首页> 外文期刊>Molecular and Cellular Biochemistry: An International Journal for Chemical Biology >MicroRNA-221/222 regulate ox-LDL-induced endothelial apoptosis via Ets-1/p21 inhibition
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MicroRNA-221/222 regulate ox-LDL-induced endothelial apoptosis via Ets-1/p21 inhibition

机译:MicroRNA-221 / 222通过抑制Ets-1 / p21调节ox-LDL诱导的内皮细胞凋亡

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摘要

Endothelial cells (ECs) apoptosis induced by oxidized low-density lipoprotein (ox-LDL) is thought to play an essential role in atherosclerosis. MicroRNAs (miRNAs) are a class of short non-coding RNAs, acting as posttranscriptional regulators of protein-coding genes involved in vascular cell biology. MiRNA-221 and miRNA-222 (miR-221/222) are known to be involved in the regulation of endothelial inflammation and angiogenesis. However, the function of miR-221/222 in ox-LDL-induced ECs apoptosis and atherosclerosis is still unknown. Here, we showed that miR-221/222 expression was markedly down-regulated in ox-LDL-induced apoptotic human umbilical cord vein endothelial cells. MiR-221/222 inhibition enhanced apoptosis in ECs, whereas over-expression of miR-221/222 could partly alleviate apoptotic cell death mediated by ox-LDL through suppression of Ets-1 and its downstream target p21. These findings suggest that manipulation of the miR-221/222-Ets-1-p21 pathway may offer a novel strategy for treatment of endothelial apoptosis and atherosclerosis.
机译:氧化低密度脂蛋白(ox-LDL)诱导的内皮细胞(ECs)凋亡被认为在动脉粥样硬化中起重要作用。微小RNA(miRNA)是一类短的非编码RNA,充当参与血管细胞生物学的蛋白质编码基因的转录后调节剂。已知MiRNA-221和miRNA-222(miR-221 / 222)与内皮炎症和血管生成的调控有关。然而,miR-221 / 222在ox-LDL诱导的EC凋亡和动脉粥样硬化中的功能仍然未知。在这里,我们表明在ox-LDL诱导的凋亡的人脐带静脉内皮细胞中,miR-221 / 222的表达明显下调。 MiR-221 / 222的抑制作用增强了EC的凋亡,而miR-221 / 222的过表达可以通过抑制Ets-1及其下游靶点p21来部分缓解由ox-LDL介导的凋亡细胞死亡。这些发现表明,对miR-221 / 222-Ets-1-p21途径的操纵可能为治疗内皮细胞凋亡和动脉粥样硬化提供新的策略。

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