» Articles » PMID: 39452140

Unveiling the Interplay-Vitamin D and ACE-2 Molecular Interactions in Mitigating Complications and Deaths from SARS-CoV-2

Overview
Journal Biology (Basel)
Publisher MDPI
Specialty Biology
Date 2024 Oct 25
PMID 39452140
Authors
Affiliations
Soon will be listed here.
Abstract

The interaction of the SARS-CoV-2 spike protein with membrane-bound angiotensin-converting enzyme-2 (ACE-2) receptors in epithelial cells facilitates viral entry into human cells. Despite this, ACE-2 exerts significant protective effects against coronaviruses by neutralizing viruses in circulation and mitigating inflammation. While SARS-CoV-2 reduces ACE-2 expression, vitamin D increases it, counteracting the virus's harmful effects. Vitamin D's beneficial actions are mediated through complex molecular mechanisms involving innate and adaptive immune systems. Meanwhile, vitamin D status [25(OH)D concentration] is inversely correlated with severity, complications, and mortality rates from COVID-19. This study explores mechanisms through which vitamin D inhibits SARS-CoV-2 replication, including the suppression of transcription enzymes, reduced inflammation and oxidative stress, and increased expression of neutralizing antibodies and antimicrobial peptides. Both hypovitaminosis D and SARS-CoV-2 elevate renin levels, the rate-limiting step in the renin-angiotensin-aldosterone system (RAS); it increases ACE-1 but reduces ACE-2 expression. This imbalance leads to elevated levels of the pro-inflammatory, pro-coagulatory, and vasoconstricting peptide angiotensin-II (Ang-II), leading to widespread inflammation. It also causes increased membrane permeability, allowing fluid and viruses to infiltrate soft tissues, lungs, and the vascular system. In contrast, sufficient vitamin D levels suppress renin expression, reducing RAS activity, lowering ACE-1, and increasing ACE-2 levels. ACE-2 cleaves Ang-II to generate Ang, a vasodilatory, anti-inflammatory, and anti-thrombotic peptide that mitigates oxidative stress and counteracts the harmful effects of SARS-CoV-2. Excess ACE-2 molecules spill into the bloodstream as soluble receptors, neutralizing and facilitating the destruction of the virus. These combined mechanisms reduce viral replication, load, and spread. Hence, vitamin D facilitates rapid recovery and minimizes transmission to others. Overall, vitamin D enhances the immune response and counteracts the pathological effects of SARS-CoV-2. Additionally, data suggests that widely used anti-hypertensive agents-angiotensin receptor blockers and ACE inhibitors-may lessen the adverse impacts of SARS-CoV-2, although they are less potent than vitamin D.

Citing Articles

Vitamin D Deficiency Meets Hill's Criteria for Causation in SARS-CoV-2 Susceptibility, Complications, and Mortality: A Systematic Review.

Wimalawansa S Nutrients. 2025; 17(3).

PMID: 39940457 PMC: 11820523. DOI: 10.3390/nu17030599.


Nerve Growth Factor and Brain-Derived Neurotrophic Factor in COVID-19.

Petrella C, Ferraguti G, Tarani L, Tarani F, Messina M, Fiore M Biology (Basel). 2024; 13(11).

PMID: 39596862 PMC: 11591877. DOI: 10.3390/biology13110907.

References
1.
Michigami T . [Rickets/Osteomalacia. Consensus on Vitamin D Deficiency and Insufficiency in Children.]. Clin Calcium. 2018; 28(10):1307-1311. DOI: CliCa181013071311. View

2.
Koivisto O, Hanel A, Carlberg C . Key Vitamin D Target Genes with Functions in the Immune System. Nutrients. 2020; 12(4). PMC: 7230898. DOI: 10.3390/nu12041140. View

3.
Shoemaker M, Huynh L, Smith C, Mustad V, Duarte M, Cramer J . Immunomodulatory Effects of Vitamin D and Prevention of Respiratory Tract Infections and COVID-19. Top Clin Nutr. 2022; 37(3):203-217. PMC: 9222791. DOI: 10.1097/TIN.0000000000000284. View

4.
Zhou P, Yang X, Wang X, Hu B, Zhang L, Zhang W . A pneumonia outbreak associated with a new coronavirus of probable bat origin. Nature. 2020; 579(7798):270-273. PMC: 7095418. DOI: 10.1038/s41586-020-2012-7. View

5.
Gimenez V, Inserra F, Ferder L, Garcia J, Manucha W . Vitamin D deficiency in African Americans is associated with a high risk of severe disease and mortality by SARS-CoV-2. J Hum Hypertens. 2020; 35(4):378-380. PMC: 7425793. DOI: 10.1038/s41371-020-00398-z. View