Evidence map›Paper›PMID 40852713›Full record

ArticleFrontiers in immunology2025

Single cell autofluorescence imaging reveals immediate metabolic shifts of neutrophils with activation across biological systems.

Rupsa Datta, Veronika Miskolci, Gina M Gallego-López, Emily Britt, Amani Gillette, Aleksandr Kralovec, Morgan A Giese, Tongcheng Qian, James Votava, Wenxuan Zhao and 3 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Rupsa DattaMorgridge Institute for Research, Madison, WI, United States.
Veronika MiskolciDepartment of Medical Microbiology and Immunology, University of Wisconsin, Madison, WI, United States.
Gina M Gallego-LópezMorgridge Institute for Research, Madison, WI, United States.
Emily BrittMorgridge Institute for Research, Madison, WI, United States.
Amani GilletteMorgridge Institute for Research, Madison, WI, United States.
Aleksandr KralovecMorgridge Institute for Research, Madison, WI, United States.
Morgan A GieseDepartment of Medical Microbiology and Immunology, University of Wisconsin, Madison, WI, United States.
Tongcheng QianMorgridge Institute for Research, Madison, WI, United States.
James VotavaMorgridge Institute for Research, Madison, WI, United States.
Wenxuan ZhaoMorgridge Institute for Research, Madison, WI, United States.
Jing FanMorgridge Institute for Research, Madison, WI, United States.
Anna HuttenlocherDepartment of Medical Microbiology and Immunology, University of Wisconsin, Madison, WI, United States.
Melissa C SkalaMorgridge Institute for Research, Madison, WI, United States.

Funding

The Center for Label-free Imagingand Multiscale Biophotonics (CLIMB)P41EB031772 · NIBIB · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI Stephen A Boppart · 2022 to 2026
$7.6M
Cell migration and wound repairR35GM118027 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Anna Huttenlocher · 2016 to 2026
$7.5M
Functional optical imaging for rapid, label-free predictions of treatment response and clonal evolution in patient-derived cancer organoidsR01CA272855 · NCI · MORGRIDGE INSTITUTE FOR RESEARCH, INC. · PI Dustin A Deming, Melissa Caroline Skala · 2023 to 2026
$3.1M
Label-free imaging of CAR T cell metabolismR01CA278051 · NCI · MORGRIDGE INSTITUTE FOR RESEARCH, INC. · PI Christian Capitini, Krishanu Saha · 2023 to 2026
$2.6M
A multiplexed micro scale assay for real time analysis of pediatric immune cell functionU24AI152177 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI BEEBE, DAVID J, KERR, SHEENA CATHERINE · 2020 to 2024
$1.8M
Metabolic regulation of macrophage-dependent wound healing in vivoR00GM138699 · NIGMS · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI MISKOLCI, VERONIKA · 2023 to 2025
$739k
NCI NIH HHS R01 CA272855NCI NIH HHS R01 CA278051NIAID NIH HHS U24 AI152177NIBIB NIH HHS P41 EB031772NIGMS NIH HHS R00 GM138699NIGMS NIH HHS R35 GM118027
6 · The paper itself

Abstract

Introduction: Neutrophils are critical innate immune cells that heterogeneously respond to infection and inflammation by performing functions such as oxidative burst and NETosis, which require significant metabolic adaptation. Deeper insights into the single cell diversity of such metabolic changes will help identify regulation of neutrophil functions in health and diseases. Due to their short lifespan and associated technical challenges, the early metabolic processes of neutrophil activation are not completely understood. New tools are needed to measure rapid changes in neutrophil metabolism on a single cell level. Methods: To address this, we use optical metabolic imaging (OMI), which entails optical redox ratio and fluorescence lifetime imaging microscopy of intrinsic metabolic coenzymes NAD(P)H and FAD to assess the metabolic state of single neutrophils. Primary human neutrophils were imaged Results: Our findings show rapid metabolic remodeling to a reduced redox state during activation. Additionally, heterogeneous metabolic response to pathogens ( Conclusion: This work addresses the critical need for advanced single-cell tools to monitor rapid and diverse metabolic changes in neutrophils, an underexplored area with significant implications for understanding immune responses and developing therapies for inflammatory diseases. Neutrophils, the body's first responders to infection and inflammation, undergo rapid metabolic changes upon activation. Using label-free optical metabolic imaging of intrinsic metabolic coenzymes NAD(P)H and FAD, we reveal distinct metabolic signatures in activated primary human neutrophils as well as neutrophils in live zebrafish larvae. Our findings highlight how pathogens and pharmacological stimuli heterogeneously rewire neutrophil metabolism within minutes, influencing immune responses. This noninvasive method offers insights into single-cell neutrophil metabolism immediately following activation, with implications for infection, inflammation, and immune disorders.

Indexed as

Neutrophil ActivationNeutrophilsOptical ImagingSingle-Cell AnalysisAnimalsCells, CulturedFlavin-Adenine DinucleotideHumansNADPOxidation-ReductionPseudomonas aeruginosaZebrafishFlavin-Adenine DinucleotideNADPfluorescence lifetime imaging microscopy (FLIM)label-freemetabolismneutrophiloptical metabolic imagingsingle-cell

Identifiers

PMID40852713
PMCPMC12367685

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.