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免疫蛋白酶体抑制可减轻肿瘤坏死因子 α 刺激的肠上皮细胞中 NLRP3 炎性体的形成。

Inhibition of immunoproteasome attenuates NLRP3 inflammasome formation in tumor necrosis factor α-stimulated intestinal epithelial cell.

机构信息

Department of Bioscience and Biotechnology, Konkuk University, Neundong-ro 120, Gwangjin-gu, Seoul, 05029, Republic of Korea.

Department of Pharmaceutical Sciences, University of Kentucky, Lexington, KY, 40536-0596, United States.

出版信息

Biochem Biophys Res Commun. 2022 Oct 8;624:157-163. doi: 10.1016/j.bbrc.2022.07.120. Epub 2022 Aug 3.

Abstract

Excessive release of inflammatory cytokines has been considered as a major cause of chronic inflammation, resulting in intestinal barrier disruption that leads to inflammatory bowel disease (IBD). Tumor necrosis factor α (TNFα) is one of the well-known inflammatory cytokines that activates formation of NLRP3 inflammasome, thus resulting in excessive secretion of inflammatory cytokines causing IBD. Although immunoproteasome inhibitors have been reported to inhibit inflammatory cytokine release, immunoproteasome inhibition has not yet been addressed for attenuation of NLRP3 inflammasome activity in intestinal epithelial cell. Here, we observed that NLRP3 inflammasome assembly was attenuated by peptide epoxyketone YU102, a LMP2 subunit immunoproteasome inhibitor, in intestinal epithelial cell. YU102 also inhibited maturation of active caspase-1 and secretion of IL-1β, which are subsequent inflammatory cascade after the formation of NLRP3 inflammasome. Progression of epithelial-mesenchymal transition and increase of cellular permeability, which were induced by TNFα, were also suppressed through inhibition of immunoproteasome. Furthermore, we found that YU102 does not inhibit degradation of IкBα and its following NF-кB activation that leads to transcription of NLRP3. These findings suggest that inhibition of immunoproteasome with YU102 offers a potential therapeutic premise for prevention of TNFα-induced chronic inflammation through attenuation of NLRP3 inflammasome assembly.

摘要

过度释放炎症细胞因子被认为是慢性炎症的主要原因,导致肠道屏障破坏,从而引发炎症性肠病(IBD)。肿瘤坏死因子α(TNFα)是众所周知的炎症细胞因子之一,它激活 NLRP3 炎性体的形成,从而导致炎症性细胞因子的过度分泌,导致 IBD。虽然已经报道免疫蛋白酶体抑制剂可以抑制炎症细胞因子的释放,但尚未针对抑制免疫蛋白酶体来减轻肠道上皮细胞中 NLRP3 炎性体的活性。在这里,我们观察到 NLRP3 炎性体组装被免疫蛋白酶体抑制剂肽环氧酮 YU102 减弱,在肠道上皮细胞中。YU102 还抑制了活性半胱天冬酶-1的成熟和 IL-1β的分泌,这是 NLRP3 炎性体形成后的后续炎症级联。上皮-间充质转化的进展和细胞通透性的增加,这些都是由 TNFα 诱导的,也通过抑制免疫蛋白酶体而受到抑制。此外,我们发现 YU102 不会抑制 IкBα的降解及其随后的 NF-кB 激活,这导致了 NLRP3 的转录。这些发现表明,用 YU102 抑制免疫蛋白酶体通过减弱 NLRP3 炎性体组装,为预防 TNFα 诱导的慢性炎症提供了一种潜在的治疗前提。

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