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Toll-8/Tollo Negatively Regulates Antimicrobial Response in the Drosophila Respiratory Epithelium

机译:Toll-8 / Tollo负调节果蝇呼吸上皮细胞的抗菌反应。

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摘要

Barrier epithelia that are persistently exposed to microbes have evolved potent immune tools to eliminate such pathogens. If mechanisms that control Drosophila systemic responses are well-characterized, the epithelial immune responses remain poorly understood. Here, we performed a genetic dissection of the cascades activated during the immune response of the Drosophila airway epithelium i.e. trachea. We present evidence that bacteria induced-antimicrobial peptide (AMP) production in the trachea is controlled by two signalling cascades. AMP gene transcription is activated by the inducible IMD pathway that acts non-cell autonomously in trachea. This IMD-dependent AMP activation is antagonized by a constitutively active signalling module involving the receptor Toll-8/Tollo, the ligand Spätzle2/DNT1 and Ect-4, the Drosophila ortholog of the human Sterile alpha and HEAT/ARMadillo motif (SARM). Our data show that, in addition to Toll-1 whose function is essential during the systemic immune response, Drosophila relies on another Toll family member to control the immune response in the respiratory epithelium.
机译:持续暴露于微生物的屏障上皮已经进化出有效的免疫工具来消除此类病原体。如果控制果蝇全身反应的机制被很好地表征,那么对上皮的免疫反应仍然知之甚少。在这里,我们对果蝇气道上皮即气管的免疫反应过程中激活的叶栅进行了遗传解剖。我们目前的证据表明,气管中细菌诱导的抗菌肽(AMP)的生产是由两个信号级联控制的。 AMP基因转录被可诱导的IMD途径激活,该途径在气管中自主发挥非细胞作用。这种IMD依赖的AMP激活被涉及受体Toll-8 / Tollo,配体Spätzle2/ DNT1和Ect-4,人不育α的果蝇直系同源物和HEAT / ARMadillo模体(SARM)的组成型活性信号传导模块拮抗。我们的数据表明,除了Toll-1(其功能在全身免疫应答中至关重要)之外,果蝇还依赖于另一个Toll家族成员来控制呼吸道上皮细胞的免疫应答。

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