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Regulation of Toll-like Receptor 5 Gene Expression and Function on Mucosal Dendritic Cells

机译:Toll样受体5基因表达和黏膜树突状细胞功能的调节。

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摘要

Toll-like receptor (TLR) 5 has been shown to maintain intestinal homeostasis and regulate host defense against enterobacterial infection. However, how TLR5 expression is regulated and its function in the intestine have not been fully elucidated. Here we demonstrate that mucosal dendritic cells (DCs), but not splenic DCs, express high levels of TLR5 protein. Alternatively spliced Tlr5 transcripts were identified but it did not explain the selective expression of TLR5 on mucosal DCs. Treatment with various bacterial ligands downregulated BMDC TLR5 expression, while retinoic acid and host stromal cell-derived signals promoted TLR5 expression in a TGF-β-independent mechanism. Signaling through TLR5 restrained regulatory T (Treg) cell generation, and accordingly, TLR5−/− mice displayed increased frequencies of Foxp3+ Treg cells in the intestinal lamina propria. Our data indicate that bacterial and host factors differentially regulate DC TLR5 expression. TLR5 signaling regulates immune responses towards the microbiota via modulation of the Treg/effector T cell balance.
机译:Toll样受体(TLR)5已显示维持肠道稳态并调节宿主抵抗肠细菌感染的防御能力。但是,TLR5表达如何在肠道中调节及其功能尚未完全阐明。在这里,我们证明粘膜树突状细胞(DCs),而不是脾脏DCs,表达高水平的TLR5蛋白。鉴定出剪接的剪接的Tlr5转录物,但不能解释TLR5在粘膜DC上的选择性表达。各种细菌配体的处理下调了BMDC TLR5的表达,而视黄酸和宿主基质细胞衍生的信号以TGF-β依赖性机制促进TLR5的表达。通过TLR5发出的信号抑制了调节性T(Treg)细胞的产生,因此,TLR5-/-小鼠在固有固有层中显示出Foxp3 + Treg细胞频率增加。我们的数据表明细菌和宿主因素差异调节DC TLR5表达。 TLR5信号传导通过调节Treg /效应子T细胞平衡来调节对微生物群的免疫反应。

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