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牛分枝杆菌诱导的早期肉芽肿中 IL-17A、CXCL9 和 CXCL10 的上调。

Upregulation of IL-17A, CXCL9 and CXCL10 in early-stage granulomas induced by Mycobacterium bovis in cattle.

机构信息

TB Research Group, Department of Bacteriology, Animal Health and Veterinary Laboratories Agency, AHVLA - Weybridge, New Haw, Addlestone, Surrey, UK.

出版信息

Transbound Emerg Dis. 2013 Dec;60(6):525-37. doi: 10.1111/j.1865-1682.2012.01370.x. Epub 2012 Aug 22.

Abstract

To gain further insight into the immunopathogenesis of bovine tuberculosis (bTB), the cytokine and chemokine expression of cattle experimentally infected with Mycobacterium bovis was analysed in TB granulomas, using immunohistochemistry (IHC) and laser capture microdissection (LCM) followed by qPCR. Immunohistochemistry was conducted for cell types using labelling for CD68, CD3, CD4, CD8, WC1 and CD79a and for the cytokines IFN-γ, TNF-α and TGF-β as well as inducible form of nitric oxide synthase (iNOS). qPCR was conducted for mRNA expression of IFN-γ, TNF-α, TGF-β, IL-17A, IL-22, IL-2, granzyme A and the chemokines CXCL9 and CXCL10. Early stages of granuloma were primarily comprised of epithelioid MΦs expressing high levels of IFN-γ and iNOS, with significantly upregulated expression of CXCL9 and CXCL10 when compared with control tissue. These chemokines displayed a trend of decreasing mRNA expression as lesion progressed, suggesting a higher level of importance during the early stages of the immune response to mycobacterial infection. IL-22 levels showed a strong trend of decrease through granuloma development, and IL-17A was shown to be upregulated, supporting its investigation as a potential biomarker of bTB. The use of LCM and qPCR may prove especially useful for the study of IL-17A as previous attempts to analyse its expression using IHC and in situ hybridization proved unsuccessful.

摘要

为了更深入地了解牛结核病(bTB)的免疫发病机制,我们通过免疫组织化学(IHC)和激光捕获显微切割(LCM)联合 qPCR 分析了实验感染牛分枝杆菌的牛的 TB 肉芽肿中的细胞因子和趋化因子表达。使用 CD68、CD3、CD4、CD8、WC1 和 CD79a 对细胞类型进行免疫标记,并对 IFN-γ、TNF-α 和 TGF-β 以及诱导型一氧化氮合酶(iNOS)进行免疫组织化学染色。对 IFN-γ、TNF-α、TGF-β、IL-17A、IL-22、IL-2、颗粒酶 A 以及趋化因子 CXCL9 和 CXCL10 的 mRNA 表达进行了 qPCR 检测。肉芽肿的早期阶段主要由上皮样 MΦ 组成,这些细胞表达高水平的 IFN-γ 和 iNOS,与对照组织相比,CXCL9 和 CXCL10 的表达显著上调。与对照组织相比,这些趋化因子的 mRNA 表达随着病变的进展呈下降趋势,表明在针对分枝杆菌感染的免疫反应早期阶段,它们具有更高的重要性。IL-22 水平在肉芽肿发育过程中呈明显下降趋势,而 IL-17A 呈上调趋势,支持将其作为 bTB 的潜在生物标志物进行研究。LCM 和 qPCR 的使用可能对 IL-17A 的研究特别有用,因为之前使用 IHC 和原位杂交分析其表达的尝试均未成功。

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