首页> 美国卫生研究院文献>Aging (Albany NY) >Downregulation of interleukin-6 and C-reactive protein underlies a novel inhibitory role of microRNA-136-5p in acute lower extremity deep vein thrombosis
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Downregulation of interleukin-6 and C-reactive protein underlies a novel inhibitory role of microRNA-136-5p in acute lower extremity deep vein thrombosis

机译:白细胞介素-6和C反应蛋白的下调是MicroRNA-136-5P在急性下肢深静脉血栓形成中的新抑制作用

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摘要

Deep vein thrombosis (DVT) comprises a critical and common health condition with high incidence, mortality, and long-term adverse sequelae. Several differentially expressed microRNAs (miRNAs) have emerged as promising prognostic markers in DVT. The present study intended to explore the functional relevance of miR-136-5p in acute lower extremity DVT (LEDVT). Rat models of acute LEDVT were established and miR-136-5p expression was altered by agomir or antagomir to assess its effects. In addition, in vitro gain- and loss-experiments, prior to exposure to CoCl2, were performed to investigate effects of miR-136-5p on human umbilical vein endothelial cell (HUVEC) apoptosis and levels of interleukin-6 (IL-6) and C-reactive protein (CRP). miR-136-5p was downregulated, whereas IL-6 and CRP were elevated in acute LEDVT patients. Notably, miR-136-5p was confirmed to target both IL-6 and CRP. Overexpression of miR-136-5p led to reduced length, weight, and ratio of weight to length of the venous thrombus. Furthermore, overexpressed miR-136-5p downregulated the expression of IL-6 and CRP, consequently inhibiting HUVEC apoptosis. Conjointly, our data indicate that the overexpression of miR-136-5p has the potential to bind to the 3’-UTR in the mRNAs for IL-6 and CRP and mitigate acute LEDVT, which provides a basis for new therapeutic targets in acute LEDVT treatment.
机译:深静脉血栓形成(DVT)包含具有高发病率,死亡率和长期不良后遗症的关键和常见的健康状况。几种差异表达的MicroRNA(miRNA)被出现为DVT中有希望的预后标志物。本研究旨在探讨急性下肢DVT(LEDVT)中miR-136-5p的功能相关性。建立了大鼠急性铅型的模型,并通过Agomir或Antagomir改变MiR-136-5P表达,以评估其效果。此外,在暴露于COCl2之前的体外增益和丧失实验是为了研究MIR-136-5P对人脐静脉内皮细胞(HUVEC)凋亡和白细胞介素-6(IL-6)的影响和C反应蛋白(CRP)。下调miR-136-5p,而IL-6和CRP在急性铅患者中升高。值得注意的是,MiR-136-5P被证实靶向IL-6和CRP。 miR-136-5p的过度表达导致长度,重量和重量的重量与静脉血栓的长度。此外,过表达MiR-136-5P下调了IL-6和CRP的表达,从而抑制Huvec凋亡。联合,我们的数据表明miR-136-5p的过表达具有潜在的IL-6和CRP中的3'-UTR中的3'-UTR,并减轻急性LEDVT,为急性铅液中的新治疗靶标提供依据治疗。

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