Extracellular vesicles (EV) are small lipid bilayer-bound nanoparticles released by a multitude of different cell types in homeostatic and disease states, acting as messengers in cell-cell and cell-matrix communication as well as in tissue-level signaling. In cardiovascular disease, EVs derived from patient blood samples have been identified as a potent asset bearing both diagnostic and prognostic value. With a distinct signature of surface marker proteins and molecular cargo, specific EV populations found in serum can improve the diagnosis of early stages of cardiac or vascular dysfunction preceding irreversible damage, thus improving disease management.
Standardization of this novel and open EV research field will be crucial in translating experimental results into standard clinical practice. Given the dynamics of serum EV release and degradation, along with the varying EV isolation and purification techniques currently applied in EV research, discoveries on serum-derived EVs still face significant limitations regarding reproducibility and clinical practicability. This Methods Collection aims to contribute to the standardization of serum-derived EV research with a particular focus on the role of serum EVs in cardiovascular diseases encompassing but not limited to acute coronary syndrome, heart failure, and inflammatory or calcific valve disease.
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Cited by 1
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2025
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Gabriel Jakob Trauner*1, Dominika Bernath-Nagy*1,2, Melek Sükran Kalinyaprak1, Sabine Merker3, Marcin Luzarowski3, Florian Leuschner1,4, Norbert Frey1,4, Evangelos Giannitsis1, Jona Benjamin Krohn1,4
1Department of Cardiology, Angiology and Pulmonology, University Hospital Heidelberg, 2Heart and Vascular Center, Semmelweis University, 3Core Facility for Mass Spectrometry and Proteomics, Centre for Molecular Biology at Heidelberg University (ZMBH), 4German Centre for Cardiovascular Research (DZHK), Partner site Heidelberg/Mannheim