4.7 Article

Modulation of the Circulating Extracellular Vesicles in Response to Different Exercise Regimens and Study of Their Inflammatory Effects

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MDPI
DOI: 10.3390/ijms24033039

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extracellular vesicles; aerobic exercise; aerobic training; exerkines; myokines; miRNA expression

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Exercise-released extracellular vesicles (EVs) are a new class of exerkines that promote systemic beneficial effects. Differences in exercise protocols and the lack of standardized EV isolation protocols make it difficult to compare studies in the literature. This study investigated the release of EVs and associated miRNAs in response to different exercise regimens, finding increases in EVs and specific miRNAs following acute aerobic exercise (AAE). The results provide a better understanding of the role of circulating EVs in exercise-induced inflammatory processes.
Exercise-released extracellular vesicles (EVs) are emerging as a novel class of exerkines that promotes systemic beneficial effects. However, slight differences in the applied exercise protocols in terms of mode, intensity and duration, as well as the need for standardized protocols for EV isolation, make the comparison of the studies in the literature extremely difficult. This work aims to investigate the EV amount and EV-associated miRNAs released in circulation in response to different physical exercise regimens. Healthy individuals were subjected to different exercise protocols: acute aerobic exercise (AAE) and training (AT), acute maximal aerobic exercise (AMAE) and altitude aerobic training (AAT). We found a tendency for total EVs to increase in the sedentary condition compared to trained participants following AAE. Moreover, the cytofluorimetric analysis showed an increase in CD81(+)/SGCA(+)/CD45(-) EVs in response to AAE. Although a single bout of moderate/maximal exercise did not impact the total EV number, EV-miRNA levels were affected as a result. In detail, EV-associated miR-206, miR-133b and miR-146a were upregulated following AAE, and this trend appeared intensity-dependent. Finally, THP-1 macrophage treatment with exercise-derived EVs induced an increase of the mRNAs encoding for IL-1 beta, IL-6 and CD163 using baseline and immediately post-exercise EVs. Still, 1 h post-exercise EVs failed to stimulate a pro-inflammatory program. In conclusion, the reported data provide a better understanding of the release of circulating EVs and their role as mediators of the inflammatory processes associated with exercise.

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