6-PPD quinone at environmentally relevant concentrations induces immunosenescenece by causing immunosuppression during the aging process.
Abstract
6-PPD quinone (6-PPDQ) could accelerate aging process. However, the underlying mechanism for the acceleration in aging process remains largely unclear. We aimed to examine the role of immunosuppression in 6-PPDQ in causing accelerated aging process in Caenorhabditis elegans. 6-PPDQ (0.1-10 μg/L) could decrease locomotion and increase reactive oxygen species (ROS) generation at both adult day-8 and day-12. 6-PPDQ at adult day-12 induced more severe immunosuppression reflected by decrease in expression of antimicrobial genes (lys-1, lys-7, spp-1, and dod-6) compared to that at adult day-8. Meanwhile, 6-PPDQ (10 μg/L) affected expressions of some transcriptional factor genes during the aging. Among them, at adult day-8, susceptibility to 6-PPDQ toxicity was caused by RNAi of daf-16, bar-1, elt-2, atf-7, skn-1, and nhr-8, and resistance to 6-PPDQ toxicity was induced by RNAi of daf-5, daf-3, and daf-12. Additionally, RNAi of daf-16, bar-1, elt-2, atf-7, skn-1, and nhr-8 caused more severe decrease in lys-1 and lys-7 expressions in 6-PPDQ exposed nematodes, whereas decrease in lys-1 and lys-7 expressions in 6-PPDQ exposed nematodes was inhibited by RNAi of daf-5, daf-3, and daf-12. The 6-PPDQ toxicity and 6-PPDQ induced decrease in lys-1 and lys-7 expressions were further suppressed by RNAi of insulin ligand genes (ins-6, ins-7, and daf-28) and receptor gene daf-2. Therefore, immunosuppression-caused immunosenescenece mediated the acceleration in aging process in 6-PPDQ exposed nematodes, which was under the control of certain transcriptional factors.
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Research summary
The paper investigates the role of 6-PPD quinone in inducing immunosenescence and its potential impact on the aging process in Caenorhabditis elegans. This focus on immunosuppression as a mechanism contributing to accelerated aging is relevant to longevity research. However, the findings appear to be incremental and primarily descriptive, lacking broader implications or novel insights that would significantly advance the field of aging research.
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