首页> 美国卫生研究院文献>Wiley-Blackwell Online Open >Leishmania donovani-induced expression of signal regulatory protein α on Kupffer cells enhances hepatic invariant NKT-cell activation
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Leishmania donovani-induced expression of signal regulatory protein α on Kupffer cells enhances hepatic invariant NKT-cell activation

机译:利什曼原虫引起的库普弗细胞信号调节蛋白α的表达增强肝恒定NKT细胞活化

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摘要

Signal regulatory protein α (SIRPα) and its cognate ligand CD47 have been documented to have a broad range of cellular functions in development and immunity. Here, we investigated the role of SIRPα–CD47 signalling in invariant NKT (iNKT) cell responses. We found that CD47 was required for the optimal production of IFN-γ from splenic iNKT cells following exposure to the αGalCer analogue PBS-57 and in vivo infection of mice with Leishmania donovani. Surprisingly, although SIRPα was undetectable in the liver of uninfected mice, the hepatic iNKT-cell response to infection was also impaired in CD47−/− mice. However, we found that SIRPα was rapidly induced on Kupffer cells following L. donovani infection, via a mechanism involving G-protein-coupled receptors. Thus, we describe a novel amplification pathway affecting cytokine production by hepatic iNKT cells, which may facilitate the breakdown of hepatic tolerance after infection.
机译:信号调节蛋白α(SIRPα)及其同源配体CD47已被证明在发育和免疫方面具有广泛的细胞功能。在这里,我们研究了SIRPα–CD47信号在不变NKT(iNKT)细胞反应中的作用。我们发现CD47是暴露于αGalCer类似物PBS-57和小鼠体内感染利什曼原虫后,从脾iNKT细胞中最佳产生IFN-γ所必需的。令人惊讶的是,尽管在未感染小鼠的肝脏中未检测到SIRPα,但在CD47 -/-小鼠中肝iNKT细胞对感染的反应也受损。然而,我们发现SIRPα是通过涉及G蛋白偶联受体的机制在L. donovani感染后在库普弗细胞上快速诱导的。因此,我们描述了一种新的扩增途径,其影响肝iNKT细胞产生的细胞因子,这可能有助于感染后肝耐受性的破坏。

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