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蜱唾液对 TLR-2 配体和阿弗西氏伯氏疏螺旋体激活的树突状细胞信号通路的影响。

Effect of tick saliva on signalling pathways activated by TLR-2 ligand and Borrelia afzelii in dendritic cells.

机构信息

Institute of Parasitology, Biology Centre of the Academy of Sciences of Czech Republic, Ceske Budejovice, Czech Republic.

出版信息

Parasite Immunol. 2012 Aug-Sep;34(8-9):421-9. doi: 10.1111/j.1365-3024.2012.01375.x.

Abstract

Dendritic cells are a sentinel in defending against pathogens and tick saliva facilitates transmission of tick-borne pathogens by modulating the host immune response. The maturation of dendritic cells is inhibited by tick saliva. To elucidate the mechanism of this inhibition, we tested the impact of Ixodes ricinus tick saliva on signalling pathways activated by Toll-like receptor (TLR-2) ligand and Borrelia afzelii in spleen dendritic cells. The activation of nuclear factor-κB (NF-κB) p65 and phosphatidylinositol-3 kinase (PI3K)/Akt pathways was decreased by tick saliva upon both TLR-2 and Borrelia stimulation. Among the mitogen-activated protein kinases (MAPK), the activation of extracellular matrix-regulated kinase (Erk1/2) was suppressed by tick saliva, but not p38. In response to spirochaetes, the amount of TNF-α decreased in the presence of tick saliva which was mediated by selective suppression of Erk1/2, NF-κB and Akt as tick saliva mimicked the effect of their specific inhibitors, UO126, IKK-IV and LY294002, respectively. Saliva-induced enhancement of IL-10 was not observed in the presence of specific inhibitor of Protein Kinase A (PKA), H-89, suggesting the involvement of PKA pathway in IL-10 production. Our cumulative data show that tick saliva interferes with several signalling pathways, thus modulating the immune functions of dendritic cells.

摘要

树突状细胞是抵御病原体的哨兵,蜱唾液通过调节宿主免疫反应促进蜱传病原体的传播。蜱唾液抑制树突状细胞的成熟。为了阐明这种抑制的机制,我们测试了伊氏革蜱唾液对 TLR-2 配体和伯氏疏螺旋体激活的脾树突状细胞中信号通路的影响。TLR-2 和伯氏疏螺旋体刺激时,蜱唾液均降低了核因子-κB(NF-κB)p65 和磷脂酰肌醇-3 激酶(PI3K)/Akt 通路的激活。在丝裂原激活的蛋白激酶(MAPK)中,蜱唾液抑制细胞外基质调节激酶(Erk1/2)的激活,但不抑制 p38。在对螺旋体的反应中,TNF-α 的量在蜱唾液存在的情况下减少,这是通过选择性抑制 Erk1/2、NF-κB 和 Akt 介导的,蜱唾液分别模拟了它们的特异性抑制剂 UO126、IKK-IV 和 LY294002 的作用。在特异性蛋白激酶 A(PKA)抑制剂 H-89 的存在下,未观察到蜱唾液诱导的 IL-10 增强,这表明 PKA 途径参与了 IL-10 的产生。我们的累积数据表明,蜱唾液干扰了几种信号通路,从而调节了树突状细胞的免疫功能。

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