Arteriosclerosis, Thrombosis, and Vascular Biology. 2002;22:717-726
Published online before print March 14, 2002, doi: 10.1161/01.ATV.0000015598.86369.04
Published online before print March 14, 2002, doi: 10.1161/01.ATV.0000015598.86369.04
© 2002 American Heart Association, Inc.
Brief Reviews |
Pleiotropic Actions of Peroxisome Proliferator–Activated Receptors in Lipid Metabolism and Atherosclerosis
From UR545 INSERM, Département d’Athérosclérose, Institut Pasteur de Lille, and Faculté de Pharmacie, Université de Lille II, Lille, France.
Correspondence to Prof Bart Staels, U545 INSERM, Institut Pasteur de Lille, 1 rue Calmette, BP 245, 59019 Lille Cedex, France. E-mail bart.staels{at}pasteur-lille.fr
Peroxisome proliferator–activated receptors (PPARs) are nuclear receptors activated by fatty acids and derivatives. Although PPAR
mediates the hypolipidemic action of fibrates, PPAR
is the receptor for the antidiabetic glitazones. PPAR is highly expressed in tissues such as liver, muscle, kidney, and heart, where it stimulates the ß-oxidative degradation of fatty acids. PPAR is predominantly expressed in adipose tissues, where it promotes adipocyte differentiation and lipid storage. PPARß/
is expressed in a wide range of tissues, and recent findings indicate a role for this receptor in the control of adipogenesis. Pharmacological and gene-targeting studies have demonstrated a physiological role for PPARs in lipid and lipoprotein metabolism. PPAR controls plasma lipid transport by acting on triglyceride and fatty acid metabolism and by modulating bile acid synthesis and catabolism in the liver. All 3 PPARs regulate macrophage cholesterol homeostasis. By enhancing cholesterol efflux, they stimulate the critical steps of the reverse cholesterol transport pathway. As such, PPARs control plasma levels of cholesterol and triglycerides, which constitute major risk factors for coronary heart disease. Furthermore, PPAR and PPAR regulate the expression of key proteins involved in all stages of atherogenesis, such as monocyte and lymphocyte recruitment to the arterial wall, foam cell formation, vascular inflammation, and thrombosis. Thus, by regulating gene transcription, PPARs modulate the onset and evolution of metabolic disorders predisposing to atherosclerosis and exert direct antiatherogenic actions at the level of the vascular wall.
Key Words: nuclear receptors • HDL • inflammation • cholesterol • atherosclerosis
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