Abstract
Intestinal organoid cultures are a powerful tool to study epithelial cells in vitro, as they are able to proliferate and differentiate into all cell lineages observed in vivo. Co-culturing organoids with distinct genetic backgrounds provides an excellent approach to study contact dependent and independent interactions between healthy and mutant epithelial intestinal cells. Here, we provide 2D and 3D approaches to mouse organoid co-cultures using fluorescently labeled organoids and demonstrate the analysis of these co-cultures using flow cytometry and microscopy-based approaches. For complete details on the use and execution of this profile, please refer to van Neerven et al., 2021.
| Original language | English |
|---|---|
| Article number | 101050 |
| Journal | STAR Protocols |
| Volume | 3 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 18 Mar 2022 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Cancer
- Cell Biology
- Cell culture
- Cell-based Assays
- Flow Cytometry/Mass Cytometry
- Microscopy
- Organoids
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