Isolation and Characterization of Extracellular Vesicles from Cell Culture Conditioned Medium for Immunological Studies

Abstract

Extracellular vesicles (EVs) are small, membranous particles that have recently emerged as one the most important mediators of intercellular communication. They can contain a variety of proteins, lipids, and nucleic acids and thus are responsible for modulation of multiple biological processes, including immune response and regulation of immune cells. Immunomodulatory activity of different EVs can be reliably assessed using EVs isolated from cell culture conditioned medium and added to in vitro or ex vivo cultures of immune cells. This article describes protocols for isolation of EVs from cell culture supernatants by differential ultracentrifugation and density gradient centrifugation. It also provides tools and protocols that enable characterization and validation of isolated particles, as well as analysis of interactions between EVs of interest and different subpopulations of human immune cells. © 2020 Wiley Periodicals LLC.

Basic Protocol 1: Isolation of extracellular vesicles by differential ultracentrifugation

Basic Protocol 2: Isolation of extracellular vesicles by density gradient centrifugation

Support Protocol 1: Imaging of extracellular vesicles using transmission electron microscopy

Support Protocol 2: Detection of extracellular vesicle protein markers by Western blotting

Support Protocol 3: Measurement and counting of extracellular vesicles by nanoparticle tracking analysis

Basic Protocol 3: Analysis of extracellular vesicle uptake or association by different subpopulations of lymphocytes in vitro