High stretch induces endothelial dysfunction accompanied by oxidative stress and actin remodeling in human saphenous vein endothelial cells

• Published in: Scientific reports Vol. 11; no. 1; p. 13493
• Main Authors: Girão-Silva, T., Fonseca-Alaniz, M. H., Ribeiro-Silva, J. C., Lee, J., Patil, N. P., Dallan, L. A., Baker, A. B., Harmsen, M. C., Krieger, J. E., Miyakawa, A. A.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 29-06-2021; Nature Publishing Group; Nature Portfolio
• Subjects: 631/80; 631/80/86; 692/4019; 692/4019/592; Acetylcysteine; Actin; Adhesion; Antioxidants; Bioavailability; Cell adhesion; Cofilin; Coronary artery; Cytoskeleton; E-selectin; Endothelial cells; Heart surgery; Humanities and Social Sciences; Inflammation; multidisciplinary; Oxidative stress; Science; Science (multidisciplinary); Veins & arteries
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-021-93081-3

The rate of the remodeling of the arterialized saphenous vein conduit limits the outcomes of coronary artery bypass graft surgery (CABG), which may be influenced by endothelial dysfunction. We tested the hypothesis that high stretch (HS) induces human saphenous vein endothelial cell (hSVEC) dysfunction and examined candidate underlying mechanisms. Our results showed that in vitro HS reduces NO bioavailability, increases inflammatory adhesion molecule expression (E-selectin and VCAM1) and THP-1 cell adhesion. HS decreases F-actin in hSVECs, but not in human arterial endothelial cells, and is accompanied by G-actin and cofilin’s nuclear shuttling and increased reactive oxidative species (ROS). Pre-treatment with the broad-acting antioxidant N-acetylcysteine (NAC) supported this observation and diminished stretch-induced actin remodeling and inflammatory adhesive molecule expression. Altogether, we provide evidence that increased oxidative stress and actin cytoskeleton remodeling play a role in HS-induced saphenous vein endothelial cell dysfunction, which may contribute to predisposing saphenous vein graft to failure.