From the Department of Physiology (M.G., A.V., G.Y.O.).
Mazankowski Alberta Heart Institute, University of Alberta, Edmonton, Canada (M.G., K.W., A.V., Q.N., G.Y.O.).
Circ Res. 2020 May 8;126(10):1456-1474. doi: 10.1161/CIRCRESAHA.120.317015. Epub 2020 Apr 8.
ACE2 (angiotensin-converting enzyme 2) has a multiplicity of physiological roles that revolve around its trivalent function: a negative regulator of the renin-angiotensin system, facilitator of amino acid transport, and the severe acute respiratory syndrome-coronavirus (SARS-CoV) and SARS-CoV-2 receptor. is widely expressed, including, in the lungs, cardiovascular system, gut, kidneys, central nervous system, and adipose tissue. ACE2 has recently been identified as the SARS-CoV-2 receptor, the infective agent responsible for coronavirus disease 2019, providing a critical link between immunity, inflammation, ACE2, and cardiovascular disease. Although sharing a close evolutionary relationship with SARS-CoV, the receptor-binding domain of SARS-CoV-2 differs in several key amino acid residues, allowing for stronger binding affinity with the human ACE2 receptor, which may account for the greater pathogenicity of SARS-CoV-2. The loss of ACE2 function following binding by SARS-CoV-2 is driven by endocytosis and activation of proteolytic cleavage and processing. The ACE2 system is a critical protective pathway against heart failure with reduced and preserved ejection fraction including, myocardial infarction and hypertension, and against lung disease and diabetes mellitus. The control of gut dysbiosis and vascular permeability by ACE2 has emerged as an essential mechanism of pulmonary hypertension and diabetic cardiovascular complications. Recombinant ACE2, gene-delivery of , Ang 1-7 analogs, and Mas receptor agonists enhance ACE2 action and serve as potential therapies for disease conditions associated with an activated renin-angiotensin system. rhACE2 (recombinant human ACE2) has completed clinical trials and efficiently lowered or increased plasma angiotensin II and angiotensin 1-7 levels, respectively. Our review summarizes the progress over the past 20 years, highlighting the critical role of ACE2 as the novel SARS-CoV-2 receptor and as the negative regulator of the renin-angiotensin system, together with implications for the coronavirus disease 2019 pandemic and associated cardiovascular diseases.
ACE2(血管紧张素转换酶 2)具有多方面的生理功能,这些功能围绕着其三重功能展开:肾素-血管紧张素系统的负调节剂、氨基酸转运的促进剂,以及严重急性呼吸系统综合征冠状病毒(SARS-CoV)和 SARS-CoV-2 的受体。ACE2 广泛表达,包括肺部、心血管系统、肠道、肾脏、中枢神经系统和脂肪组织。ACE2 最近被确定为 SARS-CoV-2 的受体,即导致 2019 年冠状病毒病的传染性病原体,为免疫、炎症、ACE2 和心血管疾病之间提供了关键联系。尽管与 SARS-CoV 具有密切的进化关系,但 SARS-CoV-2 的受体结合域在几个关键氨基酸残基上存在差异,使其与人类 ACE2 受体具有更强的结合亲和力,这可能是 SARS-CoV-2 致病性更强的原因。SARS-CoV-2 结合后 ACE2 功能的丧失是由内吞作用和蛋白水解切割及加工的激活驱动的。ACE2 系统是一种关键的保护途径,可预防射血分数降低和保留的心力衰竭、心肌梗死和高血压以及肺部疾病和糖尿病。ACE2 对肠道菌群失调和血管通透性的控制已成为肺动脉高压和糖尿病心血管并发症的重要机制。ACE2 的重组、基因传递、Ang 1-7 类似物和 Mas 受体激动剂增强 ACE2 的作用,可作为与激活的肾素-血管紧张素系统相关的疾病的潜在治疗方法。rhACE2(重组人 ACE2)已完成临床试验,分别有效地降低或增加了血浆血管紧张素 II 和血管紧张素 1-7 的水平。我们的综述总结了过去 20 年的进展,强调了 ACE2 作为新型 SARS-CoV-2 受体和肾素-血管紧张素系统负调节剂的关键作用,以及其对 2019 年冠状病毒病大流行和相关心血管疾病的影响。