Roseman University of Health Sciences School of Pharmacy, 11 Sunset Way, Henderson, NV, 89014, USA.
Touro University Nevada, Henderson, NV, 89014, USA.
Cell Stress Chaperones. 2021 Jan;26(1):187-197. doi: 10.1007/s12192-020-01168-z. Epub 2020 Oct 16.
Survival and adaptation to oxidative stress is important for many organisms, and these occur through the activation of many different signaling pathways. In this report, we showed that Caenorhabditis (C.) elegans G protein-coupled receptor kinases modified the ability of the organism to resist oxidative stress. In acute oxidative stress studies using juglone, loss-of-function grk-2 mutants were more resistant to oxidative stress compared with loss-of-function grk-1 mutants and the wild-type N2 animals. This effect was Ce-AKT-1 dependent, suggesting that Ce-GRK2 adjusted C. elegans oxidative stress resistance through the IGF/insulin-like signaling (IIS) pathway. Treating C. elegans with a GRK2 inhibitor, the selective serotonin reuptake inhibitor paroxetine, resulted in increased acute oxidative stress resistance compared with another selective serotonin reuptake inhibitor, fluoxetine. In chronic oxidative stress studies with paraquat, both grk-1 and grk-2 mutants had longer lifespan compared with the wild-type N2 animals in stress. In summary, this research showed the importance of both GRKs, especially GRK2, in modifying oxidative stress resistance.
生存和适应氧化应激对于许多生物很重要,这是通过激活许多不同的信号通路来实现的。在本报告中,我们表明秀丽隐杆线虫(C. elegans)G 蛋白偶联受体激酶修饰了生物体抵抗氧化应激的能力。在使用胡桃醌的急性氧化应激研究中,与失活功能的 grk-1 突变体相比,失活功能的 grk-2 突变体对氧化应激更具抗性,而野生型 N2 动物则不具有这种抗性。这种效应依赖于 Ce-AKT-1,表明 Ce-GRK2 通过 IGF/胰岛素样信号(IIS)途径来调节秀丽隐杆线虫的氧化应激抗性。用 GRK2 抑制剂,选择性 5-羟色胺再摄取抑制剂帕罗西汀处理秀丽隐杆线虫,与另一种选择性 5-羟色胺再摄取抑制剂氟西汀相比,会导致急性氧化应激抗性增强。在用百草枯进行慢性氧化应激研究中,grk-1 和 grk-2 突变体在应激条件下的寿命均比野生型 N2 动物长。总之,这项研究表明了两种 GRK(尤其是 GRK2)在修饰氧化应激抗性方面的重要性。