(TKP2021-EGA-23) Támogató: Innovációs és Technológiai Minisztérium
Nemzeti Kardiovaszkuláris Laboratórium(RRF-2.3.1-21-2022-00003) Támogató: NKFIH
(2019-2.1.7-ERA-NET-2021-00015)
Extracellular vesicles (EVs) are emerging as key factors in maintaining cellular homeostasis,
critical mediators of intercellular communication, potential biomarkers, and therapeutic
tools. While small EVs have been extensively characterized, the molecular signatures
of large EVs (including those generated during regulated cell death pathways) remain
poorly defined. Here, we investigated the characteristics of large EVs released during
apoptosis and pyroptosis by human monocytic cell lines (THP-1 and U937). Apoptosis
was induced by staurosporine and blocked using the pan-caspase inhibitor Q-VD-OPh,
whereas pyroptosis was triggered by LPS/nigericin and inhibited with a selective NLRP3
inhibitor. We found that both forms of regulated cell death markedly enhanced the
release of large EVs. Both apoptotic and pyroptotic large EVs showed increased Annexin
V binding and decreased CD9 expression compared with those released by healthy cells.
Large EVs derived from apoptotic and pyroptotic cells exhibited distinct proteomic
profiles. Pyroptotic large EVs carried interacting protein networks of RNA-binding
proteins and chromatin-associated proteins many of which are known damage-associated
molecular patterns or alarmins. In contrast, we found that a subpopulation of apoptotic
large EVs was characterized by the presence of dsDNA, and active caspase-3/7. Together,
our data shed light on the specific protein cargo of large EVs released by cells during
apoptosis and pyroptosis. This study identifies candidate markers of large EVs released
by dying cells and may enhance our understanding of the role of EVs in regulated cell
death.