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无菌性炎症小鼠模型中固有防御调节肽-1002抗炎活性的机制

Mechanisms of the Innate Defense Regulator Peptide-1002 Anti-Inflammatory Activity in a Sterile Inflammation Mouse Model.

作者信息

Wu Bing Catherine, Lee Amy Huei-Yi, Hancock Robert E W

机构信息

Centre for Microbial Diseases and Immunity Research, Department of Microbiology and Immunology, University of British Columbia, Vancouver, British Columbia V6T 1Z4, Canada.

Centre for Microbial Diseases and Immunity Research, Department of Microbiology and Immunology, University of British Columbia, Vancouver, British Columbia V6T 1Z4, Canada

出版信息

J Immunol. 2017 Nov 15;199(10):3592-3603. doi: 10.4049/jimmunol.1700985. Epub 2017 Oct 9.

Abstract

Innate defense regulator (IDR) peptide-1002 is a synthetic host defense peptide derivative with strong anti-inflammatory properties. Extending previous data, IDR-1002 suppressed in vitro inflammatory responses in RAW 264.7 murine monocyte/macrophage cells challenged with the TLR4 agonist LPS and TLR2 agonists lipoteichoic acid and zymosan. To investigate the anti-inflammatory mechanisms of IDR-1002 in vivo, the PMA-induced mouse ear inflammation model was used. Topical IDR-1002 treatment successfully dampened PMA-induced ear edema, proinflammatory cytokine production, reactive oxygen and nitrogen species release, and neutrophil recruitment in the ears of CD1 mice. Advanced RNA transcriptomic analysis on the mouse ear transcriptome revealed that IDR-1002 reduced sterile inflammation by suppressing the expression of transmembrane G protein-coupled receptors (class A/1 rhodopsin-like), including receptors for chemokines, PGs, histamine, platelet activating factor, and anaphylatoxin. IDR-1002 also dampened the IFN-γ response and repressed the IFN regulatory factor 8-regulated network that controls central inflammatory pathways. This study demonstrates that IDR-1002 exhibits strong in vitro and in vivo anti-inflammatory activities, informs the underlying anti-inflammatory mechanisms, and reveals its potential as a novel therapeutic for inflammatory diseases.

摘要

固有防御调节因子(IDR)肽-1002是一种具有强大抗炎特性的合成宿主防御肽衍生物。扩展先前的数据,IDR-1002抑制了用TLR4激动剂脂多糖(LPS)以及TLR2激动剂脂磷壁酸和酵母聚糖刺激的RAW 264.7小鼠单核细胞/巨噬细胞的体外炎症反应。为了研究IDR-1002在体内的抗炎机制,使用了佛波酯(PMA)诱导的小鼠耳部炎症模型。局部应用IDR-1002成功减轻了PMA诱导的CD1小鼠耳部水肿、促炎细胞因子产生、活性氧和氮物质释放以及中性粒细胞募集。对小鼠耳部转录组进行的高级RNA转录组分析显示,IDR-1002通过抑制跨膜G蛋白偶联受体(A类/1视紫红质样)的表达来减轻无菌性炎症,这些受体包括趋化因子、前列腺素、组胺、血小板活化因子和过敏毒素的受体。IDR-1002还减弱了IFN-γ反应,并抑制了控制中枢炎症途径的IFN调节因子8调控网络。本研究表明,IDR-1002在体外和体内均表现出强大的抗炎活性,阐明了其潜在的抗炎机制,并揭示了其作为炎症性疾病新型治疗药物的潜力。

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