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Reconstituted High-Density Lipoprotein Modulates Activation of Human Leukocytes

机译:重构的高密度脂蛋白调节人类白细胞的激活

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摘要

An anti-inflammatory effect of reconstituted High Density Lipoprotein (rHDL) has been demonstrated in atherosclerosis and in sepsis models. An increase of adhesion molecules as well as tissue factor expression on endothelial cells in response to inflammatory or danger signals are attenuated by the treatment with rHDL. Here we show the inhibitory effect of rHDL on the activation of human leukocytes in a whole blood assay as well as on monocyte-derived human dendritic cells (DC). Multiplex analysis of human whole blood showed that phytohaemagglutinin (PHA)-induced secretion of the cytokines IL-1β, IL-1RA, IL-2R, IL-6, IL-7, IL-12(p40), IL-15 and IFN-α was inhibited. Furthermore, an inhibitory effect on the production of the chemokines CCL-2, CCL-4, CCL-5, CXCL-9 and CXCL-10 was observed. Activation of granulocytes and CD14+ monocytes by PHA is inhibited dose-dependently by rHDL shown as decreased up-regulation of ICAM-1 surface expression. In addition, we found a strong inhibitory effect of rHDL on toll-like receptor 2 (TLR2)- and TLR4-mediated maturation of DC. Treatment of DC with rHDL prevented the up-regulation of cell surface molecules CD80, CD83 and CD86 and it inhibited the TLR-driven activation of inflammatory transcription factor NF-κB. These findings suggest that rHDL prevents activation of crucial cellular players of cellular immunity and could therefore be a useful reagent to impede inflammation as well as the link between innate and adaptive immunity.
机译:重组高密度脂蛋白(rHDL)的抗炎作用已在动脉粥样硬化和败血症模型中得到证实。通过rHDL的治疗减弱了对炎症或危险信号响应的内皮细胞上粘附分子以及组织因子表达的增加。在这里,我们显示了rHDL在全血测定中以及对单核细胞衍生的人树突状细胞(DC)的激活对人类白细胞的抑制作用。人类全血的多重分析表明,植物血凝素(PHA)诱导了细胞因子IL-1β,IL-1RA,IL-2R,IL-6,IL-7,IL-12(p40),IL-15和IFN的分泌-α被抑制。此外,观察到对趋化因子CCL-2,CCL-4,CCL-5,CXCL-9和CXCL-10产生的抑制作用。 RHDL剂量依赖性地抑制PHA激活粒细胞和CD14 + 单核细胞,表现为ICAM-1表面表达的上调。此外,我们发现rHDL对通行费样受体2(TLR2)和TLR4介导的DC成熟具有强烈的抑制作用。用rHDL处理DC可防止细胞表面分子CD80,CD83和CD86的上调,并抑制TLR驱动的炎症转录因子NF-κB的激活。这些发现表明,rHDL阻止了细胞免疫的关键细胞参与者的活化,因此可能是阻止炎症以及先天免疫和适应性免疫之间联系的有用试剂。

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