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Tissue expression of Toll-like receptors 2, 3, 4 and 7 in swine in response to the Shimen strain of classical swine fever virus

机译:猪的猪状猪瘟病毒的Shimen菌株的Toll样受体2,3,4和7的组织表达

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The Toll-like receptors (TLRs) of the innate immune system provide the host with the ability to detect and respond to viral infections. The present study aimed to investigate the mRNA and protein expression levels of TLR2, 3, 4 and 7 in porcine tissues upon infection with the highly virulent Shimen strain of classical swine fever virus (CSFV). Reverse transcription-quantitative polymerase chain reaction was used to detect the mRNA expression levels of CSFV and TLR, whereas western blotting was used to detect the expression levels of TLR proteins. In addition, tissues underwent histological examination and immunohistochemistry to reveal the histopathological alterations associated with highly virulent CSFV infection and to detect TLR antigens. Furthermore, porcine monocyte-derived macrophages (pMDMs) were prestimulated with peptidoglycan from Staphylococcus aureus (PGN-SA), polyinosinic-polycytidylic acid [poly (I:C)], lipopolysaccharide from Escherichia coli 055:B5 (LPS-B5) or imiquimod (R837) in order to analyze the association between TLR expression and CSFV replication. Following stimulation for 12 h (with TLR-specific ligands), cells were infected with CSFV Shimen strain. The results revealed that the expression levels of TLR2 and TLR4 were increased in the lung and kidney, but were decreased in the spleen and lymph nodes in response to CSFV. TLR3 was strongly expressed in the heart and slightly upregulated in the spleen in response to CSFV Shimen strain infection, and TLR7 was increased in all examined tissues in the presence of CSFV. Furthermore, R837 and LPS-B5 exerted inhibitory effects on CSFV replication in pMDMs, whereas PGN-SA and poly(I:C) had no significant effect. These findings highlight the potential role of TLR expression in the context of CSFV infection.
机译:先天免疫系统的收费受体(TLRS)提供了宿主,具有检测和响应病毒感染的能力。本研究旨在研究猪组织中TLR2,3,4和7的mRNA和蛋白表达水平在感染古典猪瘟病毒(CSFV)的高毒性雄月菌株时。逆转录定量聚合酶链反应检测CSFV和TLR的mRNA表达水平,而Western印迹用于检测TLR蛋白的表达水平。此外,组织接受组织学检查和免疫组织化学,以揭示与高毒力CSFV感染相关的组织病理学改变并检测TLR抗原。此外,猪单核细胞衍生的巨噬细胞(PMDMS)用来自金黄色葡萄球菌(PGN-SA)的肽聚糖(PGN-SA),来自大肠杆菌055(LPS-B5)或氨基末(LPS-B5)或咪喹啉(I:C)]的肽多糖[聚(I:C)],用肽聚糖衍生的巨噬细胞(PMDMS)。 (R837)为了分析TLR表达和CSFV复制之间的关联。在刺激12小时后(具有TLR特异性配体),细胞用CSFV Shimen菌株感染。结果表明,肺和肾的TLR2和TLR4的表达水平增加,但响应CSFV,脾脏和淋巴结中的脾脏和淋巴结减少。 TLR3在心脏中强烈表达,响应CSFV Shimen菌株感染的脾脏略微上调,并且在CSFV存在下所有检查的组织中,TLR7增加。此外,R837和LPS-B5对PMDMS中的CSFV复制施加抑制作用,而PGN-SA和Poly(I:C)没有显着效果。这些发现突出了TLR表达在CSFV感染情况下的潜在作用。

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