Involvement of S100A8 and S100A9 in nonischaemic cardiomyopathy

Qiu-Yue Lin, Wen-Xi Jiang, Hui-Hua Li
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Abstract

The heterodimeric complex of S100 calcium binding proteins A8 and A9 (S100A8/A9, also known as Calprotectin) is constitutively expressed in myeloid neutrophils and monocytes and plays a role in the modulation of the inflammatory response and cytoskeleton rearrangement. Recently, S100A8/A9 complex has garnered significant attention as a critical alarmin involved in regulating the pathogenesis of various inflammatory cardiovascular diseases, particularly nonischaemic cardiomyopathy (NICM). Furthermore, S100A8/A9 is reportedly associated with the pathophysiological processes of myocardial ischaemia‒reperfusion injury and has also been recognised as a predictor and a potential mediator of heart failure caused by acute myocardial infarction. Recent studies have attempted to provide a comprehensive and detailed overview of the involvement of the S100A8/A9 protein in NICM, covering topics such as hypertrophic myocardial remodelling, septic and dilated cardiomyopathy, myocarditis, chemotherapeutic cardiotoxicity, senescent cardiac dysfunction and cardiac allograft rejection. Ultimately, we aimed to evaluate the application of S100A8/A9 as promising biomarkers and therapeutic strategies for the prediction, prevention and treatment of NICM.

Abstract Image

S100A8和S100A9参与非缺血性心肌病
S100钙结合蛋白A8和A9的异二聚体复合体(S100A8/A9,也称为钙保护蛋白)在髓系中性粒细胞和单核细胞中组成性表达,并在炎症反应和细胞骨架重排的调节中发挥作用。最近,S100A8/A9复合物作为一个重要的警报蛋白,参与调节各种炎症性心血管疾病,特别是非缺血性心肌病(NICM)的发病机制,引起了人们的广泛关注。此外,据报道,S100A8/A9与心肌缺血-再灌注损伤的病理生理过程有关,也被认为是急性心肌梗死引起心力衰竭的预测因子和潜在介质。最近的研究试图全面详细地概述S100A8/A9蛋白在NICM中的作用,涵盖肥厚性心肌重构、脓毒性和扩张性心肌病、心肌炎、化疗性心脏毒性、衰老性心功能障碍和心脏异体移植排斥反应等主题。最后,我们旨在评估S100A8/A9作为有前景的生物标志物和治疗策略在NICM预测、预防和治疗中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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