Open AccessA peroxiredoxin, PRDX ‐2, is required for insulin secretion and insulin/ IIS ‐dependent regulation of stress resistance and longevity
Author(s) -
Oláhová Monika,
Veal Elizabeth A.
Publication year - 2015
Publication title -
aging cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.103
H-Index - 140
eISSN - 1474-9726
pISSN - 1474-9718
DOI - 10.1111/acel.12321
Subject(s) - peroxiredoxin , biology , caenorhabditis elegans , microbiology and biotechnology , downregulation and upregulation , insulin resistance , mutant , secretion , insulin receptor , insulin , biochemistry , gene , endocrinology , peroxidase , enzyme
Summary Peroxiredoxins (Prx) are abundant thiol peroxidases with a conserved anti‐ageing role. In contrast to most animals, the nematode worm, C aenorhabditis elegans , encodes a single cytosolic 2‐Cys Prx, PRDX ‐2, rendering it an excellent model for examining how peroxiredoxins affect animal physiology and ageing. Our previous work revealed that, although PRDX ‐2 protects against the toxicity of peroxides, enigmatically, prdx‐ 2‐mutant animals are hyper‐resistant to other forms of oxidative stress. Here, we have investigated the basis for this increased resistance. Mammalian FOXO and Nrf2 transcription factors directly promote the expression of a range of detoxification enzymes. We show that the FOXO orthologue, DAF ‐16, and the Nrf2 orthologue, SKN ‐1, are required for the increased stress resistance of prdx‐2 ‐mutant worms. Our data suggest that PRDX ‐2 is required for normal levels of insulin secretion and hence the inhibition of DAF ‐16 and SKN ‐1 by insulin/ IGF ‐1‐like signalling ( IIS ) under nutrient‐rich conditions. Intriguingly, loss of PRDX ‐2 increases DAF ‐16 and SKN ‐1 activities sufficiently to increase arsenite resistance without initiating other IIS ‐inhibited processes. Together, these data suggest that loss of peroxiredoxin function may increase stress resistance by reducing insulin secretion, but that further changes in insulin signalling are required for the reprogramming of development and fat metabolism. In addition, we reveal that the temperature‐dependent prolongevity function of PRDX ‐2 is required for the extended lifespan associated with several pathways, including further reductions in IIS .