Tumor microenvironment (TME) is a complex aggregation of malignant cells and non-transformed cells (fibroblasts, neuroendocrine cells, blood and inflammatory cells). The cells within TME have dynamic and tumor regulating functions at all stages of cancer (initiation, progression and metastasis).
Three-dimensional (3D) cell culture systems provide physiologically relevant information in research and drug development more than the traditional 2D culture systems. The additional dimensionality of 3D cultures accurately mimic microenvironments and demonstrate similar cellular responses to in-vivo conditions. TrueGel3D™ hydrogel systems are biochemically defined and easy to use model systems to design biomimetic hydrogels that can mimic natural extracellular matrices (ECM). The objective of this study is to investigate the compatibility of TrueGel3D™ hydrogels for the co-culture of cancer cells and stromal cells.
All steps were performed in a sterile hood and the volume ratio of each component was added as indicated below.
When cultured alone in TrueGel3D™ hydrogels, MCF-7 breast cancer cell lines formed tumor-like spheroids whereas, the human dermal fibroblasts appeared outstretched like in physiological conditions. Co-culture of both cell types in TrueGel3D™ hydrogel retained the physiological and morphological characteristics even after 14 days, and represented a perfect tumor-stroma model to study tumor microenvironment.
Figure 1. Mono- and co-culture of MCF-7 cells and fibroblasts in TrueGel3D™ hydrogels. A: MCF-7 cells cultured alone, B: human fibroblasts cultured alone, C: Co-culture of MCF-7 and fibroblasts. Red: Actin cytoskeleton; green: nuclei. Scale bar: 100 µM.
TrueGel3D™ hydrogel support co-culture models to evaluate the effects of cell-cell interaction and secreted factors on cellular response. MCF7 cell lines grown in TrueGel3D™ hydrogels exhibit characteristics of avascular tumors and allows monitoring of spheroid formation under optical microscopy. Unlike MCF-7 monolayer cells, the spheroids are better models to study drug penetration behavior, cell apoptosis, cell cycle distribution and gene expression1.
The outstretched fibroblasts grown in a 3D environment resemble in-vivo conditions, increase cell migration and proliferative activity of cancer cells, serving better models for epithelial-mesenchymal transition2. The TrueGel3D™ hydrogel also enables post culture analysis (PCR, blotting) to investigate the effects molecular factors on cell behavior.
3D co-culture is not limited to the study of cancer biology3, but instead empirical evidence shows use in various applications including osteogenic differentiation4, chondrocyte differentiation5, angiogenesis6, drug screening7, and peripheral nerve studies8.
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