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P2X7受体介导的转谷氨酰胺酶2外化:与炎性关节炎有关联?

P2X7 receptor-mediated TG2 externalization: a link to inflammatory arthritis?

作者信息

Aeschlimann Daniel, Knäuper Vera

机构信息

Matrix Biology and Tissue Repair Research Unit, School of Dentistry, College of Biomedical and Life Sciences, Cardiff University, Heath Park, Cardiff, CF14 4XY, UK.

Arthritis Research UK Biomechanics and Bioengineering Centre of Excellence, College of Biomedical and Life Sciences, Cardiff University, The Sir Martin Evans Building, Museum Avenue, Cardiff, CF10 3AX, UK.

出版信息

Amino Acids. 2017 Mar;49(3):453-460. doi: 10.1007/s00726-016-2319-8. Epub 2016 Aug 25.

Abstract

Transglutaminases have important roles in stabilizing extracellular protein assemblies in tissue repair processes but some reaction products can stimulate immune activation, leading to chronic inflammatory conditions or autoimmunity. Exacerbated disease in models of inflammatory arthritis has been ascribed to sustained extracellular enzyme activity alongside formation of select protein modifications. Here, we review the evidence, with a focus on the link between P2X7R signaling and TG2 export, a pathway that we have recently discovered which ties extracellular protein modifications into the danger signal-mediated innate immune response. These recent insights offer new opportunities for therapeutic intervention.

摘要

转谷氨酰胺酶在组织修复过程中稳定细胞外蛋白质组装方面发挥着重要作用,但一些反应产物可刺激免疫激活,导致慢性炎症状态或自身免疫。炎症性关节炎模型中疾病的加剧被归因于持续的细胞外酶活性以及特定蛋白质修饰的形成。在此,我们回顾相关证据,重点关注P2X7R信号传导与TG2输出之间的联系,这是我们最近发现的一条将细胞外蛋白质修饰与危险信号介导的先天免疫反应联系起来的途径。这些最新见解为治疗干预提供了新机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a2f/5332493/09266dcbb27e/726_2016_2319_Fig1_HTML.jpg

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