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监测炎症小体激活的影像学方法。

Imaging Approaches to Monitor Inflammasome Activation.

机构信息

Department of Chemical Engineering, University of Massachusetts, Amherst, MA, USA; Department of Veterinary and Animal Sciences, University of Massachusetts, Amherst, MA, USA. Electronic address: https://twitter.com/dipikanandi24.

Department of Chemical Engineering, University of Massachusetts, Amherst, MA, USA. Electronic address: https://twitter.com/Shaheen30n.

出版信息

J Mol Biol. 2022 Feb 28;434(4):167251. doi: 10.1016/j.jmb.2021.167251. Epub 2021 Sep 17.

Abstract

Inflammasomes are a critical component of innate immune response which plays an important role in the pathogenesis of various chronic and acute inflammatory disease conditions. An inflammasome complex consists of a multimeric protein assembly triggered by any form of pathogenic or sterile insult, resulting in caspase-1 activation. This active enzyme is further known to activate downstream pro-inflammatory cytokines along with a pore-forming protein, eventually leading to a lytic cell death called pyroptosis. Understanding the spatiotemporal kinetics of essential inflammasome components provides a better interpretation of the complex signaling underlying inflammation during several disease pathologies. This can be attained via in-vitro and in-vivo imaging platforms, which not only provide a basic understanding of molecular signaling but are also crucial to develop and screen targeted therapeutics. To date, numerous studies have reported platforms to image different signaling components participating in inflammasome activation. Here, we review several elements of inflammasome signaling, a common molecular mechanism combining these elements and their respective imaging tools. We anticipate that future needs will include developing new inflammasome imaging systems that can be utilized as clinical tools for diagnostics and monitoring treatment responses.

摘要

炎症小体是先天免疫反应的关键组成部分,在各种慢性和急性炎症性疾病的发病机制中发挥重要作用。炎症小体复合物由多聚蛋白组装体组成,由任何形式的病原体或无菌损伤触发,导致半胱天冬酶-1 的激活。这种活性酶进一步被称为激活下游促炎细胞因子以及形成孔的蛋白,最终导致称为细胞焦亡的裂解性细胞死亡。了解必需炎症小体成分的时空动力学为在几种疾病病理中炎症下复杂信号的提供了更好的解释。这可以通过体外和体内成像平台来实现,这些平台不仅提供了对分子信号的基本理解,而且对于开发和筛选靶向治疗也至关重要。迄今为止,已有许多研究报道了用于成像参与炎症小体激活的不同信号成分的平台。在这里,我们回顾了炎症小体信号的几个要素,这些要素共同的分子机制以及它们各自的成像工具。我们预计未来的需求将包括开发新的炎症小体成像系统,这些系统可以用作诊断和监测治疗反应的临床工具。

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