Extracellular vesicles mediate low dose ionizing radiation-induced immune and inflammatory responses in the blood

<p><b>Purpose:</b> Radiation-induced bystander effects (RIBE) imply the involvement of complex signaling mechanisms, which can be mediated by extracellular vesicles (EVs). Using an <i>in vivo</i> model, we investigated EV-transmitted RIBE in blood plasma and radiation effects on plasma EV miRNA profiles.</p> <p><b>Materials and methods:</b> C57Bl/6 mice were total-body irradiated with 0.1 and 2Gy, bone marrow-derived EVs were isolated, and injected systemically into naïve, “bystander” animals. Proteome profiler antibody array membranes were used to detect alterations in plasma, both in directly irradiated and bystander mice. MiRNA profile of plasma EVs was determined by PCR array.</p> <p><b>Results:</b> M-CSF and pentraxin-3 levels were increased in the blood of directly irradiated and bystander mice both after low and high dose irradiations, CXCL16 and lipocalin-2 increased after 2 Gy in directly irradiated and bystander mice, CCL5 and CCL11 changed in bystander mice only. Substantial overlap was found in the cellular pathways regulated by those miRNAs whose level were altered in EVs isolated from the plasma of mice irradiated with 0.1 and 2 Gy. Several of these pathways have already been associated with bystander responses.</p> <p><b>Conclusion:</b> Low and high dose effects overlapped both in EV-mediated alterations in signalling pathways leading to RIBE and in their systemic manifestations.</p>