Dewas Cedric, Chen Xi, Honda Tetsuya, Junttila Ilkka, Linton Jay, Udey Mark C, Porcella Stephen F, Sturdevant Daniel E, Feigenbaum Lionel, Koo Lily, Williams Joy, Paul William E
Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892;
Laboratory of Systems Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892;
J Immunol. 2015 Feb 1;194(3):1372-80. doi: 10.4049/jimmunol.1400519. Epub 2014 Dec 24.
Thymic stromal lymphopoietin (TSLP) is a type I cytokine that plays a central role in induction of allergic inflammatory responses. Its principal targets have been reported to be dendritic cells and/or CD4 T cells; epithelial cells are a principal source. We report in this study the development of a reporter mouse (TSLP-ZsG) in which a ZsGreen (ZsG)-encoding construct has been inserted by recombineering into a bacterial artificial chromosome immediately at the translation initiating ATG of TSLP. The expression of ZsG by mice transgenic for the recombinant BAC appears to be a faithful surrogate for TSLP expression, particularly in keratinocytes and medullary thymic epithelial cells. Limited ZsG and TSLP mRNA was observed in bone marrow-derived mast cells, basophils, and dendritic cells. Using the TSLP-ZsG reporter mouse, we show that TNF-α and IL-4/IL-13 are potent inducers of TSLP expression by keratinocytes and that local activation of Th2 and Th1 cells induces keratinocyte TSLP expression. We suggest that the capacity of TSLP to both induce Th2 differentiation and to be induced by activated Th2 cells raises the possibility that TSLP may be involved in a positive feedback loop to enhance allergic inflammatory conditions.
胸腺基质淋巴细胞生成素(TSLP)是一种I型细胞因子,在诱导过敏性炎症反应中起核心作用。据报道,其主要靶细胞是树突状细胞和/或CD4 T细胞;上皮细胞是主要来源。我们在本研究中报告了一种报告基因小鼠(TSLP-ZsG)的构建,其中通过重组工程将编码ZsGreen(ZsG)的构建体插入到紧邻TSLP翻译起始ATG的细菌人工染色体中。携带重组BAC的转基因小鼠中ZsG的表达似乎是TSLP表达的可靠替代指标,特别是在角质形成细胞和胸腺髓质上皮细胞中。在骨髓来源的肥大细胞、嗜碱性粒细胞和树突状细胞中观察到有限的ZsG和TSLP mRNA。使用TSLP-ZsG报告基因小鼠,我们发现TNF-α和IL-4/IL-13是角质形成细胞TSLP表达的有效诱导剂,并且Th2和Th1细胞的局部激活可诱导角质形成细胞TSLP表达。我们认为,TSLP既能诱导Th2分化又能被活化的Th2细胞诱导,这增加了TSLP可能参与正反馈回路以增强过敏性炎症状态的可能性。