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Inhibition of IRE1α RNase activity reduces NLRP3 inflammasome assembly and processing of pro-IL1β

机译:抑制IS1αRNase活性可降低NLRP3炎性组装和Pro-IL1β的加工

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摘要

The inflammasome is a multiprotein complex assembled in response to Pathogen Associated Molecular Patterns (PAMPs) and Danger Associated Molecular Patterns (DAMPs). Inflammasome activation occurs through a two-step mechanism, with the first signal facilitating priming of inflammasome components while the second signal triggers complex assembly. Once assembled, the inflammasome recruits and activates pro-caspase-1, which in turn processes pro-interleukin (IL)-18 and pro-IL-1β into their bio-active forms. Owing to its key role in the regulation of innate immune responses, the inflammasome has emerged as a therapeutic target for the treatment of inflammatory conditions. In this study we demonstrate that IRE1α, a key component of the Unfolded Protein Response, contributes to assembly of the NLRP3 inflammasome. Blockade of IRE1α RNase signaling lowered NLRP3 inflammasome assembly, caspase-1 activation and pro-IL-1β processing. These results underscore both the importance and potential therapeutic relevance of targeting IRE1α signaling in conditions of excessive inflammasome formation.
机译:炎性组是响应于病原体相关的分子模式(PAMP)和危险相关分子模式(潮湿)组装的多素蛋白复合物。发炎物激活通过两步机构发生,在第二信号触发复合组件时,第一信号促进炎性组件的灌注。一旦组装,炎性体新兵并激活Pro-Caspase-1,其依次将Pro-Interle蛋白(IL)-18和Pro-IL-1β加入其生物活性形式。由于其在对先天免疫应答的调节中作用的关键作用,炎性体已成为治疗炎性病症的治疗靶标。在该研究中,我们证明了展开蛋白质反应的关键组分,有助于组装NLRP3炎症。阻断IRE1αRNase信号传导降低NLRP3炎症组件,Caspase-1活化和Pro-IL-1β加工。这些结果强调了靶向IRE1α信号传导在过度炎症组形成条件下的重要性和潜在治疗相关性。

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