Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

RNA interference (RNAi) has tremendous potential for specific silencing of disease-causing genes. Its clinical usage however critically depends on the development of carrier systems that can transport the RNAi-mediating small interfering RNA (siRNA) molecules to the cytosol of target cells. Recent reports have suggested that extracellular vesicles (EVs) form a natural transport system through which biomolecules, including RNA, is exchanged between cells. Therefore, EVs are increasingly being considered as potential therapeutic siRNA delivery systems.In this chapter we describe a method for preparing siRNA-loaded EVs, including a robust, scalable method to isolate them from cell culture supernatants.

Original publication

DOI

10.1007/978-1-4939-6728-5_14

Type

Journal article

Journal

Methods in molecular biology (Clifton, N.J.)

Publication Date

01/2017

Volume

1545

Pages

197 - 204

Addresses

Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK. pvader@umcutrecht.nl.

Keywords

Cell Line, Humans, RNA, Small Interfering, Cell Fractionation, Polymerase Chain Reaction, Extracellular Vesicles