首页> 美国卫生研究院文献>Oncotarget >Ganglioside GM1 contributes to extracellular/intracellular regulation of insulin resistance impairment of insulin signaling and down-stream eNOS activation in human aortic endothelial cells after short- or long-term exposure to TNFα
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Ganglioside GM1 contributes to extracellular/intracellular regulation of insulin resistance impairment of insulin signaling and down-stream eNOS activation in human aortic endothelial cells after short- or long-term exposure to TNFα

机译:神经节苷脂GM1有助于短期或长期接触TNFα的人主动脉内皮细胞中胰岛素抵抗的细胞外/细胞内调节胰岛素信号传导障碍和下游eNOS激活

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摘要

Vascular insulin resistance induced by inflammatory cytokines leads to the initiation and development of vascular diseases. In humans, circulating TNFα levels are increased during aging, suggesting a correlation between vascular insulin resistance and plasma TNFα levels. Currently, the precise molecular mechanisms of vascular insulin resistance mediated by TNFα are not well characterized. We aimed at clarifying whether glycosphingolipids contribute to vascular insulin resistance after inflammatory stimulation. In this study, we examined vascular insulin resistance using human aortic endothelial cells after treatment with different concentrations of TNFα for different time intervals for mimicking in vivo acute or chronic inflammatory situations. We show that ganglioside GM1 levels on cell membranes change depending on time of exposure to TNFα and its concentration and that the GM1 expression is associated with specific extracellular/intracellular regulation of the insulin signaling cascade. Furthermore, we provide evidence that factors such as aging and senescence affect the regulation of insulin resistance. Our data suggest that GM1 is a key player in the induction of vascular insulin resistance after short- or long-term exposure to TNFα and is a good extracellular target for prevention and cure of vascular diseases.
机译:炎性细胞因子诱导的血管胰岛素抵抗导致血管疾病的发生和发展。在人类中,循环中的TNFα水平在衰老过程中会增加,这表明血管胰岛素抵抗与血浆TNFα水平之间存在相关性。目前,由TNFα介导的血管胰岛素抵抗的精确分子机制尚未得到很好的表征。我们旨在阐明在炎性刺激后糖鞘脂是否有助于血管胰岛素抵抗。在这项研究中,我们使用人主动脉内皮细胞在不同时间间隔内用不同浓度的TNFα进行治疗,以模拟体内急性或慢性炎症情况,从而检查了血管胰岛素抵抗。我们显示,细胞膜上神经节苷脂GM1的水平根据暴露于TNFα的时间及其浓度而变化,并且GM1的表达与胰岛素信号级联反应的特定细胞外/细胞内调节有关。此外,我们提供证据表明诸如衰老和衰老等因素会影响胰岛素抵抗的调节。我们的数据表明,GM1是短期或长期接触TNFα后诱导血管胰岛素抵抗的关键因素,并且是预防和治愈血管疾病的良好细胞外靶标。

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