Document Type
Article
Publication Date
6-2024
Keywords
Multicellular spheroids; Macrophage; Metabolism; Autofluorescence; Fluorescence microscopy
Abstract
Purpose
In vitro assays are essential for studying cellular biology, but traditional monolayer cultures fail to replicate the complex three-dimensional (3D) interactions of cells in living organisms. 3D culture systems offer a more accurate reflection of the cellular microenvironment. However, 3D cultures require robust and unique methods of characterization.
Methods
The goal of this study was to create a 3D spheroid model using cancer cells and macrophages, and to demonstrate a custom image analysis program to assess structural and metabolic changes across spheroid microregions.
Results
Structural characterization shows that cells at the necrotic core show high normalized fluorescence intensities of CD206 (M2 macrophages), cellular apoptosis (cleaved caspase-3, CC3), and hypoxia (HIF-1α and HIF-2α) compared to the proliferative edge, which shows high normalized fluorescence intensities of CD80 (M1 macrophages) and cellular proliferation (Ki67). Metabolic characterization was performed using multiphoton microscopy and fluorescence lifetime imaging (FLIM). Results show that the mean NADH lifetime at the necrotic core (1.011 ± 0.086 ns) was lower than that at the proliferative edge (1.105 ± 0.077 ns). The opposite trend is shown in the A1/A2 ratio (necrotic core: 4.864 ± 0.753; proliferative edge: 4.250 ± 0.432).
Conclusion
Overall, the results of this study show that 3D multicellular spheroid models can provide a reliable solution for studying tumor biology, allowing for the evaluation of discrete changes across all spheroid microregions.
Citation
Bess, S. N., Smart, G. K., Igoe, M. J., & Muldoon, T. J. (2024). Scaffold-Free Development of Multicellular Tumor Spheroids with Spatial Characterization of Structure and Metabolic Radial Profiles. In Vitro Models, 3 (2-3), 91-108. https://doi.org/10.1007/s44164-024-00074-3
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.
Included in
Biomaterials Commons, Materials Science and Engineering Commons, Molecular, Cellular, and Tissue Engineering Commons
Comments
The version of record of this article, first published in In Vitro Models, is available online at Publisher’s website: http://dx.doi.org/10.1007/s44164-024-00074-3