Jang Sihyug, Uzelac Aleksandra, Salgame Padmini
University of Medicine and Dentistry of New Jersey, Department of Medicine, Centre for Emerging Pathogens, Newark, NJ 07101, USA.
J Leukoc Biol. 2008 Nov;84(5):1264-70. doi: 10.1189/jlb.1107742. Epub 2008 Aug 14.
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.
在本研究中,比较了小鼠树突状细胞(DCs)和巨噬细胞对结核分枝杆菌感染的早期先天性细胞因子和趋化因子反应。研究结果表明这两种细胞类型之间存在不同的基因表达模式。分别对促进Th1和Th17细胞很重要的IL-12和IL-23的表达仅在DCs中上调。此外,对招募调节性T细胞很重要的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。相比之下,巨噬细胞对CCL2和CXCL10(将细胞招募到炎症部位的趋化因子)以及对杀分枝杆菌分子一氧化氮合酶2和肿瘤坏死因子的表达增强。总之,研究结果表明先天性DC反应的一个组成部分不仅针对Th1启动进行编程,而且还用于控制Th1反应的强度,巨噬细胞反应的一部分旨在将细胞招募到肺部并发挥杀分枝杆菌功能。