Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/5428
Title: Linking peroxiredoxin and vacuolar-ATPase functions in calorie restriction-mediated life span extension
Authors: Molin, Mikael
Demir, Ayşe Banu
Demir, Ayşe Banu
Keywords: Adenosine triphosphatase
Peroxiredoxin
Reactive oxygen metabolite
Calorie restriction
Free radical
Hydrogen peroxide
Iron metabolism
Issue Date: 2014
Publisher: Hindawi Publishing Corporation
Source: Molin, M., and Demir, A. B. (2014). Linking peroxiredoxin and vacuolar-ATPase functions in calorie restriction-mediated life span extension. International Journal of Cell Biology. doi:10.1155/2014/913071
Abstract: Calorie restriction (CR) is an intervention extending the life spans of many organisms. The mechanisms underlying CR-dependent retardation of aging are still poorly understood. Despite mechanisms involving conserved nutrient signaling pathways proposed, few target processes that can account for CR-mediated longevity have so far been identified. Recently, both peroxiredoxins and vacuolar-ATPases were reported to control CR-mediated retardation of aging downstream of conserved nutrient signaling pathways. In this review, we focus on peroxiredoxin-mediated stress-defence and vacuolar-ATPase regulated acidification and pinpoint common denominators between the two mechanisms proposed for how CR extends life span. Both the activities of peroxiredoxins and vacuolar-ATPases are stimulated upon CR through reduced activities in conserved nutrient signaling pathways and both seem to stimulate cellular resistance to peroxide-stress. However, whereas vacuolar-ATPases have recently been suggested to control both Ras-cAMP-PKA- and TORC1-mediated nutrient signaling, neither the physiological benefits of a proposed role for peroxiredoxins in H 2O2-signaling nor downstream targets regulated are known. Both peroxiredoxins and vacuolar-ATPases do, however, impinge on mitochondrial iron-metabolism and further characterization of their impact on iron homeostasis and peroxide-resistance might therefore increase our understanding of the beneficial effects of CR on aging and age-related diseases. © 2014 Mikael Molin and Ayse Banu Demir.
URI: http://doi.org/10.1155/2014/913071
http://hdl.handle.net/11147/5428
ISSN: 1687-8876
Appears in Collections:Molecular Biology and Genetics / Moleküler Biyoloji ve Genetik
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection

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