Impaired systemic proteostasis and peripheral immune cell dysfunction in kidney diseases

Bartolini Desirée, Migni Anna, Russo Roberta, G. Francesco
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Abstract

Kidney diseases, encompassing a spectrum of either acute or chronic disorders, manifest complex systemic repercussions beyond renal dysfunction. These include a reduced efficacy of tissue proteostasis mechanisms to control protein synthesis, folding, and degradation in both the renal and extra-renal compartments. Emerging research has revealed a pivotal interplay between proteostasis and immune regulation in the pathogenesis of kidney diseases, along with their cardiovascular, immunometabolic, and organ dysfunction symptoms. This review outlines the multifaceted connections between proteostasis dysregulation and immune dysfunction in kidney disease onset and progression. The crosstalk between the proteostasis network and immune cells orchestrates a bidirectional communication that amplifies pathological cascades, exacerbating kidney injury and impairing organ resilience. Furthermore, the article focuses on the implications of systemic proteostasis defects in modulating immune responses in extra-renal tissues underscore the systemic nature of kidney diseases. The disruption of proteostasis mechanisms triggers the release of damage-associated molecular patterns (DAMPs) and inflammatory mediators, perpetuating a state of heightened immune activation, contributing to systemic complications in affected individuals. Understanding the intricate interaction between proteostasis and immune regulation in kidney diseases, including both chronic and acute forms, promises novel therapeutic interventions. Targeting proteostasis pathways to restore cellular homeostasis and modulating immune responses could offer innovative strategies to mitigate renal damage and ameliorate systemic complications associated with kidney diseases. Harnessing this knowledge may also pave the way for the development of more efficient dialysis therapies and interventions with sorbents and hemoperfusion methods, to improve the clinical outcome of the patients.
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肾脏疾病中的全身蛋白稳态受损和外周免疫细胞功能障碍
肾脏疾病包括一系列急性或慢性疾病,除肾功能障碍外,还表现出复杂的全身影响。这些影响包括组织蛋白稳态机制控制肾脏和肾脏外区域蛋白质合成、折叠和降解的功效降低。新的研究揭示了蛋白稳态和免疫调节在肾脏疾病发病机制中的关键作用,以及心血管、免疫代谢和器官功能障碍症状。本综述概述了蛋白稳态失调与免疫功能障碍在肾病发病和进展过程中的多方面联系。蛋白稳态网络和免疫细胞之间的串联协调了一种双向交流,放大了病理级联,加剧了肾脏损伤,损害了器官的恢复能力。此外,文章还重点探讨了系统性蛋白稳态缺陷在调节肾外组织免疫反应方面的影响,强调了肾脏疾病的系统性。蛋白稳态机制的破坏会引发损伤相关分子模式(DAMPs)和炎症介质的释放,使免疫激活状态持续升高,从而导致患者出现全身性并发症。了解肾脏疾病(包括慢性和急性肾脏疾病)中蛋白稳态与免疫调节之间错综复杂的相互作用,有助于采取新的治疗干预措施。以蛋白稳态通路为靶点恢复细胞稳态和调节免疫反应,可为减轻肾脏损伤和改善与肾脏疾病相关的全身并发症提供创新策略。利用这些知识还可以为开发更有效的透析疗法以及使用吸附剂和血液灌流方法进行干预铺平道路,从而改善患者的临床疗效。
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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