Targeting LOX-1 in atherosclerosis and vasculopathy: current knowledge and future perspectives.
Kunming TianSayoko OguraPeter J LittleJianping WengTatsuya SawamuraPublished in: Annals of the New York Academy of Sciences (2018)
LOX-1 (lectin-like oxidized low-density lipoprotein receptor-1; also known as OLR1) is the dominant receptor that recognizes and internalizes oxidized low-density lipoproteins (ox-LDLs) in endothelial cells. Several genetic variants of LOX-1 are associated with the risk and severity of coronary artery disease. The LOX-1-ox-LDL interaction induces endothelial dysfunction, leukocyte adhesion, macrophage-derived foam cell formation, smooth muscle cell proliferation and migration, and platelet activation. LOX-1 activation eventually leads to the rupture of atherosclerotic plaques and acute cardiovascular events. In addition, LOX-1 can be cleaved to generate soluble LOX-1 (sLOX-1), which is a useful diagnostic and prognostic marker for atherosclerosis-related diseases in human patients. Of therapeutic relevance, several natural products and clinically used drugs have emerged as LOX-1 inhibitors that have antiatherosclerotic actions. We hereby provide an updated overview of role of LOX-1 in atherosclerosis and associated vascular diseases, with an aim to highlighting the potential of LOX-1 as a novel theranostic tool for cardiovascular disease prevention and treatment.
Keyphrases
- low density lipoprotein
- cardiovascular disease
- cardiovascular events
- coronary artery disease
- endothelial cells
- smooth muscle
- healthcare
- single cell
- type diabetes
- adipose tissue
- liver failure
- mesenchymal stem cells
- stem cells
- newly diagnosed
- pseudomonas aeruginosa
- ejection fraction
- percutaneous coronary intervention
- photodynamic therapy
- metabolic syndrome
- aortic valve
- drug induced
- binding protein
- bone marrow
- acute coronary syndrome
- left ventricular
- extracorporeal membrane oxygenation
- transcatheter aortic valve replacement
- aortic stenosis
- combination therapy