Evidence map›Paper›PMID 41890721›Full record

ArticleFrontiers in immunology2026

A semi-automated imaging and analysis pipeline for NET quantification and temporal-profiling of NETosis.

Chloé Landry, Liyuan Wang, Emma Gerber, Chet Elliot Holterman, Dylan Burger

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

5 authors.

Chloé LandryKidney Research Centre, Inflammation and Chronic Disease Program, The Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Liyuan WangCell Biology and Image Acquisition Core Facility, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.
Emma GerberKidney Research Centre, Inflammation and Chronic Disease Program, The Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Chet Elliot HoltermanKidney Research Centre, Inflammation and Chronic Disease Program, The Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Dylan BurgerKidney Research Centre, Inflammation and Chronic Disease Program, The Ottawa Hospital Research Institute, Ottawa, ON, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

NETosis is a distinct form of neutrophil cell death involved in innate immunity and characterized by the release of DNA, that when dysregulated contributes to tissue damage and target-organ injury. As our understanding of the mechanisms governing this process continues to advance, there is a growing need for refined tools that can precisely characterize NETosis and enable efficient screening of its modulators. Here, we present a novel live-cell imaging and analysis pipeline for quantifying NETosis in cultured cells. We have generated a CellProfiler pipeline that enables in-depth analysis of cell and NET features, allowing for subsequent characterization and classification of NETosis stages using machine learning. Coupled with high throughput live cell imaging, this approach allows for large-scale and automated tracking of NETosis progression. The pipeline was validated in promyelocytic HL-60 cells differentiated into granulocyte-like cells, as well as primary neutrophils from the bone marrow of mice. We further confirmed dose and stimulus-dependent responses to common stimuli and pharmacological inhibitors of NETosis. As a flexible and scalable high-throughput imaging pipeline, our novel approach allows for the assessment of NETting dynamics and the screening of potential NETosis-modulating agents, which will be instrumental in developing therapies for NET-induced tissue injury.

Indexed as

Extracellular TrapsImage Processing, Computer-AssistedNeutrophilsAnimalsHL-60 CellsHumansMachine LearningMicehigh throughput analysislive-cell imagingmachine learningNETsneutrophil extracellular trapsquantification pipeline

Identifiers

PMID41890721
PMCPMC13012954

What Socratic 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 Socratic graph.