The Renin-Angiotensin system and SARS-CoV-2 infection: A role for the ACE2 receptor?

Abstract

Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). The renin-angiotensin-aldosterone system (RAAS) has been the focus of research for decades because of its critical role in the physiology of the circulation and the pathophysiology of cardiovascular disease. However, it plays an important role in regulating multiple organs and functions in other tissues including the lung, kidney and heart, together with involvement in the inflammatory response. Early research identified angiotensin-converting enzyme (ACE), a protease which cleaves angiotensin (Ang) I to produce Ang II, the key effector peptide of the RAAS. However, in 2000, a second ACE, ACE2, was discovered which primarily metabolises Ang II into Ang-(1–9). Ang-(1–9) is subsequently converted by neutral endopeptidase and ACE to Ang-(1–7), a vasodilatory peptide. Extensive investigations of ACE2 have revealed that it is widely distributed primarily on lung alveolar epithelial cells, small intestinal enterocytes and vascular endothelial cells in many organs including liver, kidney and brain,1 with multiple additional actions including antiproliferative and antifibrotic effects and, more recently, a role of viral receptor and amino acid transporter.2 Studies with coronaviruses such as severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome coronavirus showed that these viruses relied on a viral spike protein to bind host cell surface receptors for entry into cells. SARS-CoV and SARSCoV-2 both encode similar large-spike proteins with 76% sequence identity. Molecular modelling has shown structural similarity between the receptor binding domains of SARS-CoV and SARS-CoV-2 despite amino acid mutations of the SARS-CoV-2 receptor binding domain.3 It has now been demonstrated that the receptor binding domain in the spike protein interacts with high affinity with ACE2.4–6 By analogy with the SARS virus, SARS-CoV-2 will downregulate cellular expression of ACE2, resulting from endocytosis of the ACE2-SARS-CoV-2 complex, which is essential for infection, activation of ADAM metallopeptidase domain 17, a coregulator of ACE2, and shedding of ACE2 from the cell membrane (Figure 1). Novel antibodies and therapeutic peptides are being developed to interact with the SARS-CoV-2 receptor binding domain and block its interaction with ACE2. An alternative approach is the use of peptides derived from SARS-CoV-2 and ACE2. Interestingly, a peptide composed of two ACE2 motifs (aa22-44 and 351-357) linked by glycine exhibited potent anti-SARS activity.7 Other targets to control viral replication include proteases (3CLpro and PLpro) that process the polypeptide translation product from the genomic RNA into the structural and nonstructural protein components vital for replication of new viruses.3 On theoretical grounds, blockade of ACE2 could confer anti-infective properties against SARS-CoV-2 by preventing entry of the virus into lung pneumocytes. Several small-molecule ACE2 inhibitors have been synthesised,8 of which MLN-4760 has been investigated in animal models.9 Studies with inhibitors confirm predictions from gene-deletion studies that ACE2 is a critical regulator of cardiovascular function,10 counterbalancing the effects of Ang II, and protects against adverse structural changes after tissue injury, mediated by matrix metalloproteinases, free radical production and upregulation of proinflammatory cytokines. ACE2 in the kidney protects against glomerular injury in animal models of renal disease including diabetic nephropathy, and pharmacological inhibition of ACE2 exacerbates kidney damage.2 ACE2 also appears to attenuate the inflammatory response and oxidative stress in models of acute lung injury.2 Thus, any theoretical benefits of ACE2 inhibitors in coronavirus infection would likely be offset by multiple adverse effects on a number of organs and tissues. The Renin-Angiotensin system and SARS-CoV-2 infection: A role for the ACE2 receptor?