Lippmann Juliane, Rothenburg Stefan, Deigendesch Nikolaus, Eitel Julia, Meixenberger Karolin, van Laak Vincent, Slevogt Hortense, N'guessan Philippe Dje, Hippenstiel Stefan, Chakraborty Trinad, Flieger Antje, Suttorp Norbert, Opitz Bastian
Department of Internal Medicine/Infectious Diseases and Pulmonary Medicine, Charité Universitätsmedizin Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.
Cell Microbiol. 2008 Dec;10(12):2579-88. doi: 10.1111/j.1462-5822.2008.01232.x. Epub 2008 Sep 2.
Intracellular bacteria and cytosolic stimulation with DNA activate type I IFN responses independently of Toll-like receptors, most Nod-like receptors and RIG-like receptors. A recent study suggested that ZBP1 (DLM-1/DAI) represents the long anticipated pattern recognition receptor which mediates IFNalpha/beta responses to cytosolic DNA in mice. Here we show that Legionella pneumophila infection, and intracellular challenge with poly(dA-dT), but not with poly(dG-dC), induced expression of IFNbeta, full-length hZBP1 and a prominent splice variant lacking the first Zalpha domain (hZBP1DeltaZalpha) in human cells. Overexpression of hZBP1 but not hZBP1DeltaZalpha slightly amplified poly(dA-dT)-stimulated IFNbeta reporter activation in HEK293 cells, but had no effect on IFNbeta and IL-8 production induced by bacteria or poly(dA-dT) in A549 cells. We found that mZBP1 siRNA impaired poly(dA-dT)-induced IFNbeta responses in mouse L929 fibroblasts at a later time point, while multiple hZBP1 siRNAs did not suppress IFNbeta or IL-8 expression induced by poly(dA-dT) or bacterial infection in human cells. In contrast, IRF3 siRNA strongly impaired the IFNbeta responses to poly(dA-dT) or bacterial infection. In conclusion, intracellular bacteria and cytosolic poly(dA-dT) activate IFNbeta responses in different human cells without requiring human ZBP1.
细胞内细菌以及DNA介导的胞质刺激可独立于Toll样受体、大多数Nod样受体和RIG样受体激活I型干扰素反应。最近的一项研究表明,ZBP1(DLM-1/DAI)代表了长期以来备受期待的模式识别受体,它介导小鼠对胞质DNA的IFNα/β反应。在此我们表明,嗜肺军团菌感染以及用聚(dA-dT)而非聚(dG-dC)进行细胞内刺激,可诱导人细胞中IFNβ、全长hZBP1以及一种缺少首个Zα结构域的显著剪接变体(hZBP1DeltaZalpha)的表达。hZBP1而非hZBP1DeltaZalpha的过表达在HEK293细胞中略微增强了聚(dA-dT)刺激的IFNβ报告基因激活,但对A549细胞中细菌或聚(dA-dT)诱导的IFNβ和IL-8产生没有影响。我们发现,mZBP1 siRNA在稍后时间点削弱了小鼠L929成纤维细胞中聚(dA-dT)诱导的IFNβ反应,而多种hZBP1 siRNA并未抑制人细胞中聚(dA-dT)或细菌感染诱导的IFNβ或IL-8表达。相比之下,IRF3 siRNA强烈削弱了对聚(dA-dT)或细菌感染的IFNβ反应。总之,细胞内细菌和胞质聚(dA-dT)在不同人细胞中激活IFNβ反应,而无需人ZBP1。