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Immune surveillance is an integral part of the innate immune system, involving the continuous monitoring of peripheral tissues to detect and respond to pathogens, infected cells, or cancerous cells. This surveillance is conducted primarily by natural killer (NK) cells and phagocytes, which employ distinct but complementary mechanisms to identify and eliminate threats.
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Light-Responsive Surface Topographies Modulate Macrophage Immune Responses Through Dynamic Mechanical Cues.

Oksana K Savchak1,2, Ruth M C Verbroekken2,3, Burcu Gumuscu1,2,4

  • 1Biosensors and Devices Laboratory, Department of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, The Netherlands.

Macromolecular Bioscience
|February 28, 2026
PubMed
Summary
This summary is machine-generated.

Dynamic liquid crystal (LC) polymer films precisely control macrophage responses using light-induced topographies. These tunable surfaces offer new strategies for immune modulation and regenerative medicine therapies.

Keywords:
dynamic topographiesimmunomodulationlamellipodialiquid crystal polymersmacrophagemateriobiologymechanobiologyphenotype modulationphoto‐responsive materials

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Area of Science:

  • Biomaterials Science
  • Cell Biology
  • Immunology

Background:

  • Macrophage phenotype regulation by mechanical cues is crucial for understanding inflammation and developing therapies.
  • Current methods for controlling mechanical stimuli lack dynamic, real-time, and reversible capabilities.
  • Dynamic interfaces are needed to precisely manipulate cell behavior through mechanical cues.

Purpose of the Study:

  • To investigate the immunomodulatory effects of dynamic liquid crystal (LC) polymer films on macrophage responses.
  • To explore the use of reversible light-induced LC surface topographies for on-demand cell reprogramming.
  • To assess topography-dependent macrophage behavior and cytokine expression profiles.

Main Methods:

  • Utilized dynamic liquid crystal (LC) polymer films with reversible light-induced surface topographies (flat, pillared, grooved).
  • Exposed THP-1-derived macrophages to these dynamic topographies to study cell responses.
  • Analyzed macrophage pro- and anti-inflammatory markers, cytokine expression, and membrane morphology.

Main Results:

  • Grooved LC films significantly increased both pro- and anti-inflammatory markers.
  • Pillared LC films maintained an anti-inflammatory profile without broad activation.
  • Dynamic topographies induced distinct changes in macrophage membrane morphology, including blebbing and lamellipodia/filopodia formation.

Conclusions:

  • Light-responsive LC surfaces provide a controllable platform for topography-dependent immune modulation.
  • Macrophage plasticity can be exploited using these dynamic scaffolds for regenerative medicine.
  • Tunable mechanical stimuli from LC surfaces offer opportunities for adaptive immune regulation.