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A Cell-penetrating Peptide Suppresses Inflammation by Inhibiting NF-κB Signaling

机译:穿透细胞的肽通过抑制NF-κB信号传导抑制炎症

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摘要

Nuclear factor-κB (NF-κB) is a central regulator of immune response and a potential target for developing anti-inflammatory agents. Mechanistic studies suggest that compounds that directly inhibit NF-κB DNA binding may block inflammation and the associated tissue damage. Thus, we attempted to discover peptides that could interfere with NF-κB signaling based on a highly conserved DNA-binding domain found in all NF-κB members. One such small peptide, designated as anti-inflammatory peptide-6 (AIP6), was characterized in the current study. AIP6 directly interacted with p65 and displayed an intrinsic cell-penetrating property. This peptide demonstrated significant anti-inflammatory effects in vitro and in vivo. In vitro, AIP6 inhibited the DNA-binding and transcriptional activities of the p65 NF-κB subunit as well as the production of inflammatory mediators in macrophages upon stimulation. Local administration of AIP6 significantly inhibited inflammation induced by zymosan in mice. Collectively, our results suggest that AIP6 is a promising lead peptide for the development of specific NF-κB inhibitors as potential anti-inflammatory agents.
机译:核因子-κB(NF-κB)是免疫应答的中央调节剂,是开发抗炎药的潜在靶标。机理研究表明,直接抑制NF-κBDNA结合的化合物可能会阻止炎症和相关的组织损伤。因此,我们试图基于在所有NF-κB成员中发现的高度保守的DNA结合结构域,发现可能干扰NF-κB信号传导的肽。在本研究中,对一种这样的小肽(称为抗炎肽6(AIP6))进行了表征。 AIP6直接与p65相互作用并显示出固有的细胞穿透特性。该肽在体外和体内表现出显着的抗炎作用。在体外,AIP6抑制p65NF-κB亚基的DNA结合和转录活性以及刺激后巨噬细胞中炎症介质的产生。 AIP6的局部给药可显着抑制酵母聚糖诱导的小鼠炎症。总的来说,我们的结果表明,AIP6是一种有前途的先导肽,可用于开发特定的NF-κB抑制剂作为潜在的抗炎药。

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