Homeostasis control in health and disease by the unfolded protein response

IF 3.1 2区 化学 Q2 CHEMISTRY, ANALYTICAL
Diego Acosta-Alvear, Jonathan M. Harnoss, Peter Walter, Avi Ashkenazi
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引用次数: 0

Abstract

Cells rely on the endoplasmic reticulum (ER) to fold and assemble newly synthesized transmembrane and secretory proteins — essential for cellular structure–function and for both intracellular and intercellular communication. To ensure the operative fidelity of the ER, eukaryotic cells leverage the unfolded protein response (UPR) — a stress-sensing and signalling network that maintains homeostasis by rebalancing the biosynthetic capacity of the ER according to need. The metazoan UPR can also redirect signalling from cytoprotective adaptation to programmed cell death if homeostasis restoration fails. As such, the UPR benefits multicellular organisms by preserving optimally functioning cells while removing damaged ones. Nevertheless, dysregulation of the UPR can be harmful. In this Review, we discuss the UPR and its regulatory processes as a paradigm in health and disease. We highlight important recent advances in molecular and mechanistic understanding of the UPR that enable greater precision in designing and developing innovative strategies to harness its potential for therapeutic gain. We underscore the rheostatic character of the UPR, its contextual nature and critical open questions for its further elucidation.

Abstract Image

未折叠蛋白反应对健康和疾病的平衡控制
细胞依靠内质网(ER)来折叠和组装新合成的跨膜和分泌蛋白--这些蛋白对细胞结构-功能以及细胞内和细胞间的通讯都至关重要。为了确保ER的工作可靠性,真核细胞利用了未折叠蛋白反应(UPR)--一个压力传感和信号网络,通过根据需要重新平衡ER的生物合成能力来维持平衡。如果平衡恢复失败,元古动物的 UPR 还能将信号从细胞保护适应重新定向到程序性细胞死亡。因此,UPR 能在清除受损细胞的同时保留功能最佳的细胞,从而造福于多细胞生物。然而,UPR 的失调可能有害。在这篇综述中,我们将讨论作为健康和疾病范例的 UPR 及其调控过程。我们强调了最近在对 UPR 的分子和机理理解方面取得的重要进展,这些进展使我们能够更精确地设计和开发创新策略,以利用其治疗潜力。我们强调了 UPR 的流变特性、其背景性质以及有待进一步阐明的关键开放问题。
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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来源期刊
CiteScore
6.20
自引率
26.50%
发文量
228
审稿时长
1.7 months
期刊介绍: Innovative research on the fundamental theory and application of spectrometric techniques.
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