Organotypic 3D Ex Vivo Co-culture Model of the Macro-metastasis/Organ Parenchyma Interface.
Raquel BlazquezDaniela SparrerJessica SonbolJürgen PhilippFlorian SchmiederTobias PukropPublished in: Methods in molecular biology (Clifton, N.J.) (2024)
The macro-metastasis/organ parenchyma interface (MMPI) is gaining increasing significance due to its prognostic relevance for cancer (brain) metastasis. We have developed an organotypic 3D ex vivo co-culture model that mimics the MMPI and allows us to evaluate the histopathological growth pattern (HGP) and infiltration grade of the tumor cells into the neighboring brain tissue and to study the interactions of cancer and glial cells ex vivo. This system consists of a murine brain slice and a 3D tumor plug that can be co-cultured for several days. After slicing the brain of 5- to 8-day-old mice, a Matrigel plug containing fluorescent-labelled tumor cells is placed next to it, so that tumor cells in the 3D plug and glial cells in the brain slice can interact at the interface for up to 96 h. To facilitate the positioning of the co-culture and increase the reproducibility of the model, a brain spacer can be used. The HGP and infiltration of the tumor cells into the brain slice as well as the activation of the glial cells can be assessed by live and/or confocal microscopy after immunofluorescence staining of microglia and/or astrocytes. Alternatively, the co-culture can also be used for other purposes, such as RNA analysis. This organotypic 3D ex vivo co-culture offers a perfect tool for preliminary screenings before in vivo experiments and reduces the number of animals, thus contributing to the 3R concept as a central precept in preclinical research.
Keyphrases
- resting state
- white matter
- induced apoptosis
- cerebral ischemia
- cell cycle arrest
- neuropathic pain
- magnetic resonance imaging
- metabolic syndrome
- computed tomography
- stem cells
- papillary thyroid
- type diabetes
- adipose tissue
- endoplasmic reticulum stress
- endothelial cells
- signaling pathway
- skeletal muscle
- insulin resistance
- living cells
- data analysis