肝片形吸虫ESPs可以模糊地激活或阻断人单核细胞系中的多个toll样受体。

Annals of clinical pathology Pub Date : 2017-01-01 Epub Date: 2017-03-31
Olgary Figueroa-Santiago, Ana M Espino
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引用次数: 0

摘要

肝片形吸虫是一种寄生蠕虫,在其哺乳动物宿主体内诱导Th2/Treg反应。一些报道表明,在先天免疫的早期阶段,ESPs通过延迟树突状细胞和巨噬细胞的激活来实现这些极化免疫反应,这一过程是由TLR4介导的。本研究旨在探讨除TLR4之外的TLRs是否也能被肝芽胞杆菌esp靶向。为了实现这一目标,我们利用THP1-Blue CD14细胞对筛选系统进行了优化。首先用离子交换色谱法(IEC)根据其分子量和净电荷对电晶体进行分离。结果表明肝梭菌esp主要是组织蛋白酶、丝氨酸蛋白酶和内啡肽,能够激活TLR2、TLR4、TLR8,也可能激活TLR5和TLR6。而脂肪酸结合蛋白则强烈抑制各种tlr配体诱导的刺激。需要进一步的研究来了解在活动性感染的背景下,相同蛋白质混合物分子的这些明显的矛盾作用是如何相互补充的,从而导致了肝梭菌感染特征的极化th2免疫反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

<i>Fasciola hepatica</i> ESPs Could Indistinctly Activate or Block Multiple Toll-Like Receptors in a Human Monocyte Cell Line.

<i>Fasciola hepatica</i> ESPs Could Indistinctly Activate or Block Multiple Toll-Like Receptors in a Human Monocyte Cell Line.

<i>Fasciola hepatica</i> ESPs Could Indistinctly Activate or Block Multiple Toll-Like Receptors in a Human Monocyte Cell Line.

Fasciola hepatica ESPs Could Indistinctly Activate or Block Multiple Toll-Like Receptors in a Human Monocyte Cell Line.

Fasciola hepatica is a parasitic helminth that induces Th2/Treg responses in its mammalian host. Some reports have suggested that ESPs achieve these polarized immune responses by delaying the activation of dendritic cells and macrophages during the early stages of innate immunity, a process that is mediated by TLR4. The present study aimed to investigate whether TLRs other than TLR4 could also be targeted by F. hepatica ESPs. To achieve this aim a screening system was optimized using THP1-Blue CD14 cells. ESPs were first separated based on their molecular weight and according their net charge by ion exchange chromatography (IEC). Results demonstrated that F. hepatica ESPs mainly cathepsin, serpin and endopin are capable of activating TLR2, TLR4, TLR8 and likely also TLR5 and TLR6. In contrast, fatty acid binding protein strongly suppressed the stimulation induced by various TLR-ligands. Further studies are needed to understand how these apparent contradictory effects of molecules of the same protein mix complement each other in the context of an active infection resulting in the polarized Th2-immune response that characterize F. hepatica infections.

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