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Altered Molecular Expression of the TLR4/NF-κB Signaling Pathway in Mammary Tissue of Chinese Holstein Cattle with Mastitis

机译:TLR4 /NF-κB信号通路在荷斯坦牛乳腺炎乳腺组织中的分子表达改变

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摘要

Toll-like receptor 4 (TLR4) mediated activation of the nuclear transcription factor κB (NF-κB) signaling pathway by mastitis initiates expression of genes associated with inflammation and the innate immune response. In this study, the profile of mastitis-induced differential gene expression in the mammary tissue of Chinese Holstein cattle was investigated by Gene-Chip microarray and bioinformatics. The microarray results revealed that 79 genes associated with the TLR4/NF-κB signaling pathway were differentially expressed. Of these genes, 19 were up-regulated and 29 were down-regulated in mastitis tissue compared to normal, healthy tissue. Statistical analysis of transcript and protein level expression changes indicated that 10 genes, namely TLR4, MyD88, IL-6, and IL-10, were up-regulated, while, CD14, TNF-α, MD-2, IL-β, NF-κB, and IL-12 were significantly down-regulated in mastitis tissue in comparison with normal tissue. Analyses using bioinformatics database resources, such as the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis and the Gene Ontology Consortium (GO) for term enrichment analysis, suggested that these differently expressed genes implicate different regulatory pathways for immune function in the mammary gland. In conclusion, our study provides new evidence for better understanding the differential expression and mechanisms of the TLR4 /NF-κB signaling pathway in Chinese Holstein cattle with mastitis.
机译:Toll样受体4(TLR4)介导的乳腺炎引起的核转录因子κB(NF-κB)信号通路的激活,启动了与炎症和先天免疫反应相关的基因的表达。在这项研究中,通过基因芯片芯片和生物信息学研究了乳腺炎引起的中国荷斯坦牛乳腺组织中差异基因表达的概况。基因芯片结果显示与TLR4 /NF-κB信号通路相关的79个基因被差异表达。与正常的健康组织相比,乳腺炎组织中有19个基因上调,有29个基因下调。转录本和蛋白质水平表达变化的统计分析表明,TLR4,MyD88,IL-6和IL-10等10个基因上调,而CD14,TNF-α,MD-2,IL-β,NF与正常组织相比,乳腺炎组织中的-κB和IL-12明显下调。使用生物信息学数据库资源进行分析,例如《京都基因与基因组百科全书》(KEGG)途径分析和基因本体学联盟(GO)进行术语富集分析,表明这些表达不同的基因暗示了乳腺免疫功能的不同调控途径。 。总之,我们的研究为更好地了解中国荷斯坦奶牛乳腺炎TLR4 /NF-κB信号通路的差异表达及其机制提供了新的证据。

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