Using a static magnetic field to attenuate the severity in COVID-19-invaded lungs.

Publication date: Jul 22, 2024

Two important factors affecting the progress of coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are the S-protein binding function of ACE2 receptors and the membrane fluidity of host cells. This study aimed to evaluate the effect of static magnetic field (SMF) on S-protein/ACE2 binding and cellular membrane fluidity of lung cells, and was performed in vitro using a Calu-3 cell model and in vivo using an animal model. The ability of ACE2 receptors to bind to SARS-CoV-2 spike protein on host cell surfaces under SMF stimulation was evaluated using fluorescence images. Host lung cell membrane fluidity was tested using fluorescence polarization to determine the effects of SMF. Our results indicate that 0. 4 T SMF can affect binding between S-protein and ACE2 receptors and increase Calu-3 cell membrane fluidity, and that SMF exposure attenuates LPS-induced alveolar wall thickening in mice. These results may be of value for developing future non-contact, non-invasive, and low side-effect treatments to reduce disease severity in COVID-19-invaded lungs.

Open Access PDF

Concepts Keywords
Coronavirus ACE2 protein, human
Mice Angiotensin-Converting Enzyme 2
Model Angiotensin-Converting Enzyme 2
Protein Animals
Severe Cell Line
COVID-19
Disease Models, Animal
Humans
Lung
Magnetic Fields
Membrane Fluidity
Mice
Protein Binding
SARS-CoV-2
Spike Glycoprotein, Coronavirus
Spike Glycoprotein, Coronavirus
spike protein, SARS-CoV-2

Original Article

(Visited 3 times, 1 visits today)