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首页> 外文期刊>Infection and immunity >Enhanced Macrophage Resistance toPseudomonas Exotoxin A Is Correlated with Decreased Expression of the Low-Density Lipoprotein Receptor-Related Protein
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Enhanced Macrophage Resistance toPseudomonas Exotoxin A Is Correlated with Decreased Expression of the Low-Density Lipoprotein Receptor-Related Protein

机译:对假单胞菌外毒素A增强的巨噬细胞抵抗力与低密度脂蛋白受体相关蛋白的表达降低相关。

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Cellular intoxification by exotoxin A of Pseudomonas aeruginosa (PEA) begins when PEA binds to its cellular receptor, the low-density lipoprotein receptor-related protein (LRP). This receptor is particularly abundant on macrophages. We hypothesize here that inducible changes in cellular expression levels of the LRP represent an important mechanism by which macrophage susceptibility to PEA is regulated by the host. We have examined the effect of lipopolysaccharide (LPS) on LRP expression and PEA sensitivity in the macrophage-like cell line HS-P. Using a [3H]leucine incorporation assay to measure inhibition of protein synthesis, we have demonstrated that HS-P macrophages are highly sensitive to PEA and that PEA toxicity is decreased by the LRP antagonist receptor-associated protein. LPS pretreatment decreases HS-P PEA sensitivity in a time- and dose-dependent manner. The dose of toxin required to inhibit protein synthesis by 50% increased from 11.3 ± 1.2 ng/ml in untreated cells to 25.7 ± 2.0 ng/ml in cells treated with LPS. In pulse experiments, involving brief exposure to saturating concentrations of PEA, [3H]leucine incorporation was more than threefold higher in cells pretreated with LPS than in untreated macrophages. These changes in HS-P PEA sensitivity following LPS treatment were consistently associated with a fivefold decrease in HS-P LRP mRNA expression as measured by Northern blot analysis and a three-and-a-half-fold decrease in HS-P LRP-specific ligand internalization as determined by activated α2-macroglobulin internalization studies. These data demonstrate for the first time that modulation of LRP levels by extracellular signaling molecules can alter cellular PEA sensitivity.
机译:当铜绿假单胞菌(PEA)与其细胞受体(低密度脂蛋白受体相关蛋白(LRP))结合时,就开始受到铜绿假单胞菌(PEA)外毒素A的细胞毒作用。该受体在巨噬细胞上特别丰富。我们在这里假设,LRP的细胞表达水平的诱导性变化代表一种重要的机制,通过该机制宿主可以调节巨噬细胞对PEA的敏感性。我们已经检查了脂多糖(LPS)对巨噬细胞样细胞系HS-P中LRP表达和PEA敏感性的影响。使用[ 3 H]亮氨酸掺入法来测量蛋白质合成的抑制作用,我们已经证明HS-P巨噬细胞对PEA高度敏感,并且LRP拮抗剂受体相关蛋白可降低PEA毒性。 LPS预处理以时间和剂量依赖性方式降低HS-P PEA敏感性。抑制蛋白质合成50%所需的毒素剂量从未经处理的细胞中的11.3±1.2 ng / ml增加到LPS处理的细胞中的25.7±2.0 ng / ml。在脉冲实验中,涉及短暂暴露于饱和浓度的PEA,在用LPS预处理的细胞中,[ 3 H]亮氨酸的掺入比未处理的巨噬细胞高三倍以上。 LPS治疗后,HS-P PEA敏感性的这些变化与通过Northern blot分析测得的HS-P LRP mRNA表达下降了五倍以及HS-P LRP特异性下降了三倍半有关。活化的α 2 -巨球蛋白内部化研究确定了配体的内部化。这些数据首次证明了细胞外信号分子对LRP水平的调节可以改变细胞PEA的敏感性。

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