Takase Hiroshi, Yu Cheng-Rong, Ham Don-Il, Chan Chi-Chao, Chen Jun, Vistica Barbara P, Wawrousek Eric F, Durum Scott K, Egwuagu Charles E, Gery Igal
Laboratory of Immunology, National Eye Institute, NIH, Building 10, 10 Center Drive, Bethesda, MD 20892-1857, USA.
J Leukoc Biol. 2006 Sep;80(3):538-45. doi: 10.1189/jlb.1205719. Epub 2006 Jun 22.
Immune cell-mediated inflammatory responses are triggered by TCR engagement with the target antigen, the initial event that brings about the complex sequence of events of the inflammatory process. Another form of inflammation is induced by local expression of certain cytokines. Unlike the former form of inflammation, little is known about the basic features of the cytokine-induced responses. Here, we analyzed tissue morphology, the infiltrating cells, and up-regulated, inflammation-related genes in mouse eyes in which inflammation is triggered by local transgenic (Tg) expression of cytokines and compared these features with those in eyes with experimental autoimmune uveitis (EAU), in which inflammation is initiated by engagement of TCR on sensitized T cells with their target antigen, followed by the well-defined, subsequent cytokine production. Eyes of IFN-gamma Tg mice exhibited severe, morphological changes but essentially no inflammation, and intense inflammation was found in eyes of interleukin (IL)-1 or IL-7 Tg mice. The cellular infiltration in eyes of these latter two lines of Tg mice resembled that in eyes with EAU by including many CD4 cells, but unlike in EAU, the infiltration in Tg eyes contained large proportions of B cells and only small numbers of macrophages. Real-time PCR analysis of eye RNA revealed differences among the disease models in the expression profiles of various inflammation-related genes. It is interesting that a bias toward T helper cell type 1 immunity (high IFN-gamma, RANTES/CCL5, MIG/CXCL9, and T-bet but low IL-4, IL-5, and GATA-3 transcripts) was found in EAU eyes but not in eyes of IL-1 and IL-7 Tg mice. The results thus show that similar to TCR engagement, local expression of certain cytokines triggers a complex, subsequent production of numerous inflammation-related molecules, but features of the ensued inflammatory process are determined by the triggering mechanism.
免疫细胞介导的炎症反应由TCR与靶抗原结合引发,这是引发炎症过程复杂事件序列的初始事件。另一种炎症形式由某些细胞因子的局部表达诱导。与前一种炎症形式不同,关于细胞因子诱导反应的基本特征知之甚少。在这里,我们分析了通过细胞因子局部转基因(Tg)表达引发炎症的小鼠眼睛的组织形态、浸润细胞和上调的炎症相关基因,并将这些特征与实验性自身免疫性葡萄膜炎(EAU)眼睛的特征进行了比较,在EAU中,炎症由致敏T细胞上的TCR与其靶抗原结合引发,随后是明确的后续细胞因子产生。干扰素-γTg小鼠的眼睛表现出严重的形态学变化,但基本没有炎症,而白细胞介素(IL)-1或IL-7Tg小鼠的眼睛发现有强烈炎症。后两种Tg小鼠品系眼睛中的细胞浸润与EAU眼睛中的相似,包括许多CD4细胞,但与EAU不同的是,Tg眼睛中的浸润含有大量B细胞和少量巨噬细胞。对眼睛RNA的实时PCR分析揭示了不同疾病模型中各种炎症相关基因表达谱的差异。有趣的是,在EAU眼睛中发现偏向于1型辅助性T细胞免疫(高干扰素-γ、RANTES/CCL5、MIG/CXCL9和T-bet转录本,但低IL-4、IL-5和GATA-3转录本),而在IL-1和IL-7Tg小鼠的眼睛中未发现。因此,结果表明,与TCR结合类似,某些细胞因子的局部表达会引发复杂的、随后大量炎症相关分子的产生,但随后炎症过程的特征由触发机制决定。