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High density lipoprotein mediates anti-inflammatory transcriptional reprogramming of macrophages via the transcriptional repressor ATF3

机译:高密度脂蛋白通过转录阻遏物ATF3介导巨噬细胞的抗炎转录重编程

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摘要

High Density Lipoprotein (HDL) mediates reverse cholesterol transport and it is known to be protective against atherosclerosis. In addition, HDL has potent anti-inflammatory properties that may be critical for protection against other inflammatory diseases. The molecular mechanisms of how HDL can modulate inflammation, particularly in immune cells such as macrophages, remain poorly understood. Here we identify the transcriptional repressor ATF3, as an HDL-inducible target gene in macrophages that down-regulates the expression of Toll-like receptor (TLR)-induced pro-inflammatory cytokines. The protective effects of HDL against TLR-induced inflammation were fully dependent on ATF3 in vitro and in vivo. Our findings may explain the broad anti-inflammatory and metabolic actions of HDL and provide the basis for predicting the success of novel HDL-based therapies.
机译:高密度脂蛋白(HDL)介导胆固醇逆向转运,并且已知对动脉粥样硬化具有保护作用。此外,HDL具有强效的抗炎特性,对于保护抵抗其他炎性疾病可能至关重要。 HDL如何调节炎症的分子机制,尤其是在诸如巨噬细胞之类的免疫细胞中,尚不清楚。在这里,我们确定转录抑制因子ATF3是巨噬细胞中的HDL诱导靶基因,它可以下调Toll样受体(TLR)诱导的促炎细胞因子的表达。 HDL对TLR诱导的炎症的保护作用在体外和体内完全取决于ATF3。我们的发现可能解释了HDL的广泛抗炎和代谢作用,并为预测基于HDL的新型疗法的成功提供了基础。

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