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PKR:一个值得铭记的激酶。

PKR: A Kinase to Remember.

作者信息

Gal-Ben-Ari Shunit, Barrera Iliana, Ehrlich Marcelo, Rosenblum Kobi

机构信息

Laboratory of Molecular and Cellular Mechanisms Underlying Learning and Memory, Sagol Department of Neurobiology, University of Haifa, Haifa, Israel.

Laboratory of Intracellular Trafficking and Signaling, School of Molecular Cell Biology & Biotechnology, The George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.

出版信息

Front Mol Neurosci. 2019 Jan 9;11:480. doi: 10.3389/fnmol.2018.00480. eCollection 2018.

Abstract

Aging is a major risk factor for many diseases including metabolic syndrome, cancer, inflammation, and neurodegeneration. Identifying mechanistic common denominators underlying the impact of aging is essential for our fundamental understanding of age-related diseases and the possibility to propose new ways to fight them. One can define aging biochemically as prolonged metabolic stress, the innate cellular and molecular programs responding to it, and the new stable or unstable state of equilibrium between the two. A candidate to play a role in the process is protein kinase R (PKR), first identified as a cellular protector against viral infection and today known as a major regulator of central cellular processes including mRNA translation, transcriptional control, regulation of apoptosis, and cell proliferation. Prolonged imbalance in PKR activation is both affected by biochemical and metabolic parameters and affects them in turn to create a feedforward loop. Here, we portray the central role of PKR in transferring metabolic information and regulating cellular function with a focus on cancer, inflammation, and brain function. Later, we integrate information from open data sources and discuss current knowledge and gaps in the literature about the signaling cascades upstream and downstream of PKR in different cell types and function. Finally, we summarize current major points and biological means to manipulate PKR expression and/or activation and propose PKR as a therapeutic target to shift age/metabolic-dependent undesired steady states.

摘要

衰老 是包括代谢综合征、癌症、炎症和神经退行性变在内的许多疾病的主要风险因素。确定衰老影响背后的机制共性对于我们从根本上理解与年龄相关的疾病以及提出对抗这些疾病的新方法至关重要。从生化角度来看,衰老可定义为长期的代谢应激、细胞和分子对其的固有反应程序,以及两者之间新的稳定或不稳定平衡状态。蛋白激酶R(PKR)可能在这一过程中发挥作用,它最初被鉴定为细胞抗病毒感染的保护因子,如今被认为是包括mRNA翻译、转录控制、细胞凋亡调节和细胞增殖在内的核心细胞过程的主要调节因子。PKR激活的长期失衡既受生化和代谢参数的影响,反过来又会影响这些参数,从而形成一个前馈回路。在这里,我们阐述PKR在传递代谢信息和调节细胞功能方面的核心作用,重点关注癌症、炎症和脑功能。随后,我们整合来自开放数据源的信息,并讨论文献中关于不同细胞类型和功能中PKR上下游信号级联的现有知识和空白。最后,我们总结当前操纵PKR表达和/或激活的主要要点和生物学方法,并提出将PKR作为一个治疗靶点,以改变年龄/代谢依赖性的不良稳态。

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