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首页> 外文期刊>The international journal of biochemistry and cell biology >TNF-alpha induces vascular endothelial cells apoptosis through overexpressing pregnancy induced noncoding RNA in Kawasaki disease model
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TNF-alpha induces vascular endothelial cells apoptosis through overexpressing pregnancy induced noncoding RNA in Kawasaki disease model

机译:TNF-α通过在川崎病模型中过表达妊娠诱导的非编码RNA诱导血管内皮细胞凋亡

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摘要

Kawasaki disease (KD) is an autoimmune disease in which the medium-sized blood vessels throughout the body become inflamed. The increased evidences showed that TNF-alpha was association with vascular inflammation in KD patients. However the detailed mechanism was still unclear. Recent studies indicated abnormal expressed long non-coding RNAs (LncRNAs) involved in many diseases. Thus the purpose of this study is to explore the role of LncRNAs in KD and find out the new target for KD treatment. In this study, firstly we verified the overexpressed TNF-alpha in KD patients, and found TNF-alpha was able to induce HUVECs apoptosis and inhibit HUVECs proliferation. After this we screened out pregnancy induced noncoding RNA (PINC) was significantly overexpression in TNF-alpha treated HUVECs. We also found PINC overexpressed in KD patients. For further study, we designed two siRNA of PINC. After silenced the expression of PINC in HUVECs, we found the Knockdown of PINC enhanced the viability of HUVECs treated with TNF-alpha, and increased the expression of anti-apoptotic and reduced the expression of apoptotic gene. These results suggest PINC involves in the process of TNF-alpha induces vascular endothelial cell apoptosis, it may become a new target for KD treatment. (C) 2016 The Authors. Published by Elsevier Ltd.
机译:川崎病(KD)是一种自身免疫性疾病,其中遍布全身的中型血管发炎。越来越多的证据表明,TNF-α与KD患者的血管炎症有关。但是,具体机制仍不清楚。最近的研究表明,异常表达的长非编码RNA(LncRNA)与许多疾病有关。因此,本研究的目的是探讨LncRNA在KD中的作用,并寻找KD治疗的新靶标。在这项研究中,我们首先验证了KD患者中过表达的TNF-α,发现TNF-α能够诱导HUVEC凋亡并抑制HUVEC增殖。此后,我们筛选出了在TNF-α治疗的HUVEC中妊娠诱导的非编码RNA(PINC)明显过表达。我们还发现PINC在KD患者中过表达。为了进一步研究,我们设计了两个PINC的siRNA。沉默PINC在HUVECs中的表达后,我们发现PINC的敲除增强了TNF-α处理的HUVECs的活力,并增加了抗凋亡蛋白的表达并降低了凋亡基因的表达。这些结果表明PINC参与了TNF-α诱导血管内皮细胞凋亡的过程,可能成为KD治疗的新靶点。 (C)2016作者。由Elsevier Ltd.发布

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