Fas/Fas ligand-mediated death pathway is involved in oxLDL-induced apoptosis in vascular smooth muscle cells

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 基因 平滑肌
作者
Tzong‐Shyuan Lee,Lee‐Young Chau
出处
期刊:American Journal of Physiology-cell Physiology [American Physical Society]
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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