首页> 外文期刊>Toxicology and Applied Pharmacology >PCB153 reduces telomerase activity and telomere length in immortalized human skin keratinocytes (HaCaT) but not in human foreskin keratinocytes (NFK)
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PCB153 reduces telomerase activity and telomere length in immortalized human skin keratinocytes (HaCaT) but not in human foreskin keratinocytes (NFK)

机译:PCB153降低永生化的人皮肤角质形成细胞(HaCaT)中的端粒酶活性和端粒长度,但不降低人的包皮角质形成细胞(NFK)中的端粒酶活性和端粒长度

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Polychlorinated biphenyls (PCBs), ubiquitous environmental pollutants, are characterized by long term-persistence in the environment, bioaccumulation, and biomagnification in the food chain. Exposure to PCBs may cause various diseases, affecting many cellular processes. Deregulation of the telomerase and the telomere complex leads to several biological disorders. We investigated the hypothesis that PCB153 modulates telomerase activity, telomeres and reactive oxygen species resulting in the deregulation of cell growth. Exponentially growing immortal human skin keratinocytes (HaCaT) and normal human foreskin keratinocytes (NFK) were incubated with PCB153 for 48 and 24. days, respectively, and telomerase activity, telomere length, superoxide level, cell growth, and cell cycle distribution were determined. In HaCaT cells exposure to PCB153 significantly reduced telomerase activity, telomere length, cell growth and increased intracellular superoxide levels from day 6 to day 48, suggesting that superoxide may be one of the factors regulating telomerase activity, telomere length and cell growth compared to untreated control cells. Results with NFK cells showed no shortening of telomere length but reduced cell growth and increased superoxide levels in PCB153-treated cells compared to untreated controls. As expected, basal levels of telomerase activity were almost undetectable, which made a quantitative comparison of treated and control groups impossible. The significant down regulation of telomerase activity and reduction of telomere length by PCB153 in HaCaT cells suggest that any cell type with significant telomerase activity, like stem cells, may be at risk of premature telomere shortening with potential adverse health effects for the affected organism.
机译:多氯联苯(PCBs)是普遍存在的环境污染物,其特征是环境中的长期持久性,生物积累和食物链中的生物放大作用。接触多氯联苯可能导致各种疾病,影响许多细胞过程。端粒酶和端粒复合体的失调导致几种生物学疾病。我们研究了PCB153调节端粒酶活性,端粒和活性氧导致细胞生长失调的假设。将指数增长的永生人类皮肤角质形成细胞(HaCaT)和正常人包皮角质形成细胞(NFK)与PCB153分别孵育48天和24天,并测定端粒酶活性,端粒长度,超氧化物水平,细胞生长和细胞周期分布。从第6天到第48天,暴露于PCB153中的HaCaT细胞会显着降低端粒酶活性,端粒长度,细胞生长并增加细胞内超氧化物水平,这表明与未处理的对照组相比,超氧化物可能是调节端粒酶活性,端粒长度和细胞生长的因素之一细胞。与未处理的对照组相比,NFK细胞的结果显示端粒长度没有缩短,但在经过PCB153处理的细胞中却减少了细胞的生长并增加了超氧化物水平。如预期的那样,基本无法检测到端粒酶活性的基础水平,这使得无法对治疗组和对照组进行定量比较。 HaCaT细胞中端粒酶活性的显着下调和PCB153导致端粒长度的减少表明,任何具有显着端粒酶活性的细胞类型(如干细胞)都可能处于端粒过早缩短的风险中,对受影响的生物体具有潜在的不利健康影响。

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