Induction of antioxidant stress proteins in vascular endothelial and smooth muscle cells: Protective action of vitamin C against atherogenic lipoproteins

• Published in: Free radical research 1999-01, Vol.31 (4), p.309-318
• Main Authors: Siow, Richard C.M., Sato, Hideyo, Leake, David S., Ishii, Tetsuro, Bannai, Shiro, Mann, Giovanni E.
• Format: Article
• Language: English
• Subjects: Animals; Antioxidant stress proteins; Antioxidants - metabolism; Antioxidants - pharmacology; Antioxidants - therapeutic use; apoptosis; Arteriosclerosis - etiology; Arteriosclerosis - metabolism; Arteriosclerosis - pathology; Arteriosclerosis - prevention & control; Ascorbic Acid - metabolism; Ascorbic Acid - pharmacology; Ascorbic Acid - therapeutic use; Endothelium, Vascular - metabolism; Endothelium, Vascular - pathology; Free Radicals; heme oxygenase-1; Humans; Lipid Peroxidation; low density lipoproteins; MSP23; Muscle, Smooth, Vascular - metabolism; Muscle, Smooth, Vascular - pathology; Reactive Oxygen Species - metabolism; vascular endothelial cells; vascular smooth muscle; vitamin C
• ISSN: 1071-5762; 1029-2470
• DOI: 10.1080/10715769900300871

Elevated levels of lipid peroxidation and increased formation of reactive oxygen species within the vascular wall in atherosclerosis can overwhelm cellular antioxidant defence mechanisms. Accumulating evidence implicates oxidatively modified low density lipoproteins (LDL) in vascular dysfunction in atherosclerosis and oxidized LDL have been localized with in atherosclerotic lesions. We here report that human oxidatively modified LDL induce expression of 'antioxidant-like' stress proteins in vascular cells, involving increases in the activity of l-cystine transport, glutathione synthesis, heme oxygenase-1 and the murine stress protein MSP23. Moreover, treatment of human arterial smooth muscle cells with the dietary antioxidant vitamin C markedly attenuates adaptive increases in endogenous antioxidant gene expression and affords protection against smooth muscle cell apoptosis induced by moderately oxidized LDL. As vascular cell death is a key feature of atherosclerotic lesions and may contribute to the plaque 'necrotic' core, cap rupture and thrombosis, our findings suggest that the cytoprotective actions of vitamin C could limit plaque instability in advanced atherosclerosis.