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首页> 外文期刊>Journal of biological inorganic chemistry: JBIC: a publication of the Society of Biological Inorganic Chemistry >Selenium suppresses oxidative-stress-enhanced vascular smooth muscle cell calcification by inhibiting the activation of the PI3K/AKT and ERK signaling pathways and endoplasmic reticulum stress
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Selenium suppresses oxidative-stress-enhanced vascular smooth muscle cell calcification by inhibiting the activation of the PI3K/AKT and ERK signaling pathways and endoplasmic reticulum stress

机译:硒通过抑制PI3K / AKT和ERK信号通路的激活以及内质网应激来抑制氧化应激增强的血管平滑肌细胞钙化

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Vascular calcification is a prominent feature of many diseases, including atherosclerosis, and it has emerged as a powerful predictor of cardiovascular morbidity and mortality. A number of studies have examined the association between selenium and risk of cardiovascular diseases, but little is known about the role of selenium in vascular calcification. To determine the role of selenium in regulating vascular calcification, we assessed the effect of sodium selenite on oxidative-stress-enhanced vascular smooth muscle cell (VSMC) calcification and the underlying mechanism. Oxidative stress induced by xanthine/xanthine oxidase increased apoptosis, as determined by Hoechst 33342 staining and annexin V/propidium iodide staining, and it enhanced osteoblastic differentiation and calcification of VSMCs, on the basis of alkaline phosphatase activity, the expression of Runx2 and type I collagen, and calcium deposition. These effects of oxidative stress were significantly inhibited by selenite. The following processes may explain the inhibitory effects of selenite: (1) selenite significantly suppressed oxidative stress, as evidenced by the decrease of the oxidative status of the cell and lipid peroxidation levels, as well as by the increase of the total protein thiol content and the activity of the antioxidant selenoenzyme glutathione peroxidase; (2) selenite significantly attenuated oxidative-stress-induced activation of the phosphatidylinositol 3-kinase/AKT and extracellular-signal-regulated kinase signaling pathways, resulting in decreased osteoblastic differentiation of VSMCs; (3) selenite significantly inhibited oxidativestress-activated endoplasmic reticulum stress, thereby leading to decreased apoptosis. Our results suggest a potential role of selenium in the prevention of vascular calcification, which may provide more mechanistic insights into the relationship between selenium and cardiovascular diseases.
机译:血管钙化是包括动脉粥样硬化在内的许多疾病的显着特征,它已成为心血管疾病发病率和死亡率的有力预测指标。许多研究已经检查了硒与心血管疾病风险之间的关系,但对硒在血管钙化中的作用知之甚少。为了确定硒在调节血管钙化中的作用,我们评估了亚硒酸钠对氧化应激增强的血管平滑肌细胞(VSMC)钙化的影响及其潜在机制。根据Hoechst 33342染色和膜联蛋白V /碘化丙啶染色,黄嘌呤/黄嘌呤氧化酶诱导的氧化应激增加了细胞凋亡,并在碱性磷酸酶活性,Runx2和I型表达的基础上,增强了VSMC的成骨细胞分化和钙化。胶原蛋白和钙沉积。亚硒酸盐可显着抑制氧化应激的这些作用。以下过程可能解释了亚硒酸盐的抑制作用:(1)亚硒酸盐显着抑制了氧化应激,这通过细胞氧化状态的降低和脂质过氧化水平以及总蛋白硫醇含量和抗氧化剂硒代酶谷胱甘肽过氧化物酶的活性; (2)亚硒酸盐显着减弱了氧化应激诱导的磷脂酰肌醇3-激酶/ AKT的活化和细胞外信号调节的激酶信号传导途径,导致VSMC的成骨细胞分化减少; (3)亚硒酸盐显着抑制氧化应激激活的内质网应激,从而导致细胞凋亡减少。我们的研究结果表明硒在预防血管钙化中的潜在作用,这可能为硒与心血管疾病之间的关系提供更多的机理见解。

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