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人源巨噬细胞对 L. (Viannia) panamensis 的反应:微阵列证据表明存在早期炎症反应。

Human macrophage response to L. (Viannia) panamensis: microarray evidence for an early inflammatory response.

机构信息

Centro Internacional de Entrenamiento e Investigaciones Médicas (CIDEIM), Cali, Colombia.

出版信息

PLoS Negl Trop Dis. 2012;6(10):e1866. doi: 10.1371/journal.pntd.0001866. Epub 2012 Oct 25.

Abstract

BACKGROUND

Previous findings indicate that susceptibility to Leishmania (Viannia) panamensis infection of monocyte-derived macrophages from patients and asymptomatically infected individuals were associated with the adaptive immune response and clinical outcome.

METHODOLOGY/PRINCIPAL FINDINGS: To understand the basis for this difference we examined differential gene expression of human monocyte-derived macrophages following exposure to L. (V.) panamensis. Gene activation profiles were determined using macrophages from healthy volunteers cultured with or without stationary phase promastigotes of L. (V.) panamensis. Significant changes in expression (>1.5-fold change; p<0.05; up- or down-regulated) were identified at 0.5, 4 and 24 hours. mRNA abundance profiles varied over time, with the highest level of activation occurring at earlier time points (0.5 and 4 hrs). In contrast to observations for other Leishmania species, most significantly changed mRNAs were up- rather than down-regulated, especially at early time points. Up-regulated transcripts over the first 24 hours belonged to pathways involving eicosanoid metabolism, oxidative stress, activation of PKC through G protein coupled receptors, or mechanism of gene regulation by peroxisome proliferators via PPARα. Additionally, a marked activation of Toll-receptor mediated pathways was observed. Comparison with published microarray data from macrophages infected with L. (Leishmania) chagasi indicate differences in the regulation of genes involved in signaling, motility and the immune response.

CONCLUSIONS

Results show that the early (0.5 to 24 hours) human monocyte-derived macrophage response to L. (Viannia) panamensis is not quiescent, in contrast to published reports examining later response times (48-96 hours). Early macrophage responses are important for the developing cellular response at the site of infection. The kinetics and the mRNA abundance profiles induced by L. (Viannia) panamensis illustrate the dynamics of these interactions and the distinct biologic responses to different Leishmania species from the outset of infection within their primary host cell.

摘要

背景

先前的研究结果表明,来自患者和无症状感染者的单核细胞来源的巨噬细胞对莱什曼原虫(Viannia)panamensis 感染的易感性与适应性免疫反应和临床结果有关。

方法/主要发现:为了了解这种差异的基础,我们研究了人类单核细胞来源的巨噬细胞在暴露于 L.(V.)panamensis 后的差异基因表达。使用来自健康志愿者的巨噬细胞,在有无 L.(V.)panamensis 静止期前体的情况下培养,确定基因激活谱。使用 L.(V.)panamensis 静止期前体培养巨噬细胞,发现 0.5、4 和 24 小时后表达(>1.5 倍变化;p<0.05;上调或下调)显著变化。mRNA 丰度谱随时间变化,激活水平最高发生在较早的时间点(0.5 和 4 小时)。与其他莱什曼物种的观察结果相反,大多数变化最显著的 mRNAs 上调而非下调,尤其是在早期时间点。在最初 24 小时内上调的转录物属于涉及类二十烷酸代谢、氧化应激、通过 G 蛋白偶联受体激活 PKC 或过氧化物酶体增殖物激活受体α通过 PPARα调节基因表达的机制的途径。此外,还观察到 Toll 受体介导途径的明显激活。与巨噬细胞感染 L.(Leishmania)chagasi 的已发表微阵列数据进行比较,表明参与信号转导、运动和免疫反应的基因调控存在差异。

结论

结果表明,与研究较晚反应时间(48-96 小时)的已发表报告相反,人类单核细胞来源的巨噬细胞对 L.(Viannia)panamensis 的早期(0.5 至 24 小时)反应不是静止的。早期巨噬细胞反应对于感染部位发育中的细胞反应很重要。L.(Viannia)panamensis 诱导的动力学和 mRNA 丰度谱说明了这些相互作用的动态以及从主要宿主细胞感染开始,不同莱什曼物种的独特生物学反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/277c/3493378/7bc1dcbe68f4/pntd.0001866.g001.jpg

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