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日本牙鲆(Paralichthys olivaceus)中双特异性丝裂原活化蛋白激酶磷酸酶6基因(dusp6)对免疫刺激的识别及功能分析

Identification and functional analysis of dual-specificity MAP kinase phosphatase 6 gene (dusp6) in response to immune challenges in Japanese flounder Paralichthys olivaceus.

作者信息

Li Shuo, Peng Weijiao, Hao Gaixiang, Li Jiafang, Geng Xuyun, Sun Jinsheng

机构信息

Tianjin Key Laboratory of Animal and Plant Resistance, College of Life Sciences, Tianjin Normal University, 393 West Binshui Road, Xiqing District, Tianjin 300387, China.

Tianjin Key Laboratory of Animal and Plant Resistance, College of Life Sciences, Tianjin Normal University, 393 West Binshui Road, Xiqing District, Tianjin 300387, China.

出版信息

Fish Shellfish Immunol. 2017 Jan;60:411-419. doi: 10.1016/j.fsi.2016.12.008. Epub 2016 Dec 8.

Abstract

Dual-specificity phosphatase 6 (Dusp6) is a member of mitogen-activated protein kinase (MAPK) phosphatases that play crucial roles in regulating MAPK signaling and immune response. The immunological relevance of Dusp6 in fish, however, remains largely uncharacterized. In the present study, a full-length Japanese flounder dusp6 cDNA ortholog, termed PoDusp6, was identified and characterized from Paralichthys olivaceus. The deduced PoDusp6 protein is comprised of 383 amino acids with a conserved N-terminal regulatory rhodanese homology domain and a C-terminal catalytic domain. Immunofluorescence microscopy revealed that PoDusp6 protein is mainly localized in cytoplasm. Sequence analysis indicates that PoDusp6 is highly conserved (>70% identity) throughout the evolution from teleost to mammals. In unstimulated conditions, PoDusp6 mRNA was present in all examined tissues and showed the highest expression in Japanese flounder head kidney macrophages (HKMs). Immune challenge experiments revealed that the expression of PoDusp6 was down-regulated at the early stage after LPS and poly(I:C) stimulations but significantly up-regulated at the later stage in the HKMs. The similar expression pattern was also observed in the Japanese flounder immune-related tissues including head kidney, gill and spleen upon bacterial challenge with Edwardsiella tarda. Overexpression of PoDusp6 in Japanese flounder FG-9307 cells led to a significant down-regulation of proinflammatory cytokine genes IL-1beta, TNF-alpha and IFN-gamma, and antiviral gene Mx. Interestingly, inhibition of Dusp6 activity also down-regulated the LPS-induced IL-beta gene expression but did not affected on the LPS-induced IFN-gamma and TNF-alpha expression in the HKMs. Our findings suggest that the expression of PoDusp6 is modulated by immune stimuli and PoDusp6 may act as an essential modulator in fish inflammatory response.

摘要

双特异性磷酸酶6(Dusp6)是丝裂原活化蛋白激酶(MAPK)磷酸酶家族的一员,在调节MAPK信号传导和免疫反应中发挥关键作用。然而,Dusp6在鱼类中的免疫学相关性在很大程度上仍未得到充分研究。在本研究中,从褐牙鲆(Paralichthys olivaceus)中鉴定并表征了一个全长的日本牙鲆dusp6 cDNA直系同源物,命名为PoDusp6。推导的PoDusp6蛋白由383个氨基酸组成,具有保守的N端调节硫氧还蛋白同源结构域和C端催化结构域。免疫荧光显微镜显示PoDusp6蛋白主要定位于细胞质中。序列分析表明,从硬骨鱼到哺乳动物的整个进化过程中,PoDusp6高度保守(同一性>70%)。在未刺激条件下,PoDusp6 mRNA存在于所有检测的组织中,并且在日本牙鲆头肾巨噬细胞(HKMs)中表达最高。免疫刺激实验表明,在HKMs中,LPS和聚肌苷酸-聚胞苷酸(poly(I:C))刺激后早期PoDusp6的表达下调,但后期显著上调。在用迟缓爱德华氏菌(Edwardsiella tarda)进行细菌攻击后,在日本牙鲆的免疫相关组织(包括头肾、鳃和脾脏)中也观察到了类似的表达模式。PoDusp6在日本牙鲆FG-9307细胞中的过表达导致促炎细胞因子基因IL-1β、TNF-α和IFN-γ以及抗病毒基因Mx的显著下调。有趣的是,抑制Dusp6活性也下调了HKMs中LPS诱导的IL-β基因表达,但对LPS诱导的IFN-γ和TNF-α表达没有影响。我们的研究结果表明,PoDusp6的表达受免疫刺激调节,并且PoDusp6可能在鱼类炎症反应中作为一种重要的调节因子发挥作用。

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