| Literature DB >> 33704712 |
Sanni Alve1, Silvia Gramolelli1, Päivi M Ojala2,3.
Abstract
Three-dimensional (3D) cell culture has allowed a deeper understanding of complex pathological and physiological processes, overcoming some of the limitations of 2D cell culture on plastic and avoiding the costs and ethical issues related to experiments involving animals. Here we describe a protocol to embed single melanoma cells alone or together with primary human lymphatic endothelial cells in a 3D cross-linked matrix, to investigate the invasion and molecular crosstalk between these two cell types, respectively. After fixation and staining with antibodies and fluorescent conjugates, phenotypic changes in both cell types can be specifically analyzed by confocal microscopy.Entities:
Keywords: 3D cell culture; Co-culture; Fibrin matrix; Immunofluorescence; Invasion; Lymphatic endothelial cells; Melanoma; Molecular crosstalk; Sprouting
Mesh:
Year: 2021 PMID: 33704712 DOI: 10.1007/978-1-0716-1205-7_11
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745