3D Microwell Platforms for Control of Single Cell 3D Geometry and Intracellular Organization

• Published in: Cellular and molecular bioengineering 2021-02, Vol.14 (1), p.1-14
• Main Authors: Wilson, Robin E., Denisin, Aleksandra K., Dunn, Alexander R., Pruitt, Beth L.
• Format: Article
• Language: English
• Subjects: Actin; Adhesion tests; Adhesives; Aspect ratio; Biological and Medical Physics; Biomaterials; Biomedical Engineering and Bioengineering; Biomedical Engineering/Biotechnology; Biophysics; Cell adhesion; Cell Biology; Cell migration; Cytology; Engineering; Gels; Geometry; Mechanical properties; Microenvironments; Modulus of elasticity; Myoblasts; Nuclear structure; Original; Original Article; Platforms; Polyacrylamide; Polymers; Swelling
• ISSN: 1865-5025; 1865-5033
• DOI: 10.1007/s12195-020-00646-9

Introduction Cell structure and migration is impacted by the mechanical properties and geometry of the cell adhesive environment. Most studies to date investigating the effects of 3D environments on cells have not controlled geometry at the single-cell level, making it difficult to understand the influence of 3D environmental cues on single cells. Here, we developed microwell platforms to investigate the effects of 2D vs. 3D geometries on single-cell F-actin and nuclear organization. Methods We used microfabrication techniques to fabricate three polyacrylamide platforms: 3D microwells with a 3D adhesive environment ( 3D / 3D ), 3D microwells with 2D adhesive areas at the bottom only ( 3D / 2D ), and flat 2D gels with 2D patterned adhesive areas ( 2D / 2D ). We measured geometric swelling and Young’s modulus of the platforms. We then cultured C2C12 myoblasts on each platform and evaluated the effects of the engineered microenvironments on F-actin structure and nuclear shape. Results We tuned the mechanical characteristics of the microfabricated platforms by manipulating the gel formulation. Crosslinker ratio strongly influenced geometric swelling whereas total polymer content primarily affected Young’s modulus. When comparing cells in these platforms, we found significant effects on F-actin and nuclear structures. Our analysis showed that a 3D/3D environment was necessary to increase actin and nuclear height. A 3D/2D environment was sufficient to increase actin alignment and nuclear aspect ratio compared to a 2D/2D environment. Conclusions Using our novel polyacrylamide platforms, we were able to decouple the effects of 3D confinement and adhesive environment, finding that both influenced actin and nuclear structure.