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A three-step approach identifies novel shear stress-sensitive endothelial microRNAs involved in vasculoprotective effects of high-intensity interval training (HIIT).

Authors :
Schmitz B
Breulmann FL
Jubran B
Rolfes F
Thorwesten L
Krüger M
Klose A
Schnittler HJ
Brand SM
Source :
Oncotarget [Oncotarget] 2019 Jun 04; Vol. 10 (38), pp. 3625-3640. Date of Electronic Publication: 2019 Jun 04 (Print Publication: 2019).
Publication Year :
2019

Abstract

Circulatory microRNAs (c-miRNAs) are regulated in response to physical activity and may exert anti-atherosclerotic effects. Since the vascular endothelium is an abundant source of c-miRNAs, we aimed to identify novel vasculoprotective exercise-induced c-miRNAs by the combined analysis of published endothelial miRNA array data followed by in vivo and in vitro validation. We identified 8 different array-based publications reporting 185 endothelial shear stress-regulated miRNAs of which 13 were identified in ≥3 independent reports. Nine miRNAs had already been associated with physical activity. Of the remaining novel miRNAs, miR-98-3p and miR-125-5p were selected for further analysis due to reported vasculoprotective effects. Analysis in two different 4-week high-intensity interval training (HIIT) groups (group 1 [n=27]: 4x30 s, group 2 [n=25]: 8x15 s; all-out running) suggested significantly elevated miR-98 and miR-125a-5p levels in response to acute exercise at baseline and at follow-up. Endothelial in vitro shear stress experiments revealed increased miR-125a-5p and miR-98-3p levels in medium of human umbilical vein endothelial cells at 30 dyn/cm <superscript>2</superscript> after 20 and 60 min, respectively. Our results suggest that miR-98-3p and miR-125a-5p can be rapidly secreted by endothelial cells, which might be the source of increased c-miR-98-3p and -125a-5p levels in response to HIIT. Both miRNAs attenuate endothelial inflammation and may mediate vasculoprotective effects of physical exercise including HIIT.<br />Competing Interests: CONFLICTS OF INTEREST No financial or personal relationships exist between any of the authors and other people or organizations that could influence the present study. FUNDING Grants of the German Research Council (DFG) to HS (SCHN 43076-2) and support by the Excellence Cluster Cells In Motion (CIM) flexible fund to HS (FF-2014-15) are also greatly acknowledged. BJ was supported by a scholarship from the ‘Katholischer Akademischer Ausländer-Dienst’ (KAAD).

Details

Language :
English
ISSN :
1949-2553
Volume :
10
Issue :
38
Database :
MEDLINE
Journal :
Oncotarget
Publication Type :
Academic Journal
Accession number :
31217898