Both lipoproteins and the endothelium play critical roles in the initiation
and progression of atherosclerosis. An understanding of the interactions b
etween lipoproteins and the endothelium facilitates our understanding of at
herogenesis and could suggest new therapeutic targets. Lipoproteins have im
portant effects on endothelial cells. Atherogenic lipoproteins such as remn
ants, low-density lipoprotein (LDL), and oxidized LDL act on endothelial ce
lls to cause upregulation of endothelial adhesion molecules and selectins,
promotion of oxygen radicals, increased apoptosis, and reduced endothelium-
dependent relaxation. Antiatherogenic lipoproteins such as HDL protect endo
thelial cells from oxidative stress and apoptosis and reduce adhesion molec
ule expression. Conversely, the endothelium has major effects on lipoprotei
n metabolism and function. Several lipases, including lipoprotein lipase, h
epatic lipase, endothelial lipase, and secretory phospholipase A2, are boun
d to the endothelial cell matrix and have the ability to hydrolyze lipoprot
ein triglycerides and phospholipids. Furthermore, endothelial cells express
a variety of lipoprotein receptors including the VLDL receptor, scavenger
receptor A, SR-BI, CD36, and LOX-1, although little is known about their fu
nction on endothelial cells. Although a great deal is known about endotheli
al-lipoprotein interactions, more research is needed in this important area
.