Evidence map›Paper›PMID 41280342›Full record

ArticlePNAS nexus2025

A novel method for evaluating and visualizing scratch wound healing assays using level-set and image sector analysis.

Markéta Vašinková, Michal Krumnikl, Arootin Gharibian, Ondřej Mičulek, Eva Kriegová, Petr Gajdoš

Abstract read
In one paragraph

Article in PNAS nexus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Nanosponge-integrated hydrogel ofFrontiers in pharmacology · 2026
    Article
  3. 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

6 authors.

Markéta VašinkováDepartment of Computer Science, FEECS, VSB - Technical University of Ostrava, 17. listopadu 2172/15, Ostrava 70800, Czech Republic.ORCID https://orcid.org/0009-0003-9321-0751
Michal KrumniklDepartment of Computer Science, FEECS, VSB - Technical University of Ostrava, 17. listopadu 2172/15, Ostrava 70800, Czech Republic.ORCID https://orcid.org/0000-0002-6153-4212
Arootin GharibianDepartment of Computer Science, FEECS, VSB - Technical University of Ostrava, 17. listopadu 2172/15, Ostrava 70800, Czech Republic.ORCID https://orcid.org/0000-0001-7819-0842
Ondřej MičulekDepartment of Computer Science, FEECS, VSB - Technical University of Ostrava, 17. listopadu 2172/15, Ostrava 70800, Czech Republic.
Eva KriegováFaculty of Medicine and Dentistry, Palacky University & University Hospital, Hněvotínská 3, Olomouc 77900, Czech Republic.ORCID https://orcid.org/0000-0002-8969-4197
Petr GajdošDepartment of Computer Science, FEECS, VSB - Technical University of Ostrava, 17. listopadu 2172/15, Ostrava 70800, Czech Republic.ORCID https://orcid.org/0000-0003-1831-3489

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Scratch wound healing assays are widely used to study collective cell migration, essential for understanding tissue regeneration, drug effects, and wound healing mechanisms. However, conventional analyses often rely on wound edge dynamics or individual cell tracks, limiting spatial insight into migration behavior. We present a sector-based analytical framework that reinterprets time-lapse microscopy data by dividing each image into defined spatial regions across the field of view. This enables spatially resolved characterization of how cell populations migrate over time. To address challenges of low contrast and uneven illumination in bright-field microscopy, we apply a level-set segmentation algorithm that robustly detects the wound edge. Using this approach, we show that both cell velocity and trajectory vary with distance from the wound boundary. We introduce a novel metric, the sector-boundary distance, to identify regions where cells migrate faster along nonradial paths. To assess chemotactic activation, cells were treated with the chemokine CXCL10 to stimulate motility via CXCR3-mediated signaling. Statistical testing showed that, in treated cells, the proportion of highly motile cells was significantly associated with wound closure, even in regions distant from the scratch, whereas directionality played a limited role. By contrast, untreated cells exhibited weaker and less organized migration patterns. These findings highlight how local cellular activity contributes to healing in a treatment-dependent manner. Our method bridges global wound-level analysis and local cell-scale behavior by combining single-cell tracking with precise boundary detection. The complete framework is available as open-source software, including a user-friendly web application that enables interactive analysis of microscopy data.

Indexed as

collective cell migrationimage processinglevel-setsscratch wound healing assaytime-lapse microscopy

Identifiers

PMID41280342
PMCPMC12637207

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.