| Literature DB >> 33742394 |
Faramarz Dehghani1, Carsten Hagemann2, Ellina Schulz3, Tim Hohmann1, Urszula Hohmann1, Ralf-Ingo Ernestus3, Mario Löhr3.
Abstract
Brain metastasis is a major challenge for therapy and defines the end stage of tumor progression with a very limited patients' prognosis. Experimental setups that faithfully mimic these processes are necessary to understand the mechanism of brain metastasis and to develop new improved therapeutic strategies. Here, we describe an in vitro model, which closely resembles the in vivo situation. Organotypic hippocampal brain slice cultures (OHSCs) prepared from 3- to 8-day-old mice are well suited for neuro-oncology research including brain metastasis. The original morphology is preserved in OHSCs even after culture periods of several days to weeks. Tumor cells or cells of metastatic origin can be seeded onto OHSCs to evaluate micro-tumor formation, tumor cell invasion, or treatment response. We describe preparation and culture of OHSCs including the seeding of tumor cells. Finally, we show examples of how to treat the OHSCs for life-dead or immunohistochemical staining.Entities:
Keywords: Brain tumor; Cryosection; Glioblastoma; Glioma; Immunohistochemistry; Invasion; Life–dead staining; Metastasis; Organotypic hippocampal slice cultures (OHSCs)
Mesh:
Year: 2021 PMID: 33742394 DOI: 10.1007/978-1-0716-1350-4_5
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745