Angiotensin II induces apoptosis of human right and left ventricular endocardial endothelial cells by activating the AT 2 receptor 1

• Published in: Canadian journal of physiology and pharmacology 2019-02, p.1
• Main Authors: Jacques, Danielle, Provost, Chantale, Normand, Alexandre, Abou Abdallah, Nadia, Al-Khoury, Johny, Bkaily, Ghassan
• Format: Article
• Language: English
• ISSN: 1205-7541

Endocardial endothelial cells (EECs) form a monolayer lining the ventricular cavities. Studies from our laboratory and the literature have shown differences between EECs isolated from the right and left ventricles (EECRs and EECLs, respectively). Angiotensin II (Ang II) was shown to induce apoptosis of different cell types mainly via AT receptor activation. In this study, we verified whether Ang II induces apoptosis of human EECRs and EECLs (hEECRs and hEECLs, respectively) and via which type of receptor. Using the annexin V labeling and in situ TUNEL assays, our results showed that Ang II induced apoptosis of both hEECRs and hEECLs in a concentration-dependent manner. Our results using specific AT and AT receptor antagonists showed that the Ang-II-induced apoptosis in both hEECRs and hEECLs is mediated mainly via the AT receptor. However, AT receptor blockade partially prevented Ang-II-induced apoptosis, particularly in hEECRs. Hence, our results suggest that mainly AT receptors mediate Ang-II-induced apoptosis of hEECRs and hEECLs. The damage of EECs would affect their function as a physical barrier between the blood and cardiomyocytes, thus affecting cardiomyocyte functions.