首页> 外文期刊>Toxicon: An International Journal Devoted to the Exchange of Knowledge on the Poisons Derived from Animals, Plants and Microorganisms >Divergent Pseudomonas exotoxin A sensitivity in normal and transformed liver cells is correlated with low-density lipoprotein receptor-related protein expression
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Divergent Pseudomonas exotoxin A sensitivity in normal and transformed liver cells is correlated with low-density lipoprotein receptor-related protein expression

机译:正常和转化肝细胞中的假单胞菌外毒素A敏感性与低密度脂蛋白受体相关蛋白表达相关

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Pseudomonas exotoxin A (PEA) is an extracellular virulence factor produced by the opportunistic human pathogen Pseudomonas aerguinosa. PEA intoxification begins when PEA binds to the low-density lipoprotein receptor-related protein (LRP). The liver is the primary target of systemic PEA, due largely to the high levels of functional LRP expressed by liver cells. Using a H-3-leucine incorporation assay to measure inhibition of protein synthesis we have demonstrated that normal (BNL CL.2) and transformed (BNL. 1ME A7R.1) liver cells exhibit divergent PEA sensitivity; with BNL 1ME A7R.1 cells demonstrating greater PEA sensitivity than their non-transformed counterparts. The receptor-associated protein, a LRP antagonist, decreased PEA toxicity in BNL 1ME A7R.1 cells, confirming the importance of the LRP in PEA intoxification in this cell type. Increased PEA sensitivity in BNL 1ME A7R.1 cells was associated with increased functional cell surface LRP expression, as measured by alpha (2)-macroglobulin binding and internalization studies, and increased LRP mRNA levels, as determined by Northern blot analysis. Interestingly, BNL CL.2 cells were more sensitive than BNL 1ME A7R.1 cells to conjugate and mutant PEA toxins that do not utilize the LRP for cellular entry. These data demonstrate that increased LRP expression is an important mechanism by which PEA sensitivity is increased in BNL 1ME A7R.1 transformed liver cells. (C) 2001 Elsevier Science Ltd. All rights reserved. [References: 32]
机译:假单胞菌外毒素A(PEA)是由机会性人类病原体铜绿假单胞菌产生的细胞外毒力因子。当PEA结合到低密度脂蛋白受体相关蛋白(LRP)时,PEA毒化开始。肝脏是全身性PEA的主要靶标,这在很大程度上归因于肝细胞表达的高水平的功能性LRP。使用H-3-亮氨酸掺入法来测量蛋白质合成的抑制作用,我们已经证明正常(BNL CL.2)和转化(BNL。1ME A7R.1)肝细胞表现出不同的PEA敏感性。 BNL 1ME A7R.1细胞的PEA敏感性要高于非转化细胞。受体相关蛋白,一种LRP拮抗剂,降低了BNL 1ME A7R.1细胞的PEA毒性,证实了LRP在这种细胞类型的PEA毒化中的重要性。 BNL 1ME A7R.1细胞中PEA敏感性的增加与功能细胞表面LRP表达的增加有关,如通过alpha(2)-巨球蛋白结合和内化研究所测量的,以及LRP mRNA水平的增加,如Northern blot分析所确定的。有趣的是,对于不利用LRP进入细胞的缀合和突变PEA毒素,BNL CL.2细胞比BNL 1ME A7R.1细胞更敏感。这些数据表明,LRP表达的增加是BNL 1ME A7R.1转化肝细胞中PEA敏感性增加的重要机制。 (C)2001 Elsevier ScienceLtd。保留所有权利。 [参考:32]

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