Evidence map›Paper›PMID 40667183›Full record

ArticlebioRxiv : the preprint server for biology2025

Methodological study of fibroblasts MEF 3T3 heterogeneity cultured on hydrogel substrates with different surface functionalization.

Dawid Wawrzyk, Paweł Goncerz, Zenon Rajfur

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Dawid WawrzykInstitute of Physics, Faculty of Physics, Astronomy and Applied Computer Science, Jagiellonian University, 30-348 Kraków, Poland.
Paweł GoncerzInstitute of Physics, Faculty of Physics, Astronomy and Applied Computer Science, Jagiellonian University, 30-348 Kraków, Poland.
Zenon RajfurInstitute of Physics, Faculty of Physics, Astronomy and Applied Computer Science, Jagiellonian University, 30-348 Kraków, Poland.ORCID 0000-0003-1265-6480

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, cellular heterogeneity has gained attention in several scientific studies. It's a phenomenon of the occurrence of differences in cellular parameters, for example, morphology or migration parameters of cells from a single cell line. It has been studied primarily in cancer cells; however, normal cells exhibit analogous behavior. This study investigated morphological and migratory parameters heterogeneity in mouse embryonic fibroblast (MEF 3T3) cells cultured on polyacrylamide (PA) substrates with elasticity of 20 and 40 kPa, which were functionalized with fibronectin solutions in 1, 5, 10 and 20 μg/ml concentrations. Two-hour time lapse microscopy made it possible to quantify the cells spread area and velocity. Based on these parameters and observations of cellular migration strategies, it was possible to classify normal cells into four subpopulations - mesenchymal, amoeboid, slow amoeboid and polygonal/bigonal. Cells grown on softer substrates (20 kPa) showed a greater sensitivity to fibronectin than those grown on stiffer substrates. Cells area was maximal, with the lowest velocity for cells grown on PA substrates functionalized with a 10 μg/ml solution, making their parameters closest to those grown on glass. Cells underwent spontaneous transitions between subpopulations, but no direct transition between mesenchymal and amoeboid or slow amoeboid has been observed. Overall, substrate elasticity and concentration of fibronectin in the functionalizing solution impact the morphology and migration parameters of cells. These findings demonstrate the occurrence of heterogeneity phenomenon in normal mouse fibroblasts. This study also shows the impact of the concentration of fibronectin in the functionalization solution on cells' behavior.

Identifiers

PMID40667183
PMCPMC12262422

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