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.
Original language | English |
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Article number | 480 |
Journal | Frontiers in Molecular Neuroscience |
Volume | 11 |
DOIs | |
State | Published - 7 Jan 2019 |
Bibliographical note
Funding Information:The authors wish to thank Jessica Barrera for the graphic design of Figures 1 –3. Funding. This work was supported by a grant from the Canadian Institutes of Health Research (CIHR), the International Development Research Centre (IDRC), the Israel Science Foundation (ISF) and the Azrieli Foundation (ISF-IDRC 2395/2015 to KR); ISF 946/17 to KR, Israeli Ministry of Science, Technology, and Space (MOST 3-12080 and MOST 3-14761 to KR); TransNeuro ERANET JPND supported by the Israel Ministry of Health grant 3-14616 to KR; and ISF grant 1966/18 to ME.
Funding Information:
This work was supported by a grant from the Canadian Institutes of Health Research (CIHR), the International Development Research Centre (IDRC), the Israel Science Foundation (ISF) and the Azrieli Foundation (ISF-IDRC 2395/2015 to KR); ISF 946/17 to KR, Israeli Ministry of Science, Technology, and Space (MOST 3-12080 and MOST 3-14761 to KR); TransNeuro ERANET JPND
Publisher Copyright:
© 2019 Gal-Ben-Ari, Barrera, Ehrlich and Rosenblum.
Keywords
- Aging
- Alzheimer’s disease
- Cancer
- Learning and memory
- Metabolic stress
- PKR
- Protein synthesis
- Signal transduction
ASJC Scopus subject areas
- Molecular Biology
- Cellular and Molecular Neuroscience