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The cellular and immunological consequences of LLO mediated vacuolar escape.

机译:LLO介导的液泡逃逸的细胞和免疫学后果。

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Listeria monocytogenes is a Gram-positive facultative intracellular pathogen capable of causing severe food born illness. Escape from the phagosome is essential for the intracellular life cycle of L. monocytogenes and has tremendous consequences on many biological processes including protective immunity and autophagy.;Wild-type L. monocytogenes express the gene hly that results in the production of the cholesterol dependent cytolysin listeriolysin O (LLO). Expression of LLO is required for phagosomal escape and for the induction of a cell-mediated immune response to L. monocytogenes . A mutant of L. monocytogenes that does not express LLO is avirulent, remains trapped in the phagosome, and is unable induce cell-mediated immunity. The reason that L. monocytogenes mutants, lacking LLO, do not induce a cell-mediated immune response is not understood.;Using a mixed inoculum of cytosolic and phagosome-trapped L. monocytogenes we found that when L. monocytogenes was confined to the vacuole, it suppressed the immunizing capability of L. monocytogenes in the cytosol. Further, as we increased the concentration of the bacteria trapped in the phagosome with an inoculum containing an immunizing dose of cytosolic L. monocytogenes, a concomitant decrease in the expression of pro-inflammatory cytokines and L. monocytogenes specific T cells was observed. Additionally, immunosuppressive cytokines, including IL10, were made in response to bacteria trapped in the phagosome, and blockage of the IL10R restored the immunizing capability of cytosolic L. monocytogenes even in the presence of phagosome-trapped bacteria.;L. monocytogenes escape from the phagosome also induced autophagy. Autophagy is cellular bulk degradation pathway used to degrade long-lived proteins and organelles. We found L. monocytogenes mutants lacking LLO did not induce autophagy, whereas wild-type and other mutants induced relatively equal amounts of autophagy early in an infection of bone marrow derived macrophages. Bacillus subtilis expressing LLO also induced autophagy, indicating that the induction was not specific to L. monocytogenes. Lastly, we found that liposomes containing LLO were sufficient to induce autophagy in the absence of infection. Thus, LLO was necessary and sufficient to induce autophagy in an L. monocytogenes infection.;In summary, we found that LLO expression by L. monocytogenes was required for both the proper induction of the cell-mediated immune response to L. monocytogenes and was also required for the induction of autophagy in response to infection with L. monocytogenes .
机译:单核细胞增生李斯特菌是一种革兰氏阳性兼性细胞内病原体,能够引起严重的食源性疾病。逃离吞噬体对于单核细胞增生李斯特菌的细胞内生命周期至关重要,并且对许多生物学过程(包括保护性免疫和自噬)都具有重大影响。野生型单核细胞增生李斯特表达可导致胆固醇依赖性溶血素产生的基因hly李斯特菌溶血素O(LLO)。 LLO的表达是吞噬体逃逸和诱导对单核细胞增生李斯特氏菌的细胞介导的免疫反应所必需的。不表达LLO的单核细胞增生李斯特氏菌的突变体是无毒的,仍被捕获在吞噬体中,并且不能诱导细胞介导的免疫。不了解缺乏LLO的单核细胞增生李斯特氏菌突变体不能诱导细胞介导的免疫反应的原因尚不清楚;使用细胞溶质和吞噬体捕获的单核细胞增生李斯特菌的混合接种物,我们发现当单核细胞增生李斯特菌局限于空泡时,它抑制了细胞溶质中单核细胞增生李斯特菌的免疫能力。此外,随着我​​们使用含有免疫剂量胞质单核细胞增生李斯特菌的接种物提高吞噬体中捕获的细菌浓度,观察到促炎性细胞因子和单核细胞增生李斯特氏菌特异性T细胞的表达随之降低。另外,响应被困在吞噬体中的细菌,产生了包括IL10在内的免疫抑制细胞因子,并且IL10R的阻断甚至在存在被吞噬体捕获的细菌的情况下也恢复了胞浆单核细胞增生李斯特菌的免疫能力。单核细胞增生因子也从吞噬体逃逸,并诱导自噬。自噬是用于降解长寿蛋白和细胞器的细胞大量降解途径。我们发现缺乏LLO的单核细胞增生李斯特氏菌突变体不会诱导自噬,而在感染骨髓衍生的巨噬细胞的早期,野生型和其他突变体会诱导相对等量的自噬。表达LLO的枯草芽孢杆菌也诱导自噬,表明该诱导对单核细胞增生李斯特氏菌不是特异性的。最后,我们发现含有LLO的脂质体足以在没有感染的情况下诱导自噬。因此,LLO在单核细胞增生李斯特氏菌感染中诱导自噬是必要和充分的。总而言之,我们发现单核细胞增生李斯特氏菌表达LLO是正确诱导细胞介导的针对单核细胞增生李斯特氏菌的免疫反应所必需的。也需要诱导自噬细胞感染单核细胞增生李斯特菌。

著录项

  • 作者单位

    University of California, Berkeley.;

  • 授予单位 University of California, Berkeley.;
  • 学科 Biology Cell.;Biology Microbiology.
  • 学位 Ph.D.
  • 年度 2009
  • 页码 100 p.
  • 总页数 100
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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