| Title |
Influence of simvastatin and pravastatin on the biophysical properties of model lipid bilayers and plasma membranes of live cells / |
| Authors |
Polita, Artūras ; Bagdonaitė, Rūta ; Shivabalan, Arun Prabha ; Valinčius, Gintaras |
| DOI |
10.1021/acsbiomaterials.4c00911 |
| Full Text |
|
| Is Part of |
ACS biomaterials science and engineering.. Washington : American Chemical Society. 2024, vol. 10, iss. 9, p. 5714-5722.. eISSN 2373-9878 |
| Keywords [eng] |
BODIPY ; FLIM ; lipid order ; model lipid bilayers ; pravastatin ; simvastatin ; viscosity |
| Abstract [eng] |
Statins are among the most widely used drugs for the inhibition of cholesterol biosynthesis, prevention of cardiovascular diseases, and treatment of hypercholesterolemia. Additionally, statins also exhibit cholesterol-independent benefits in various diseases, including neuroprotective properties in Alzheimer’s disease, anti-inflammatory effects in coronary artery disease, and antiproliferative activities in cancer, which likely result from the statins’ interaction and alteration of lipid bilayers. However, the membrane-modulatory effects of statins and the mechanisms by which statins alter lipid bilayers remain poorly understood. In this work, we explore the membrane-modulating effects of statins on model lipid bilayers and live cells. Through the use of fluorescence lifetime imaging microscopy (FLIM) combined with viscosity-sensitive environmental probes, we demonstrate that hydrophobic, but not hydrophilic, statins are capable of changing the microviscosity and lipid order in model and live cell membranes. Furthermore, we show that hydrophobic simvastatin is capable of forming nanoscale cholesterol-rich domains and homogenizing the cholesterol concentrations in lipid bilayers. Our results provide a mechanistic framework for understanding the bimodal effects of simvastatin on the lipid order and the lateral organization of cholesterol in lipid bilayers. Finally, we demonstrate that simvastatin temporarily decreases the microviscosity of live cell plasma membranes, making them more permeable and increasing the level of intracellular chemotherapeutic drug accumulation. |
| Published |
Washington : American Chemical Society |
| Type |
Journal article |
| Language |
English |
| Publication date |
2024 |
| CC license |
|
