Wu Jingwei, Shen Shuhuai, Wang Dayong
Key Laboratory of Environmental Medicine Engineering of Ministry of Education, Medical School, Southeast University, Nanjing, China.
College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, China.
Chemosphere. 2024 Nov;368:143719. doi: 10.1016/j.chemosphere.2024.143719. Epub 2024 Nov 12.
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.
6-氨基-6-苯基-2,4-二羟基喹啉醌(6-PPDQ)可加速衰老进程。然而,其加速衰老进程的潜在机制仍 largely 不清楚。我们旨在研究免疫抑制在 6-PPDQ 导致秀丽隐杆线虫加速衰老过程中的作用。6-PPDQ(0.1 - 10μg/L)在成虫第 8 天和第 12 天均可降低运动能力并增加活性氧(ROS)生成。与成虫第 8 天相比,成虫第 12 天的 6-PPDQ 诱导更严重的免疫抑制,表现为抗菌基因(lys-1、lys-7、spp-1 和 dod-6)表达降低。同时,6-PPDQ(10μg/L)影响衰老过程中一些转录因子基因的表达。其中,在成虫第 8 天,daf-16、bar-1、elt-2、atf-7、skn-1 和 nhr-8 的 RNA 干扰导致对 6-PPDQ 毒性敏感,而 daf-5、daf-3 和 daf-12 的 RNA 干扰诱导对 6-PPDQ 毒性产生抗性。此外,daf-16、bar-1、elt-2、atf-7、skn-1 和 nhr-8 的 RNA 干扰导致暴露于 6-PPDQ 的线虫中 lys-1 和 lys-7 表达更严重下降,而 daf-5、daf-3 和 daf-12 的 RNA 干扰抑制了暴露于 6-PPDQ 的线虫中 lys-1 和 lys-7 表达的下降。胰岛素配体基因(ins-6、ins-7 和 daf-28)和受体基因 daf-2 的 RNA 干扰进一步抑制了 6-PPDQ 毒性以及 6-PPDQ 诱导的 lys-1 和 lys-7 表达下降。因此,免疫抑制导致的免疫衰老介导了暴露于 6-PPDQ 的线虫衰老进程的加速,这受某些转录因子的调控。