Fas配体
细胞凋亡
程序性细胞死亡
血管平滑肌
细胞生物学
下调和上调
诱导剂
活性氧
半胱氨酸蛋白酶
化学
生物
癌症研究
内分泌学
生物化学
平滑肌
基因
作者
Tzong‐Shyuan Lee,Lee‐Young Chau
出处
期刊:American Journal of Physiology-cell Physiology
[American Physiological Society]
日期:2001-03-01
卷期号:280 (3): C709-C718
被引量:89
标识
DOI:10.1152/ajpcell.2001.280.3.c709
摘要
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, 7β-hydroxycholesterol and 25-hydroxycholesterol, were also effective to induce the expression of death mediators and apoptosis. α-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.
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