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Distinct chemokine and cytokine gene expression pattern of murine dendritic cells and macrophages in response to Mycobacterium tuberculosis infection

机译:结核分枝杆菌感染对小鼠树突状细胞和巨噬细胞不同趋化因子和细胞因子基因表达模式的影响

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摘要

In this study, the early innate cytokine and chemokine response of murine dendritic cells (DCs) and macrophages to Mycobacterium tuberculosis infection was compared. The findings indicate a dissimilar gene expression pattern between the two cell types. The expression of IL-12 and IL-23, important for promoting Th1 and Th17 cells, respectively, was up-regulated only in DCs. In addition, expression of CCL1 and CCL17, which are important in recruitment of T regulatory cells, was DC-specific, as was the expression of the immunosuppressive cytokine IL-10. Macrophages, in contrast, exhibited enhanced expression for CCL2 and CXCL10, chemokines that recruit cells to sites of inflammation, and for mycobactericidal molecules NO synthase 2 and TNF. Together, the findings suggest that a component of the innate DC response is not only programmed toward Th1 priming but is also for controlling the magnitude of the Th1 response, and part of the macrophage response is intended for recruiting cells to the lung and for mycobactericidal functions.
机译:在这项研究中,比较了小鼠树突状细胞(DC)和巨噬细胞对结核分枝杆菌感染的早期先天细胞因子和趋化因子反应。这些发现表明两种细胞类型之间的基因表达模式不同。 IL-12和IL-23的表达,分别对促进Th1和Th17细胞重要,仅在DC中上调。另外,在募集T调节细胞中很重要的CCL1和CCL17的表达是DC特异性的,免疫抑制细胞因子IL-10的表达也是如此。相反,巨噬细胞对CCL2和CXCL10,将细胞募集到炎症部位的趋化因子以及对分枝杆菌分子NO合酶2和TNF的表达增强。总之,这些发现表明,先天DC反应的一个组成部分不仅针对Th1引发进行编程,而且还用于控制Th1反应的强度,部分巨噬细胞反应旨在将细胞募集至肺部并用于分枝杆菌作用。 。

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