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Molecular Control of Innate Immune Response to Pseudomonas aeruginosa Infection by Intestinal let-7 in Caenorhabditis elegans

机译:秀丽隐杆线虫肠let-7对铜绿假单胞菌感染的天然免疫应答的分子控制。

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摘要

The microRNA (miRNA) let-7 is an important miRNA identified in Caenorhabditis elegans and has been shown to be involved in the control of innate immunity. The underlying molecular mechanisms for let-7 regulation of innate immunity remain largely unclear. In this study, we investigated the molecular basis for intestinal let-7 in the regulation of innate immunity. Infection with Pseudomonas aeruginosa PA14 decreased let-7::GFP expression. Intestine- or neuron-specific activity of let-7 was required for its function in the regulation of innate immunity. During the control of innate immune response to P. aeruginosa PA14 infection, SDZ-24 was identified as a direct target for intestinal let-7. SDZ-24 was found to be predominantly expressed in the intestine, and P. aeruginosa PA14 infection increased SDZ-24::GFP expression. Intestinal let-7 regulated innate immune response to P. aeruginosa PA14 infection by suppressing both the expression and the function of SDZ-24. Knockout or RNA interference knockdown of sdz-24 dampened the resistance of let-7 mutant to P. aeruginosa PA14 infection. Intestinal overexpression of sdz-24 lacking 3’-UTR inhibited the susceptibility of nematodes overexpressing intestinal let-7 to P. aeruginosa PA14 infection. In contrast, we could observed the effects of intestinal let-7 on innate immunity in P. aeruginosa PA14 infected transgenic strain overexpressing sdz-24 containing 3’-UTR. In the intestine, certain SDZ-24-mediated signaling cascades were formed for nematodes against the P. aeruginosa PA14 infection. Our results highlight the crucial role of intestinal miRNAs in the regulation of the innate immune response to pathogenic infection.
机译:microRNA(miRNA)let-7是在秀丽隐杆线虫中鉴定出的重要miRNA,并已证明参与先天免疫的控制。 let-7调节先天性免疫的基本分子机制仍然不清楚。在这项研究中,我们调查了肠let-7在先天免疫调节中的分子基础。铜绿假单胞菌PA14感染降低let-7 :: GFP表达。 let-7在先天免疫调节中的功能需要肠道或神经元特异性活性。在控制对铜绿假单胞菌PA14感染的先天免疫反应期间,SDZ-24被确定为肠道let-7的直接靶标。发现SDZ-24主要在肠中表达,铜绿假单胞菌PA14感染增加了SDZ-24 :: GFP的表达。肠道let-7通过抑制SDZ-24的表达和功能来调节对铜绿假单胞菌PA14感染的先天免疫应答。 sdz-24 的敲除或RNA干扰敲除削弱了 let-7 突变体对 P 的抗性。 aeruginosa PA14感染。缺少3'-UTR的 sdz-24 肠道过度表达抑制了过度表达肠道 let-7 的线虫对 P 的敏感性。 aeruginosa PA14感染。相反,我们可以观察到肠道 let-7 P 中先天免疫的影响。过量表达 sdz-24 的含有3'-UTR的 aeruginosa PA14感染的转基因菌株。在肠道中,某些线虫形成了针对 P 的线虫SDZ-24介导的信号级联。 aeruginosa PA14感染。我们的结果突出了肠道miRNA在调节对病原体感染的先天免疫反应中的关键作用。

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