Different patterns of IL-1β secretion, adhesion molecule expression and apoptosis induction in human endothelial cells treated with 7α-, 7β-hydroxycholesterol, or 7-ketocholesterol

• Published in: FEBS letters 1998-12, Vol.440 (3), p.434-439
• Main Authors: Lemaire, Stéphanie, Lizard, Gérard, Monier, Serge, Miguet, Carole, Gueldry, Serge, Volot, Fabienne, Gambert, Philippe, Néel, Dominique
• Format: Article
• Language: English
• Subjects: Adhesion molecule; Apoptosis; Human endothelial cell; Interleukin-1β; Oxysterol; Tumor necrosis factor-α
• ISSN: 0014-5793; 1873-3468
• DOI: 10.1016/S0014-5793(98)01496-3

Among oxysterols oxidized at C7 (7α-, 7β-hydroxycholesterol, and 7-ketocholesterol), 7β-hydroxycholesterol and 7-ketocholesterol involved in the cytotoxicity of oxidized low density lipoproteins (LDL) are potent inducers of apoptosis. Here, we asked whether all oxysterols oxidized at C7 were able to trigger apoptosis, to stimulate interleukin (IL)-1β and/or tumor necrosis factor (TNF)-α secretion, and to enhance adhesion molecule expression (intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), and E-selectin) on human umbilical venous endothelial cells (HUVECs). Only 7β-hydroxycholesterol and 7-ketocholesterol were potent inducers of apoptosis and of IL-1β secretion. TNF-α secretion was never detected. Depending on the oxysterol considered, various levels of ICAM-1, VCAM-1 and E-selectin expression were observed. So, oxysterols oxidized at C7 differently injure and activate HUVECs, and the α- or β-hydroxyl radical position plays a key role in apoptosis and IL-1β secretion.