| Literature DB >> 33565979 |
Sara Elgamal1, Federico Colombo2, Francesca Cottini3, John C Byrd4, Emanuele Cocucci5.
Abstract
Recent advances in live cell imaging allow investigating processes that take place over the entire cell volume with unprecedented time and spatial resolution. Here we describe a protocol to study intercellular communication, including extracellular vesicle exchange, between cancer cells and their microenvironment, using lattice light sheet fluorescence microscopy. While the described protocol is intended to study the interactions between chronic lymphocytic leukemia cells and bone marrow stromal cells, many components of it can be applied to study other cancers of hematopoietic or solid tumor origin, as well as to characterize other modalities of intercellular communication.Entities:
Keywords: Bioreactor flask; Chronic lymphocytic leukemia; Co-culture; Exosomes; Extracellular vesicles; Fluorescence microscopy; Imaging; LLSM; Lattice light sheet microscope; Live cell microscopy
Mesh:
Year: 2020 PMID: 33565979 DOI: 10.1016/bs.mie.2020.06.015
Source DB: PubMed Journal: Methods Enzymol ISSN: 0076-6879 Impact factor: 1.600