1*Stankova, T.R., 1Stefanova, K.I., 1Delcheva, G.T. & 1 Maneva, A.I.
The development of atherosclerosis is a multifactorial process, but oxidized low-density lipoprotein (oxLDL) has been recognized as a critical player in the pathogenesis of the disease. The lectin-like oxLDL receptor-1 (LOX-1) has recently been identified as the primary scavenger receptor of oxLDL, which mediates their detrimental biological effects in endothelial cells. Subsequent studies have revealed that LOX-1 is also expressed by other cells highly implicated in atherosclerosis, such as monocytes/macrophages, vascular smooth muscle cells, cardiomyocytes and platelets. On one hand interaction of oxLDL with LOX-1 promotes oxidative stress and transcription of pro-inflammatory molecules, and on the other hand increases the expression of LOX-1 as a result of the vicious cycle, activated by the atherogens. Thus, LOX-1 has been suggested as a key molecule in vascular inflammation and in atherosclerotic plaque formation, destabilization, erosion and rupture.
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