| Literature DB >> 33659546 |
Diantha Van De Vlekkert1, Xiaohiu Qiu1, Ida Annunziata1, Alessandra d'Azzo1.
Abstract
Exosomes are dynamic nanovesicles secreted by virtually all cells and are present in all biological fluids. Given their highly heterogeneous content exosomes have been implicated in many physiological and pathological processes that they exert by influencing cell-cell and cell-ECM communication. In recent years an increasing number of methods have been established for the purification and characterization of exosomes. These include ultracentrifugation, ultrafiltration, size exclusion chromatography, immune capture and precipitation using a proprietary polymer. Here, we provide a protocol based on differential ultracentrifugation and sucrose density gradients tailored for the isolation of crude and ultra-pure exosomes from primary fibroblast cultures derived from adult mouse skeletal muscle. This protocol can be adapted and modified for the isolation and characterization of exosomes from a variety of tissues and bodily fluids.Entities:
Keywords: Cell culture; Exosomes; Fibroblasts; Sucrose gradient; Ultracentrifugation; Western blot
Year: 2020 PMID: 33659546 PMCID: PMC7842540 DOI: 10.21769/BioProtoc.3576
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325