首页> 外文期刊>Chemical research in toxicology >Synergistic effects induced by a low dose of diesel particulate extract and ultraviolet-A in Caenorhabditis elegans: DNA damage-triggered germ cell apoptosis
【24h】

Synergistic effects induced by a low dose of diesel particulate extract and ultraviolet-A in Caenorhabditis elegans: DNA damage-triggered germ cell apoptosis

机译:低剂量柴油微粒提取物和紫外线-A对秀丽隐杆线虫的协同作用:DNA损伤触发的生殖细胞凋亡

获取原文
获取原文并翻译 | 示例
           

摘要

Diesel exhaust has been classified as a potential carcinogen and is associated with various health effects. A previous study showed that the doses for manifesting the mutagenetic effects of diesel exhaust could be reduced when coexposed with ultraviolet-A (UVA) in a cellular system. However, the mechanisms underlying synergistic effects remain to be clarified, especially in an in vivo system. In the present study, using Caenorhabditis elegans (C. elegans) as an in vivo system we studied the synergistic effects of diesel particulate extract (DPE) plus UVA, and the underlying mechanisms were dissected genetically using related mutants. Our results demonstrated that though coexposure of wild type worms at young adult stage to low doses of DPE (20 μg/mL) plus UVA (0.2, 0.5, and 1.0 J/cm2) did not affect worm development (mitotic germ cells and brood size), it resulted in a significant induction of germ cell death. Using the strain of hus-1::gfp, distinct foci of HUS-1::GFP was observed in proliferating germ cells, indicating the DNA damage after worms were treated with DPE plus UVA. Moreover, the induction of germ cell death by DPE plus UVA was alleviated in single-gene loss-of-function mutations of core apoptotic, checkpoint HUS-1, CEP-1/p53, and MAPK dependent signaling pathways. Using a reactive oxygen species (ROS) probe, it was found that the production of ROS in worms coexposed to DPE plus UVA increased in a time-dependent manner. In addition, employing a singlet oxygen (1O2) trapping probe, 2,2,6,6-tetramethyl-4-piperidone, coupled with electron spin resonance analysis, we demonstrated the increased 1O2 production in worms coexposed to DPE plus UVA. These results indicated that UVA could enhance the apoptotic induction of DPE at low doses through a DNA damage-triggered pathway and that the production of ROS, especially 1O2, played a pivotal role in initiating the synergistic process.
机译:柴油机废气已被归类为潜在的致癌物,并与各种健康影响相关。先前的研究表明,在细胞系统中与紫外线-A(UVA)共同暴露时,可以降低显示柴油机废气诱变效应的剂量。然而,协同作用的潜在机制仍有待阐明,特别是在体内系统中。在本研究中,使用秀丽隐杆线虫(C. elegans)作为体内系统,研究了柴油颗粒提取物(DPE)和UVA的协同效应,并使用相关突变体从遗传角度剖析了潜在的机制。我们的结果表明,虽然在成年期将野生型蠕虫与低剂量的DPE(20μg/ mL)和UVA(0.2、0.5和1.0 J / cm2)共同暴露不会影响蠕虫的发育(有丝分裂生殖细胞和育雏体大小) ),导致明显诱导生殖细胞死亡。使用hus-1 :: gfp菌株,在增殖的生殖细胞中观察到了HUS-1 :: GFP的明显病灶,表明蠕虫用DPE加UVA处理后对DNA的损害。此外,在核心凋亡,检查点HUS-1,CEP-1 / p53和MAPK依赖性信号通路的单基因功能丧失突变中,减轻了DPE加UVA诱导的生殖细胞死亡。使用活性氧(ROS)探针,发现与DPE和UVA共暴露的蠕虫中ROS的产生以时间依赖性方式增加。此外,使用单线态氧(1O2)捕获探针,2,2,6,6-四甲基-4-哌啶酮,再加上电子自旋共振分析,我们证明了与DPE和UVA共暴露的蠕虫中1O2产量增加。这些结果表明,UVA可以通过DNA损伤触发途径增强低剂量DPE的凋亡诱导作用,并且ROS(尤其是1O2)的产生在启动协同过程中起关键作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号