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1.
Biochem Soc Trans ; 47(2): 509-516, 2019 04 30.
Article in English | MEDLINE | ID: mdl-30952802

ABSTRACT

Apoptosis is an essential process for normal physiology and plays a key role in the resolution of inflammation. Clearance of apoptotic cells (ACs) involves complex signalling between phagocytic cells, ACs, and the extracellular vesicles (EVs) they produce. Here, we discuss apoptotic cell-derived extracellular vesicles (ACdEVs) and how their structure relates to their function in AC clearance and the control of inflammation, focussing on the ACdEV proteome. We review the current knowledge, ongoing work and future directions for research in this field.


Subject(s)
Apoptosis/physiology , Extracellular Vesicles/metabolism , Animals , Apoptosis/genetics , Humans , Inflammation/metabolism , Macrophages/metabolism , Phagocytosis/physiology , Proteome/metabolism , Signal Transduction/physiology , Structure-Activity Relationship
2.
Sci Rep ; 8(1): 5730, 2018 04 10.
Article in English | MEDLINE | ID: mdl-29636530

ABSTRACT

Extracellular vesicles (EVs) have important roles in physiology, pathology, and more recently have been identified as efficient carriers of therapeutic cargoes. For efficient study of EVs, a single-step, rapid and scalable isolation strategy is necessary. Chromatography techniques are widely used for isolation of biological material for clinical applications and as EVs have a net negative charge, anion exchange chromatography (AIEX) is a strong candidate for column based EV isolation. We isolated EVs by AIEX and compared them to EVs isolated by ultracentrifugation (UC) and tangential flow filtration (TFF). EVs isolated by AIEX had comparable yield, EV marker presence, size and morphology to those isolated by UC and had decreased protein and debris contamination as compared to TFF purified EVs. An improved AIEX protocol allowing for higher flow rates and step elution isolated 2.4*1011 EVs from 1 litre of cell culture supernatant within 3 hours and removed multiple contaminating proteins. Importantly AIEX isolated EVs from different cell lines including HEK293T, H1299, HCT116 and Expi293F cells. The AIEX protocol described here can be used to isolate and enrich intact EVs in a rapid and scalable manner and shows great promise for further use in the field for both research and clinical purposes.


Subject(s)
Cell Fractionation , Chromatography, Ion Exchange , Extracellular Vesicles , Subcellular Fractions , Cell Fractionation/methods , Chromatography, Ion Exchange/methods , Filtration , Humans , Ultracentrifugation
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