Department of Cardiology, Rui Jin Hospital, Jiaotong University School of Medicine, Shanghai 200025, People's Republic of China.
FEBS Lett. 2011 Mar 23;585(6):854-60. doi: 10.1016/j.febslet.2011.02.009. Epub 2011 Feb 15.
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.
动脉粥样硬化是一种炎症过程,由于巨噬细胞中氧化的低密度脂蛋白(oxLDL)的积累。我们研究了 microRNAs 在巨噬细胞中 oxLDL 积累和炎症反应中的作用。在 oxLDL 刺激下,miR-146a 的表达减少。miR-146a 显著降低细胞内 LDL 胆固醇含量和白细胞介素 6、白细胞介素 8、趋化因子(C-C 基序)配体 2 和基质金属蛋白酶 9 的分泌。Toll 样受体 4(TLR4)是 miR-146a 的一个相关靶标,miR-146a 抑制参与细胞骨架重排、脂质摄取和炎症细胞因子分泌的 TLR4 依赖性细胞内信号通路的激活。这些结果表明,miR-146a 通过负调控 TLR4 参与 oxLDL 积累和炎症反应的调节,从而抑制 TLR4 依赖性信号通路的激活。miR-146a 的过表达可能有助于动脉粥样硬化的预防和治疗。