“…These insults lead to a dysfunctional endothelium and inflammatory process in which the EC-derived foam cells express more of new CAM and synthesize EC-factors that attract and induce migration of plasma inflammatory cells, such as monocytes and T lymphocytes to the subendothelium (Simionescu & Antohe, 2006); however, ECs maintain some of their specific attributes, such as Weibel-Palade bodies, intercellular junctions and caveolae (Sima et al, 2009). Infiltration of atherogenic Lps, monocytes and T lymphocytes within the subendothelium start the atherogenetic process both in animal models and in humans (Lawson & Wolf, 2009;Simionescu & Antohe, 2006;Williams & Tabas, 2005). In late stages of atherosclerosis, all cellular components of the plaque, ECs, VSMCs and macrophages, accumulate considerable number of lipid droplets and exhibit the foam cell characteristics (Sima et al, 2009).…”