Ethanol Enhances Endothelial Rigidity by Targeting VE-Cadherin-Implications for Acute Aortic Dissection

• Published in: Journal of clinical medicine 2023-07, Vol.12 (15), p.4967
• Main Authors: Mulorz, Joscha, Ibing, Wiebke, Cappallo, Melanie, Braß, Sönke Maximilian, Takeuchi, Kiku, Raaz, Uwe, Schellinger, Isabel Nahal, Krott, Kim Jürgen, Schelzig, Hubert, Aubin, Hug, Oberhuber, Alexander, Elvers, Margitta, Wagenhäuser, Markus Udo
• Format: Article
• Language: English
• Subjects: Alcohol; Alcohol, Denatured; Aortic dissection; Cadherins; Cell culture; Cell growth; Clinical medicine; Development and progression; Dissecting aneurysm; Epithelial cells; Health aspects; Manufacturers; Membranes; Permeability; Polyethylene terephthalate; Proteins; Risk factors; Vascular endothelium
• ISSN: 2077-0383; 2077-0383
• DOI: 10.3390/jcm12154967

(1) Background: Acute aortic dissection (AAD) is caused by an endothelial entry tear followed by intimomedial delamination of the outer layers of the vessel wall. The established risk factors include hypertension and smoking. Another rising candidate risk factor is excessive alcohol consumption. This experimental study explores the effects of nicotine (Nic), angiotensin II (Ang II), and ethanol (EtOH) on human aortic endothelial cells (hAoEC). (2) Methods: HAoECs were exposed to Nic, Ang II, and EtOH at different dose levels. Cell migration was studied using the scratch assay and live-cell imaging. The metabolic viability and permeability capacity was investigated using the water-soluble tetrazolium (WST)-1 assay and an in vitro vascular permeability assay. Cell adherence was studied by utilizing the hanging drop assay. The transcriptional and protein level changes were analyzed by RT-qPCR, Western blotting and immunohistochemistry for major junctional complexing proteins. (3) Results: We observed reduced metabolic viability following Ang II and EtOH exposure vs. control. Further, cell adherence was enhanced by EtOH exposure prior to trituration and by all risk factors after trituration, which correlated with the increased gene and protein expression of VE-cadherin upon EtOH exposure. The cell migration capacity was reduced upon EtOH exposure vs. controls. (4) Conclusion: Marked functional changes were observed upon exposure to established and potential risk factors for AAD development in hAoECs. Our findings advocate for an enhanced mechanical rigidity in hAoECs in response to the three substances studied, which in turn might increase endothelial rigidity, suggesting a novel mechanism for developing an endothelial entry tear due to reduced deformability in response to increased shear and pulsatile stress.