Evidence map›Paper›PMID 40318038›Full record

ArticleACS applied materials & interfaces2025

Light-Responsive Liquid Crystal Surface Topographies for Dynamic Stimulation of Cells.

Ruth M C Verbroekken, Oksana K Savchak, Thom F J Alofs, Albert P H J Schenning, Burcu Gumuscu

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Ruth M C VerbroekkenStimuli-Responsive Functional Materials and Devices, Department of Chemical Engineering and Chemistry, Eindhoven University of Technology, P.O. Box 513, Eindhoven 5600 MB, The Netherlands.
Oksana K SavchakInstitute for Complex Molecular Systems, Eindhoven University of Technology, P.O. Box 513, Eindhoven 5600 MB, The Netherlands.
Thom F J AlofsStimuli-Responsive Functional Materials and Devices, Department of Chemical Engineering and Chemistry, Eindhoven University of Technology, P.O. Box 513, Eindhoven 5600 MB, The Netherlands.
Albert P H J SchenningStimuli-Responsive Functional Materials and Devices, Department of Chemical Engineering and Chemistry, Eindhoven University of Technology, P.O. Box 513, Eindhoven 5600 MB, The Netherlands.ORCID 0000-0002-3485-1984
Burcu GumuscuInstitute for Complex Molecular Systems, Eindhoven University of Technology, P.O. Box 513, Eindhoven 5600 MB, The Netherlands.ORCID 0000-0003-4843-4724

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

All biological surfaces possess distinct dynamic surface topographies. Due to their versatility, these topographies play a crucial role in modulating cell behavior and, when intentionally designed, can precisely guide cellular responses. So far, biomechanical responses have predominantly been studied on static surfaces, overlooking the dynamic environment in the body, where cells constantly interact with shifting biomechanical cues. In this work, we designed and fabricated a light-responsive liquid crystal polymer film to study the effect of micrometer-scale, dynamic surface topographies on cells under physiologically relevant conditions. The light-responsive liquid crystal polymers enable on-demand surface topographical changes, reaching pillar heights of 800 nm and grooved topographies with 700 nm height differences at 37 °C in water. The light-induced surface topographies increased mechanosensitive cell signaling by up to 2-fold higher yes-associated protein (YAP) translocation to the nucleus, as well as up to 3-fold more heterogeneity in distribution of focal adhesions, in a topography-related manner. The pillared topography was seen to cause a lower cellular response, while the grooved topography caused an increased mechanical activation, as well as cell alignment due to a more continuous and aligned physical cue that enhances cell organization. Excitingly, we observed that subsequent surface topography changes induced a 3-fold higher YAP nuclear translocation in fibroblast cells, as well as a 5-fold higher vinculin heterogeneity distribution, indicating that multiple cycles of topography exposure ampliated the cell response. Our work emphasizes the potential of light-responsive liquid crystal polymer films generating dynamic biomechanical cues that allow us to modulate and steer cells in vitro.

Indexed as

FibroblastsLightLiquid CrystalsSurface PropertiesBiomechanical PhenomenaCell NucleusHumansMaterials TestingPolymersYAP-Signaling Proteinsliquid crystal polymerPolymersYAP-Signaling Proteinsfibroblast cellslight-responsive liquid crystal polymersmateriobiologymechanical cell-stimulationreconfigurable dynamic topographiessurface actuation

Identifiers

PMID40318038
PMCPMC12086769

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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 OpenQuestion graph.