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Damage and activation of endothelial cells during in vitro hypoxia

机译:体外缺氧过程中内皮细胞的损伤和活化

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摘要

We studied the effect of hypoxia on activation and stimulation of apoptosis in cultured endothelial cells. The effect of hypoxia was compared to that of apoptosis-inducing agents (tumor necrosis factor and bacterial lipopolysaccharide). Incubation of endothelial cells for 24 h under hypoxic conditions (2% O 2, 5% CO 2, and 93% N 2) increased secretion of von Willebrand factor, but had no effect on the expression of cell adhesion molecule ICAM-1. Tumor necrosis factor and lipopolysaccharide did not stimulate secretion of von Willebrand factor, but significantly increased the expression of ICAM-1. These data attest to significant differences in the mechanisms of endothelium activation under hypoxic conditions and during treatment with tumor necrosis factor or lipopolysaccharide. Hypoxia stimulated apoptosis in endothelial cells, which was seen from the increase in the number of annexin V-binding cells and activation of caspase-3. Similar changes were revealed in the presence of tumor necrosis factor and lipopolysaccharide. Hence, damage to endothelial cells caused by hypoxia and these compounds is mediated by similar mechanisms.
机译:我们研究了缺氧对培养的内皮细胞激活和凋亡的影响。将缺氧的作用与凋亡诱导剂(肿瘤坏死因子和细菌脂多糖)的作用进行了比较。在缺氧条件下(2%O 2、5%CO 2和93%N 2)孵育内皮细胞24小时可增加von Willebrand因子的分泌,但对细胞粘附分子ICAM-1的表达没有影响。肿瘤坏死因子和脂多糖不刺激血管性假血友病因子的分泌,但显着增加了ICAM-1的表达。这些数据证明在低氧条件下以及在用肿瘤坏死因子或脂多糖治疗期间内皮活化的机制存在显着差异。低氧刺激内皮细胞的凋亡,这是通过膜联蛋白V结合细胞数量的增加和caspase-3的激活而看到的。在存在肿瘤坏死因子和脂多糖的情况下揭示了类似的变化。因此,由缺氧和这些化合物引起的对内皮细胞的损害是由相似的机制介导的。

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