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Research explains the role of high cholesterol in SARS-CoV-2 infectivity

Cholesterol lures in coronavirus
ApoE lipids shift ACE2 to an endocytic pathway. A, representative images from dSTORM superresolution imaging. GM1 clusters (yellow) increase dramatically in the presence of blood serum when apoE is present (bottom panel), labeled with CTxB. ACE2 receptor (cyan) labeled with ACE2 antibody has very little overlap (white circle) with GM1 clusters when blood serum is removed (middle panel). The scale bar represents 1 μm. B and C, pair correlation from dSTORM imaging. ACE2 was compared with GM1 lipids (CTxB labeled, B) and phosphatidyl inositol 4,5-bisphosphate (PIP2, C). Loading cells with lipidated apoE (+chol) (dark blue shading) increased the pair correlation with GM1 clusters and decreased the pair correlation with PIP2 clusters. Hence apoE-mediated lipid influx moves ACE2 from PIP2 clusters to GM1 clusters. D, model showing cholesterol-dependent cluster-associated protein activation of ACE2 from PIP2 domains (brown lipids) to endocytic GM1 lipids (dark gray) and enhanced SARS-CoV-2 viral entry. Lipidated apoE is shown bound to low-density lipoprotein receptor (LDLR) (red) and delipidated apoE is shown bound to very low-density lipoprotein receptor (VLDLR). VLDLR facilitates reverse cholesterol transport (RCT). An inset shows the cryo-EM structure (PDB 6M18) of an anionic lipid-binding site (putative PIP2 site) in ACE2. See also supporting information. E, cluster size analysis suggests GM1 clustering is regulated by apoE-mediated lipid transportation between serum and cell membrane. F, ApoE transportation of lipid regulates apparent cluster density. Cholesterol influx from serum results in an increase in number and apparent size. G, ACE2 activity assay was performed to detect ACE2’s expression in wildtype HEK293T cells. Cells incubated with ACE2 inhibitor showed significantly decreased ACE2 activity, suggesting ACE2 is expressed in the HEK293T cells. Data are expressed as mean ± SD, ∗p < 0.05, ∗∗p < 0.01, ∗∗∗∗p < 0.0001, two-sided Student’s t test. H, model for SARS-CoV-2 viral entry in high and low cholesterol. When cholesterol is high, ACE2 translocated to GM1 clusters, a position optimal for viral binding and endocytosis. When cholesterol is low, ACE2 traffics away from GM1 clusters, a position that poorly facilitates viral infection (PIP2 domains not shown). Credit: Journal of Biological Chemistry (2023). DOI: 10.1016/j.jbc.2023.104763

A recent study has unveiled the doorway that SARS-CoV2 uses to slip inside cells undetected.

SARS-CoV-2 uses the receptor angiotensin-converting enzyme 2, or ACE2, to infect . However, this receptor alone does not paint a complete picture of how the virus enters cells. ACE2 is like a doorknob; when SARS-CoV-2 grabs it and maneuvers it precisely, this allows the virus to open a doorway to the cell's interworking and step inside, but the identity of the door has eluded scientists.

Scott Hansen, an associate professor of molecular medicine at the University of Florida Scripps, discovered that cholesterol clusters make up that door. His team published their work in the Journal of Biological Chemistry.

Early on in the COVID-19 pandemic, the elderly and people with such as hypertension, diabetes, Alzheimer's and cardiovascular diseases experienced more viral-related deaths. However, children seemed to be less susceptible.

Hansen hypothesized that part of this phenomenon was due to the high amounts of tissue cholesterol in populations with chronic disease. From 2017 to 2020, 86.4 million U.S. adults age 20 or older had high or borderline high cholesterol in the blood.

After completing studies using cutting-edge technology like super resolution microscopy, his team showed that cholesterol on the makes ACE2 readily accessible to SARS-CoV2 for cell entry.

"Our cells have a protective coat of lipids, or fat, that keeps out invaders and bad molecules," Hansen said. "Cholesterol is a part of a place where nutrients come into the cell. I live in Florida; so we think of this mechanism as, if a hurricane is coming, you batten down the hatches after collecting resources. But this virus is sneaking in when you pull the door closed."

Cholesterol is necessary for survival, but too much cholesterol may be increasing your risk for COVID-19 at the cellular and biochemical levels.

"In smokers with chronic disease, cholesterol in the is elevated two-fold, a magnitude of change that dramatically increases infectivity of the virus in cell culture," Hansen said. In fact, according to a study, supported by the National Heart, Lung, and Blood Institute, smoking was associated with a higher risk of severe COVID-19, including death.

However, Hansen's past research has shown that the cholesterol promoting SARS-CoV-2 infection can easily be disrupted to help patients stay healthy and avoid infection.

"Mechanical force and polyunsaturated fatty acids disrupt the aggregation of the cholesterol," Hansen said. "Healthy is achieved with exercise. In our studies, cells need to be jostled a little bit in order to keep the cholesterol from setting up in the cell membrane. Regular exercise with its increased heart rate and blood flow should reduce the cholesterol aggregates in the cell membranes."

In addition to new insights on the entry mechanism of SARS-CoV-2, Hansen's study also highlighted the inaccuracies of the way doctors assess cholesterol risk in their patients. Currently, the only way to test cholesterol levels is via a blood test.

"Basically, cholesterol goes both ways," Hansen said. "It gets loaded into cells, which is the forward pathway. But then there's reverse cholesterol transport where the body takes cholesterol back out of the cells and moves it to your liver and excretes it out of the body or recycles it. If you measure cholesterol levels in the blood, you don't know the levels in the tissue or if it is being taken out or brought in."

Hansen and his team are working with physicians to come up with a test that more accurately represents tissue cholesterol and its distribution throughout the body.

"In the future, this study may affect how doctors think about cholesterol in the body," Hansen said. "Instead of focusing on the blood, which changes every time you eat, they will need to focus on the tissues and how the is taken up over time. It's a harder measurement, but, in the end, it may help people understand their risk for disease and save lives."

More information: Hao Wang et al, The role of high cholesterol in SARS-CoV-2 infectivity, Journal of Biological Chemistry (2023). DOI: 10.1016/j.jbc.2023.104763

Journal information: Journal of Biological Chemistry
Citation: Research explains the role of high cholesterol in SARS-CoV-2 infectivity (2023, June 20) retrieved 27 April 2024 from https://medicalxpress.com/news/2023-06-role-high-cholesterol-sars-cov-infectivity.html
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