Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2020 Jul;251(3):228-248.
doi: 10.1002/path.5471. Epub 2020 Jun 10.

Angiotensin-converting enzyme 2 (ACE2), SARS-CoV-2 and the pathophysiology of coronavirus disease 2019 (COVID-19)

Affiliations
Review

Angiotensin-converting enzyme 2 (ACE2), SARS-CoV-2 and the pathophysiology of coronavirus disease 2019 (COVID-19)

Arno R Bourgonje et al. J Pathol. 2020 Jul.

Abstract

Angiotensin-converting enzyme 2 (ACE2) has been established as the functional host receptor for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus responsible for the current devastating worldwide pandemic of coronavirus disease 2019 (COVID-19). ACE2 is abundantly expressed in a variety of cells residing in many different human organs. In human physiology, ACE2 is a pivotal counter-regulatory enzyme to ACE by the breakdown of angiotensin II, the central player in the renin-angiotensin-aldosterone system (RAAS) and the main substrate of ACE2. Many factors have been associated with both altered ACE2 expression and COVID-19 severity and progression, including age, sex, ethnicity, medication, and several co-morbidities, such as cardiovascular disease and metabolic syndrome. Although ACE2 is widely distributed in various human tissues and many of its determinants have been well recognised, ACE2-expressing organs do not equally participate in COVID-19 pathophysiology, implying that other mechanisms are involved in orchestrating cellular infection resulting in tissue damage. Reports of pathologic findings in tissue specimens of COVID-19 patients are rapidly emerging and confirm the established role of ACE2 expression and activity in disease pathogenesis. Identifying pathologic changes caused by SARS-CoV-2 infection is crucially important as it has major implications for understanding COVID-19 pathophysiology and the development of evidence-based treatment strategies. Currently, many interventional strategies are being explored in ongoing clinical trials, encompassing many drug classes and strategies, including antiviral drugs, biological response modifiers, and RAAS inhibitors. Ultimately, prevention is key to combat COVID-19 and appropriate measures are being taken accordingly, including development of effective vaccines. In this review, we describe the role of ACE2 in COVID-19 pathophysiology, including factors influencing ACE2 expression and activity in relation to COVID-19 severity. In addition, we discuss the relevant pathological changes resulting from SARS-CoV-2 infection. Finally, we highlight a selection of potential treatment modalities for COVID-19. © 2020 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.

Keywords: angiotensin-converting enzyme 2 (ACE2); coronavirus disease 2019 (COVID-19); organ involvement; pathology; pathophysiology; renin-angiotensin-aldosterone system (RAAS); risk factors; severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2); treatment.

PubMed Disclaimer

Figures

Figure 1
Figure 1
(A–C) Simplified representation of SARS‐CoV‐2 infection and the role of ACE2 in this process. (A) First, SARS‐CoV‐2 may pass through either the mucous membranes, primarily the nasal epithelia, by binding to the ACE2 receptor. (B) In addition, SARS‐CoV‐2 can directly enter the respiratory tract and infect respiratory epithelial cells. After infection, extensive diffuse alveolar damage occurs in the lungs, followed by bilateral oedema, diffuse reactive hyperplasia of type II pneumocytes, thickening of alveolar septa, and infiltration of inflammatory cells. (C) A simplified representation of COVID‐19‐related renal involvement. Typical COVID‐19‐associated changes in the kidneys are diffuse tubular injury with loss of brush border integrity, endothelial damage of the capillaries, and erythrocyte aggregates occluding the capillary lumina.
Figure 2
Figure 2
Structure of the renin‐angiotensin‐aldosterone system (RAAS), the role of ACE2 in this physiological system, and potential treatment targets.
Figure 3
Figure 3
SARS‐CoV‐2 interacts with ACE2 as host cell receptor. In addition to binding, priming of the viral spike (S) protein by the host serine protease TMPRSS2 is required for cell entry.
Figure 4
Figure 4
(A–D) Pathological changes in lungs and kidneys from autopsy specimens of patients with COVID‐19. (A) Thickening of alveolar septa with lymphocytic infiltrate and oedema is observed together with damage and release of alveolar epithelial cells and other cellular debris in alveolar spaces. (B) Alveoli with variable thickening of alveolar walls with partial collagen fibrosis (right upper part) and severe damage with, besides cellular debris, intra‐alveolar oedema, protein, fibrin, and hyaline membranes. (C) Pathological changes in kidneys from an autopsy specimen of a patients with COVID‐19. The proximal convoluted tubules show loss of brush border integrity and vacuolar degeneration. This coincides with debris composed of necrotic epithelium in tubular lumina. Erythrocyte aggregates obstructing peritubular capillaries are frequently present. In some cases, inflammatory infiltrates are present in tubules with multiple foci of bacteria and white blood cell casts. (D) Segmental fibrin thrombi were observed in glomeruli, with ischaemic glomerular contraction with the accumulation of leaked plasma in Bowman’s space.

Similar articles

Cited by

References

    1. Wu Z, McGoogan JM. Characteristics of and important lessons from the coronavirus disease 2019 (COVID‐19) outbreak in China: summary of a report of 72 314 cases from the Chinese Center for Disease Control and Prevention. JAMA 2020; 323 : 1239–1242. - PubMed
    1. Phan LT, Nguyen TV, Luong QC, et al. Importation and human‐to‐human transmission of a novel coronavirus in Vietnam. N Engl J Med 2020; 382 : 872–874. - PMC - PubMed
    1. Report of the WHO–China Joint Mission on Coronavirus Disease 2019 (COVID‐19), 16–24 February 2020 . [Accessed 7 April 2020]. Available from: https://www.who.int/docs/default-source/coronaviruse/who-china-joint-mis...
    1. Lake MA. What we know so far: COVID‐19 current clinical knowledge and research. Clin Med (Lond) 2020; 20 : 124–127. - PMC - PubMed
    1. Phua J, Weng L, Ling L, et al. Intensive care management of COVID/19: challenges and recommendations. Lancet Respir Med 2020; 8 : 506–517. - PMC - PubMed

MeSH terms

LinkOut - more resources