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Division of Cardiovascular Research, Institute of Biomedical Sciences, Academia Sinica, Taipei 11529, Taiwan, Republic of China
Oxidized
low-density lipoprotein (oxLDL) is a potent inducer of
apoptosis for vascular cells. In the present study, we
demonstrate that the expression of death mediators, including p53, Fas,
and Fas ligand (FasL) was substantially upregulated by oxLDL in
cultured vascular smooth muscle cells (SMCs). The induction of these
death mediators was time dependent and was accompanied by an increase in apoptotic death of SMCs following oxLDL treatment. Two
oxysterols, 7
-hydroxycholesterol and 25-hydroxycholesterol, were
also effective to induce the expression of death mediators and
apoptosis.
-Tocopherol and deferoxamine significantly
attenuated the induction of death mediators and cell death induced by
oxLDL and oxysterols, suggesting that reactive oxygen species are
involved in triggering the apoptotic event. Incubation of cells
with FasL-neutralizing antibody inhibited the oxLDL-induced cell death
up to 50%. Furthermore, caspase 8 and caspase 3 activities were
induced time dependently in SMCs following oxLDL treatment.
Collectively, these data suggest that the Fas/FasL death pathway is
activated and responsible for, at least in part, the apoptotic
death in vascular SMCs upon exposure to oxLDL.
atherosclerosis; oxysterols; p53; caspase; oxidized low-density lipoprotein
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