Lipoprotein-matrix interactions play an important role in arterial disease.
Extracellular matrix proteoglycans bind and retain specific positively cha
rged domains on apolipoproteins B- and E-containing lipoproteins during ath
erogenesis. Retained lipoproteins can undergo several modifications, which
may alter their interaction with extracellular matrix molecules. Growth fac
tors, cytokines and oxidized low density lipoproteins influence proteoglyca
n structure, rendering them more likely to bind and retain lipoproteins dur
ing atherogenesis. Lipoproteins, native and modified, also can modulate the
expression of several of the matrix degrading enzymes present in vascular
tissue, thereby influencing plague stability. Thus, the interaction of athe
rogenic lipoproteins with arterial wail matrix molecules can influence the
genesis and progression of atherosclerosis and its complications. Curr Opin
Lipidol 11:457-463. (C) 2000 Lippincott Williams & Wilkins.