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Identification of interferon-gamma-inducible-lysosomal thiol reductase (GILT) gene in goldfish (Carassius auratus) and its immune response to LPS challenge

机译:金鱼(Car鱼)中γ-干扰素诱导的溶酶体巯基还原酶(GILT)基因的鉴定及其对LPS攻击的免疫反应

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The interferon-gamma-inducible lysosomal thiol reductase (GILT) has been demonstrated to play an important role in the processing and presentation of MHC class II restricted antigen (Ag) by catalyzing disulfide bond reduction. In this study, we cloned a GILT gene homolog from goldfish (designated gGILT), a kind of precious freshwater fish with high market value. The open reading frame of gGILT consists of 756 bases encoding a protein of 251 amino acids with an estimated molecular mass of 27.8 kDa and a theoretical isoelectric point of 5.24. The deduced protein possesses the typical structural features of known GILT proteins, including an active-site motif, a GILT signature sequence, and 10 conserved cysteines. RT-PCR results showed that gGILT and gIFN-gamma (goldfish IFN-gamma) mRNA were expressed in a tissue-specific manner and obviously up-regulated in splenocytes and the cells from head kidney after induction with LPS. Recombinant gGILT fused with His6 tag was efficiently expressed in Escherichia coli BL21 (DE3) and purified by Ni-NTA affinity chromatography. Further study revealed that gGILT was capable of catalyzing the reduction of the interchain disulfide bonds from intact IgG. This study shows that gGILT may be involved in the immune response to bacteria challenge and maintain first line of innate immune defense at basal level in goldfish. It also provides the basis for investigating on the role of GILT using goldfish as an animal model. (C) 2014 Elsevier Ltd. All rights reserved.
机译:干扰素-γ诱导的溶酶体巯基还原酶(GILT)已被证明通过催化二硫键的还原在MHC II类限制性抗原(Ag)的加工和呈递中起重要作用。在这项研究中,我们从金鱼(称为gGILT)中克隆了GILT基因同源物,这是一种具有很高市场价值的珍贵淡水鱼。 gGILT的开放阅读框由756个碱基组成,编码251个氨基酸的蛋白质,估计分子量为27.8 kDa,理论等电点为5.24。推导的蛋白质具有已知GILT蛋白质的典型结构特征,包括活性位点基序,GILT签名序列和10个保守的半胱氨酸。 RT-PCR结果显示,LPS诱导后,脾脏细胞和头肾细胞中gGILT和gIFN-γ(金鱼IFN-γ)mRNA以组织特异性方式表达,并明显上调。与His6标签融合的重组gGILT在大肠杆菌BL21(DE3)中有效表达,并通过Ni-NTA亲和层析纯化。进一步的研究表明,gGILT能够催化完整IgG还原链间二硫键。这项研究表明,gGILT可能参与了对细菌攻击的免疫反应,并在金鱼的基础水平上维持了固有免疫防御的第一线。它还为研究使用金鱼作为动物模型的GILT的作用提供了基础。 (C)2014 Elsevier Ltd.保留所有权利。

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