Effects of substrate patterning on cellular spheroid growth and dynamics measured by gradient light interference microscopy (GLIM). Issue 12 (3rd October 2019)

• Record Type: Journal Article
• Authors: Fanous, Michael J.; Li, Yanfen; Kandel, Mikhail E.; Abdeen, Amr A.; Kilian, Kristopher A.; Popescu, Gabriel
• Is Part Of: Journal of biophotonics. Volume 12:Issue 12(2019)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2019-10-03
• Subjects: 3D cellular dynamics -- dispersion analysis -- label free imaging -- organoids -- quantitative phase imaging -- radial transport -- substrate engineering; Photonics -- Periodicals; Optical materials -- Periodicals; Optics -- Periodicals; Medical instruments and apparatus -- Periodicals; 621.3605
• DOI: 10.1002/jbio.201900178
• Languages: English
• ISSNs: 1864-063X

Abstract

Abstract: The development of three‐dimensional (3D) cellular architectures during development and pathological processes involves intricate migratory patterns that are modulated by genetics and the surrounding microenvironment. The substrate composition of cell cultures has been demonstrated to influence growth, proliferation and migration in 2D. Here, we study the growth and dynamics of mouse embryonic fibroblast cultures patterned in a tissue sheet which then exhibits 3D growth. Using gradient light interference microscopy (GLIM), a label‐free quantitative phase imaging approach, we explored the influence of geometry on cell growth patterns and rotational dynamics. We apply, for the first time to our knowledge, dispersion‐relation phase spectroscopy (DPS) in polar coordinates to generate the radial and rotational cell mass‐transport. Our data show that cells cultured on engineered substrates undergo rotational transport in a radially independent manner and exhibit faster vertical growth than the control, unpatterned cells. The use of GLIM and polar DPS provides a novel quantitative approach to studying the effects of spatially patterned substrates on cell motility and growth. Abstract : Gradient light interference microscopy (GLIM), a label‐free phase imaging technique, is used to analyze the growth and dynamics of mouse embryonic fibroblasts cultured on circular substrates. The patterned cells exhibit unique three‐dimensional development. Dispersion‐relation phase spectroscopy (DPS) is applied in polar coordinates to study the radial and rotational cell mass‐transport. GLIM and polar DPS comprise a novel quantitative method to assess the influence of substrates on cell motility and growth.