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首页> 外文期刊>FEBS letters. >MiR-146a inhibits oxidized low-density lipoprotein-induced lipid accumulation and inflammatory response via targeting toll-like receptor 4.
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MiR-146a inhibits oxidized low-density lipoprotein-induced lipid accumulation and inflammatory response via targeting toll-like receptor 4.

机译:MiR-146a通过靶向toll样受体4抑制氧化的低密度脂蛋白诱导的脂质蓄积和炎症反应。

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摘要

Atherosclerosis is an inflammatory process due to oxidized low-density lipoprotein (oxLDL) accumulation in macrophages. We investigated the involvement of microRNAs in oxLDL accumulation and inflammatory response in macrophages. The expression of miR-146a decreases under oxLDL stimulation. MiR-146a significantly reduces intracellular LDL cholesterol content and secretion of interleukin 6, interleukin 8, chemokine (C-C motif) ligand 2 and matrix metallopeptidase 9. Toll-like receptor 4 (TLR4) is a relevant target of miR-146a, and miR-146a inhibits the activation of TLR4-dependent intracellular signaling pathways involved in cytoskeleton rearrangement, lipid uptake, and inflammatory cytokine secretion. These results indicate that miR-146a contributes to the regulation of both oxLDL accumulation and inflammatory response by negatively regulating TLR4 and thereby inhibiting the activation of TLR4-dependent signaling pathways. Over-expression of miR-146a may be useful in the prevention and treatment of atherosclerosis.
机译:动脉粥样硬化是由于巨噬细胞中氧化的低密度脂蛋白(oxLDL)积累而引起的炎症过程。我们调查了microRNA在oxLDL积累和巨噬细胞炎症反应中的参与。在oxLDL刺激下,miR-146a的表达降低。 MiR-146a显着降低了细胞内LDL胆固醇含量,并降低了白介素6,白介素8,趋化因子(CC基序)配体2和基质金属肽酶9的分泌。Toll样受体4(TLR4)是miR-146a和miR- 146a抑制与细胞骨架重排,脂质摄取和炎症性细胞因子分泌有关的TLR4依赖性细胞内信号通路的激活。这些结果表明,miR-146a通过负调节TLR4从而抑制TLR4依赖性信号通路的激活,从而有助于oxLDL的积累和炎症反应的调节。 miR-146a的过表达可能有助于预防和治疗动脉粥样硬化。

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