
Michael R LasarevDepartment of Biostatistics & Medical Informatics, University of Wisconsin-Madison, Madison, United States.ORCID 0000-0002-1896-2705
Emily C BrittMorgridge Institute for Research, Madison, United States.
Alex J WalshMorgridge Institute for Research, Madison, United States.ORCID 0000-0003-3832-8207
Landon J ZimmermanDepartment of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, United States.
Courtney E McDougalDepartment of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, United States.
Mark R CronanDepartment of Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, United States.
Jing FanMorgridge Institute for Research, Madison, United States.
John-Demian SauerDepartment of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, United States.ORCID 0000-0001-9367-794X
Melissa C SkalaMorgridge Institute for Research, Madison, United States.
Anna HuttenlocherDepartment of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, United States.ORCID 0000-0001-7940-6254
University of Wisconsin–Madison · USDuke University · USMorgridge Institute for Research · US

Funding

Cell migration and wound repairR35GM118027 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Anna Huttenlocher · 2016 to 2026
$7.5M
Biotechnology Training ProgramT32GM135066 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI SCOTT M. COYLE, BRIAN G FOX · 2020 to 2026
$7.0M
Microbial Pathogenesis &Host Responses Training ProgramT32AI055397 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI KLEIN, BRUCE STEVEN · 2003 to 2024
$5.5M
Identification and Characterization of Genes Required for Listeria monocytogenes Cytosolic SurvivalR01AI137070 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI SAUER, JOHN-DEMIAN · 2018 to 2022
$2.9M
(PQ7) Quantitative in vivo optical imaging of tumor heterogeneityR01CA205101 · NCI · MORGRIDGE INSTITUTE FOR RESEARCH, INC. · PI SKALA, MELISSA CAROLINE · 2016 to 2020
$1.9M
Modulating the Inflammasome to Generate Robust Cell Mediated ImmunityR01CA188034 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI SAUER, JOHN-DEMIAN · 2015 to 2019
$1.7M
Imaging Immunometabolism in live animals during host defenseR21AI159312 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI HUTTENLOCHER, ANNA · 2021 to 2022
$423k
Metabolic regulation of macrophage-dependent wound healing in vivoK99GM138699 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI MISKOLCI, VERONIKA · 2021 to 2022
$200k
NCI NIH HHS R01 CA188034NCI NIH HHS R01 CA205101NIAID NIH HHS R01 AI137070NIAID NIH HHS R21 AI159312NIAID NIH HHS T32 AI055397NIGMS NIH HHS K99 GM138699NIGMS NIH HHS R35 GM118027NIGMS NIH HHS T32 GM135066
6 · The paper itself

Abstract

The function of macrophages in vitro is linked to their metabolic rewiring. However, macrophage metabolism remains poorly characterized in situ. Here, we used two-photon intensity and lifetime imaging of autofluorescent metabolic coenzymes, nicotinamide adenine dinucleotide (phosphate) (NAD(P)H) and flavin adenine dinucleotide (FAD), to assess the metabolism of macrophages in the wound microenvironment. Inhibiting glycolysis reduced NAD(P)H mean lifetime and made the intracellular redox state of macrophages more oxidized, as indicated by reduced optical redox ratio. We found that TNFα+ macrophages had lower NAD(P)H mean lifetime and were more oxidized compared to TNFα- macrophages. Both infection and thermal injury induced a macrophage population with a more oxidized redox state in wounded tissues. Kinetic analysis detected temporal changes in the optical redox ratio during tissue repair, revealing a shift toward a more reduced redox state over time. Metformin reduced TNFα+ wound macrophages, made intracellular redox state more reduced and improved tissue repair. By contrast, depletion of STAT6 increased TNFα+ wound macrophages, made redox state more oxidized and impaired regeneration. Our findings suggest that autofluorescence of NAD(P)H and FAD is sensitive to dynamic changes in intracellular metabolism in tissues and can be used to probe the temporal and spatial regulation of macrophage metabolism during tissue damage and repair.

Indexed as

AnimalsFemaleFlavin-Adenine DinucleotideFluorescenceGlycolysisKineticsMacrophagesMiceMice, Inbred C57BLMicroscopy, Fluorescence, MultiphotonNADPOxidation-ReductionTumor Necrosis Factor-alphaWounds and InjuriesZebrafishFlavin-Adenine DinucleotideNADPTumor Necrosis Factor-alphacell biologyFLIMimmunologyimmunometabolisminflammationmacrophagesmouseNAD(P)Hoptical redox ratiowound healingzebrafish

Identifiers

PMID35200139
PMCPMC8871371
OpenAlexW4213074404

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.