Issue 40, 2024

Visualizing and quantifying dynamic cellular forces with photonic crystal hydrogels

Abstract

Cellular forces play a crucial role in numerous biological processes, including tissue development, morphogenesis, and disease progression. However, existing methods for detecting cellular forces, such as traction force microscopy and atomic force microscopy, often face limitations in terms of high throughput, real-time monitoring, and applicability to complex biological systems. In this study, we utilized a novel Photonic Crystal Cellular Force Microscopy (PCCFM) system to visualize and quantify dynamic cellular forces. This system consists of a conventional optical microscope and a photonic crystal substrate formed by the periodic arrangement of silica nanoparticles within polyacrylamide hydrogels. Taking MDCK cells and BMSCs as examples, we found that PCCFM can capture dynamic cellular forces with high spatial and temporal resolution during the cell adhesion, spread, proliferation, and osteogenic differentiation. The application of this technique revealed distinct force patterns in different cellular stages, offering insights into the interplay between cellular forces and morphological changes. By investigating the migration of cells from MDCK cyst fragments, we could gain significant insights into tumour cell migration behaviours. The real-time, high-throughput analysis of cellular biomechanics from the PCCFM system offers valuable information on the mechanisms of tumour metastasis, potentially guiding therapeutic development and improving disease treatment strategies.

Graphical abstract: Visualizing and quantifying dynamic cellular forces with photonic crystal hydrogels

Supplementary files

Article information

Article type
Paper
Submitted
09 Jul 2024
Accepted
15 Sep 2024
First published
16 Sep 2024

Nanoscale, 2024,16, 19074-19085

Visualizing and quantifying dynamic cellular forces with photonic crystal hydrogels

J. Zhou, Y. Zhang, Y. Fu, Q. Li, J. Zhang, X. Liu and Z. Gu, Nanoscale, 2024, 16, 19074 DOI: 10.1039/D4NR02834A

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