| Literature DB >> 35978571 |
Indra Van Zundert1, Nina Maenhoudt2, Silke De Vriendt2, Hugo Vankelecom2, Beatrice Fortuni1, Susana Rocha1.
Abstract
Over the past years, research has made impressive breakthroughs towards the development and implementation of 3D cell models for a wide range of applications, such as drug development and testing, organogenesis, cancer biology, and personalized medicine. Opposed to 2D cell monolayer culture systems, advanced 3D cell models better represent the in vivo physiology. However, for these models to deliver scientific insights, appropriate investigation techniques are required. Despite the potential of fluorescence microscopy to visualize these models with high spatial resolution, sample preparation and imaging assays are not straightforward. Here, we provide different protocols of sample preparation for fluorescence imaging, for both matrix-embedded and matrix-free models ( e.g ., organoids and spheroids, respectively). Additionally, we provide detailed guidelines for imaging 3D cell models via confocal multi-photon fluorescence microscopy. We show that using these protocols, images of 3D cell culture systems can be obtained with sub-cellular resolution. Graphical abstract.Entities:
Keywords: 3D cell culture systems ; Fluorescence Microscopy ; Multi-Photon Fluorescence Microscopy ; Organoids ; Spheroids
Year: 2022 PMID: 35978571 PMCID: PMC9350921 DOI: 10.21769/BioProtoc.4469
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325