The Duality of AIM2 Inflammasome: A Focus on its Role in Autoimmunity and Skin Diseases

M. Canavese
{"title":"The Duality of AIM2 Inflammasome: A Focus on its Role in Autoimmunity and Skin Diseases","authors":"M. Canavese","doi":"10.3844/AJPTSP.2016.8.19","DOIUrl":null,"url":null,"abstract":"Understanding the inflammasome biology is one of the most exciting challenges in immuno-pharmacology. The role of the inflammasomes has been recognized in the host defense mechanism against invading pathogens and in the development of several conditions, such as cancer, auto-inflammatory, autoimmune, metabolic and neurodegenerative disorders. DNA recognition by the cells is a crucial immunological step leading to the initiation of an innate immune response. Absent in Melanoma 2 (AIM2) is a cytoplasmic sensor that perceives double-stranded DNA of microbial or host origin. Once the DNA is bound, AIM2 assembles a multiprotein complex named inflammasome, which drives pyroptosis and proteolytic cleavage of pro-IL-1I² and pro-IL-18 pro-inflammatory cytokines, leading to a protective inflammasome-mediated host response. However, improper recognition of self-DNA by AIM2 triggers deleterious inflammatory responses, leading to systemic inflammation and several pathological conditions. Therefore, understanding the mechanisms of AIM2-inflammasome-mediated inflammation will provide an essential knowledge base to develop new successful therapeutic strategies to cure the outlined pathologies in which AIM2- inflammasome activation plays a key role, as well as to guide clinical practice. This mini-review provides an overview on the latest research findings on AIM2 inflammasome, with particular focus on its role in autoimmunity and skin disorders. An update on its therapeutic implications has also been documented.","PeriodicalId":7769,"journal":{"name":"American Journal of Pharmacology and Toxicology","volume":"33 1","pages":"8-19"},"PeriodicalIF":0.0000,"publicationDate":"2016-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Pharmacology and Toxicology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3844/AJPTSP.2016.8.19","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Understanding the inflammasome biology is one of the most exciting challenges in immuno-pharmacology. The role of the inflammasomes has been recognized in the host defense mechanism against invading pathogens and in the development of several conditions, such as cancer, auto-inflammatory, autoimmune, metabolic and neurodegenerative disorders. DNA recognition by the cells is a crucial immunological step leading to the initiation of an innate immune response. Absent in Melanoma 2 (AIM2) is a cytoplasmic sensor that perceives double-stranded DNA of microbial or host origin. Once the DNA is bound, AIM2 assembles a multiprotein complex named inflammasome, which drives pyroptosis and proteolytic cleavage of pro-IL-1I² and pro-IL-18 pro-inflammatory cytokines, leading to a protective inflammasome-mediated host response. However, improper recognition of self-DNA by AIM2 triggers deleterious inflammatory responses, leading to systemic inflammation and several pathological conditions. Therefore, understanding the mechanisms of AIM2-inflammasome-mediated inflammation will provide an essential knowledge base to develop new successful therapeutic strategies to cure the outlined pathologies in which AIM2- inflammasome activation plays a key role, as well as to guide clinical practice. This mini-review provides an overview on the latest research findings on AIM2 inflammasome, with particular focus on its role in autoimmunity and skin disorders. An update on its therapeutic implications has also been documented.
AIM2炎性小体的双重性:在自身免疫和皮肤疾病中的作用
了解炎性体生物学是免疫药理学中最令人兴奋的挑战之一。炎性小体的作用已被认识到在宿主防御入侵病原体的机制和几种疾病的发展中,如癌症、自身炎症、自身免疫、代谢和神经退行性疾病。细胞的DNA识别是导致先天免疫反应启动的关键免疫步骤。在黑色素瘤2 (AIM2)中缺失的是一种细胞质传感器,它可以感知微生物或宿主来源的双链DNA。一旦DNA被结合,AIM2就会组装一个名为炎性小体的多蛋白复合物,该复合物驱动前il - 1i²和前il -18促炎细胞因子的焦亡和蛋白水解裂解,从而导致炎性小体介导的保护性宿主反应。然而,AIM2对自身dna的错误识别会引发有害的炎症反应,导致全身性炎症和多种病理状况。因此,了解AIM2-炎性小体介导的炎症机制将为开发新的成功治疗策略提供必要的知识基础,以治愈AIM2-炎性小体激活起关键作用的概述病理,并指导临床实践。本文综述了AIM2炎性小体的最新研究成果,重点介绍了其在自身免疫和皮肤疾病中的作用。关于其治疗意义的最新情况也有文献记载。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信