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Aging and SKN-1-dependent Loss of 20S Proteasome Adaptation to Oxidative Stress in C. elegans

机译:老化和SKN-1依赖性损失20S蛋白酶体适应C.秀丽隐杆线的氧化胁迫

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摘要

Aging is marked by a collapse of protein homeostasis and deterioration of adaptive stress responses that often lead to disease. During aging, the induction of stress responses decline along with protein quality control. Here, we have shown that the ability to mount an adaptive response by pretreatment with minor oxidative stress is abrogated in aged Caenorhabditis elegans. We have identified a defect in SKN-1 signaling sensitivity during aging and have also found an aging-related increase in basal proteasome expression and in vitro activity, however, adaptation of the 20S proteasome in response to stress is lost in old animals. Interestingly, increased activation of SKN-1 promotes stress resistance, but is unable to rescue declining adaptation during aging. Our data demonstrate that the aging-dependent decline in SKN-1 signaling negatively impacts adaptation of the 20S proteasome in response to acute oxidative stress.
机译:衰老标志着蛋白质稳态和往往导致疾病的适应性应激反应的恶化。 在衰老期间,应力反应的诱导随着蛋白质质量控制而下降。 在这里,我们已经表明,通过用轻微的氧化应激预处理安装适应性响应的能力在老年人杆菌中消除了秀丽杆菌。 我们在老化期间鉴定了SKN-1信号感敏感性的缺陷,并且还发现基础蛋白酶体表达和体外活性的衰老增加,然而,在旧动物中丢失20S蛋白酶的适应性。 有趣的是,SKN-1的激活增加促进了应力阻力,但在老龄化期间无法抢救适应性下降。 我们的数据表明,SKN-1信号依赖性下降的依赖性下降对20S蛋白酶响应于急性氧化应激的调整产生负面影响。

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