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Analysis of immune gene expression modulated by benzo[a]pyrene in head kidney of olive flounder (Paralichthys olivaceus)

机译:橄榄比目鱼头部肾脏中苯并[a] py调节的免疫基因表达分析

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Poly aromatic hydrocarbons (PAHs) are known to cause functional disorder of fish immune responses. Alteration of inflammatory cytokines and other immune gene expressions by PAHs in immune organs may play a pivotal role in immunotoxicity. Thus this study aimed to elucidate the immunotoxic mechanism of PAH using benzo[a]pyrene (BaP) by analyzing the gene expression of cytokines (IL-1β, TNFα, IL-6, IL-8, IFNγ, Mx), apoptosis (FasL, SOD) and other immune related substances (Lysozyme, IgM) in head kidney and macrophage in olive flounder. In Q-PCR analysis, proinflammatory cytokine (IL-1β, IL-6, IL-8, TNFα) gene expressions were significantly upregulated by BaP while Mx and IgM gene expressions were significantly downregulated in head kidney by a longer exposure to BaP in vivo and in vitro. Lysozyme gene expression was initially upregulated but later downregulated in head kidney in vivo and in vitro. Inhibition test revealed that TNFα gene expression was upregulated by BaP via the AHR pathway as blocked by ANF while IL-6 and IFNγ gene expressions were upregulated by a calcium dependent pathway (i.e. NFAT) as blocked by EGTA. In primary macrophage cells, only IL-8 gene expression was significantly upregulated among proinflammatory cytokines while IFNγ, lysozyme and IgM gene expressions were downregulated by BaP. FasL and SOD expressions were not altered in head kidney cells but significantly upregulated in macrophage cells, indicating apoptosis and oxidative stress. These results indicate that exposure to BaP causes the downregulation of immune response by triggering the death of macrophage cells, the reduction of effectors like IgM and lysozyme, and the decrease of macrophage cell activity.
机译:已知多芳烃(PAH)会导致鱼类免疫反应功能紊乱。 PAHs在免疫器官中改变炎症细胞因子和其他免疫基因表达可能在免疫毒性中起关键作用。因此,本研究旨在通过分析细胞因子(IL-1β,TNFα,IL-6,IL-8,IFNγ,Mx),细胞凋亡(FasL)的基因表达来阐明使用苯并[a] py(BaP)的PAH的免疫毒性机制。 ,SOD)和其他免疫相关物质(溶菌酶,IgM)位于头肾和比目鱼的巨噬细胞中。在Q-PCR分析中,BaP显着下调了头肾脏中促炎细胞因子(IL-1β,IL-6,IL-8,TNFα)的基因表达,而Mx和IgM基因的表达则在体内长期暴露于BaP的情况下显着下调。和体外。溶菌酶基因的表达最初在体内和体外在头肾中被上调,但随后被下调。抑制试验显示,BaP通过AHR途径通过AHR途径上调TNFα基因表达,而通过EGTA阻断钙依赖性途径(即NFAT)上调IL-6和IFNγ基因表达。在原代巨噬细胞中,促炎细胞因子中只有IL-8基因表达显着上调,而BaP下调了IFNγ,溶菌酶和IgM基因表达。 FasL和SOD的表达在头肾细胞中没有改变,但是在巨噬细胞中显着上调,表明细胞凋亡和氧化应激。这些结果表明,暴露于BaP会触发巨噬细胞死亡,IgM和溶菌酶等效应子的减少以及巨噬细胞活性的降低,从而引起免疫反应的下调。

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