In this video, we demonstrate the development of an in vitro three-dimensional model of the lining of the peritoneal cavity. This organotypic culture can help to investigate ovarian cancer cell adhesion, invasion, and proliferation.
Protocol
1. Plating the Organotypic Culture Release NOF (normal omental fibroblasts ) from a 75 cm2 culture flask by rinsing with 10 ml of PBS followed by 3 ml of 0.25% trypsin/25 mM EDTA for no more than 5 min. Neutralize trypsin with at least 3 times the volume of full growth media. Transfer trypsinized cells into a 50 ml conical tube and spin down at 0.5 g x 3 min. Remove supernatant and bring cells back up in 5 ml of full growth media. Use a cell counter to count the cell…
Açıklamalar
The authors have nothing to disclose.
Materials
PBS
Fisher Scientific
SH3001304
15 cm culture dishes
BD Biosciences
353025
DMEM with L-Glutamine
Corning
10-013-CV
MEM Vitamins
Corning
25-020-Cl
MEM Nonessential amino acids
Corning
25-025-CI
Penicillin-Streptomycin
Corning
30-002-CI
Shaker
Thermo-Fisher
MaxQ 4450
Centrifuge
Eppendorf
5702
Incubator
Thermo-Fisher
Forma Series II Water Jacketed
CO2 Incubator Model 3100
Modeling Ovarian Cancer Metastasis in Peritoneal Cavity Lining: A Method To Establish an In Vitro 3D Model of the Peritoneal Lining. J. Vis. Exp. (Pending Publication), e20375, doi: (2023).