The ability of the metalloproteinases to degrade extracellular matrix
proteins is essential for the matrix remodelling that occurs during in
filtration of inflammatory cells, intimal thickening, angiogenesis and
plaque rupture which are a result of atherosclerosis. Increased metal
loproteinase activity therefore requires stimulation of metalloprotein
ase expression by cytokines and growth factors, activation of metallop
roteinases, and downregulation of tissue inhibitors of metalloproteina
ses. In addition, metalloproteinases may influence atherosclerosis by
processing of proteins involved in inflammation and cell growth and de
ath and the tissue inhibitors of metalloproteinases may also play a le
ss inhibitory role by influencing cell growth and apoptosis. Curr Opin
Lipidol 9:413-423. (C) 1998 Lippincott Williams & Wilkins