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Measuring cell displacements in opaque tissues: dynamic light scattering in the multiple scattering regime
Benjamin Brunel1, Vincent Levy1, Arnaud Millet2,3
1Université Grenoble Alpes, Laboratoire Interdisciplinaire de Physique, CNRS, F-38000 Grenoble, France.
Biomedical Optics Express
|April 29, 2020
Summary
This study introduces a new method to analyze light scattering fluctuations, revealing cell movement dynamics within thick biological tissues. The findings offer insights into cellular motility in complex, three-dimensional environments.
Area of Science:
- Biophysics
- Optical Imaging
- Cell Biology
Background:
- Standard imaging techniques struggle to probe deep tissue structures and dynamics.
- Dynamic light scattering and diffusive wave spectroscopy analyze cellular dynamics in thin and thick samples, respectively.
- An intermediate scattering regime remains largely unexplored for quantitative analysis.
Purpose of the Study:
- To develop an analytical framework for light scattering in the intermediate regime.
- To establish a relationship between scattered light fluctuations and cell displacement distributions.
- To characterize cell motility within thick multicellular aggregates.
Main Methods:
- Utilized coherent light scattering to probe biological tissues.
- Developed an analytical model connecting scattered light fluctuations to cellular dynamics.
- Applied the method to analyze cell motility in millimeter-thick multicellular aggregates.
Main Results:
- Established an analytical relationship for the intermediate light scattering regime.
- Quantified cell displacement distributions over time from scattered light.
- Successfully characterized cell motility within 0.5 mm thick multicellular aggregates.
Conclusions:
- The developed method bridges the gap between single and multiple scattering regimes for light.
- Provides a novel approach to study deep tissue cellular dynamics non-invasively.
- Offers a powerful tool for investigating cell motility in complex biological systems.

