首页> 外文期刊>Toxicology in vitro: an international journal published in association with BIBRA >Arsenic metabolites affect expression of the neurofilament and tau genes: an in-vitro study into the mechanism of arsenic neurotoxicity.
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Arsenic metabolites affect expression of the neurofilament and tau genes: an in-vitro study into the mechanism of arsenic neurotoxicity.

机译:砷代谢产物影响神经丝和tau基因的表达:对砷神经毒性机制的体外研究。

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摘要

Neurological studies indicate that the central (CNS) and peripheral nervous system (PNS) may be affected by arsenic (As). As-exposed patients show significantly lower nerve conduction velocities (NCVs) in their peripheral nerves in comparison to healthy subjects. As may play a role in the disruption of neuroskeletal integrity, but the mechanisms by which it exerts a toxic effect on the peripheral and central nervous system are still unclear. In the present study, we examined the neurotoxic effects of various arsenic metabolites (iAs(III), iAs(V), MMA(V) and DMA(V)) on two different cell lines derived from the peripheral (ST-8814) and central (SK-N-SH) nervous system. The effects of the arsenic metabolites were examined on the relative quantification levels of the cytoskeletal genes, neurofilament-light (NEFL), neurofilament-medium (NEF3), neurofilament-heavy (NEFH) and microtubule-associated protein-tau (MAPT), using real-time PCR. Our results show that iAs(III) and iAs(V) have no significant effects on either cell lines. On the other hand, MMA(V) and DMA(V) cause significant changes in expression levels of NEF3 and NEFL genes, while the expression level of the NEFH gene is significantly increased in both cell lines.
机译:神经学研究表明中枢(CNS)和周围神经系统(PNS)可能受砷(As)影响。与健康受试者相比,暴露后的患者在其周围神经中的神经传导速度(NCV)明显降低。可能在破坏神经骨骼完整性中发挥作用,但尚不清楚其对周围和中枢神经系统产生毒性作用的机制。在本研究中,我们研究了多种砷代谢物(iAs(III),iAs(V),MMA(V)和DMA(V))对两种源自外周血细胞(ST-8814)和中枢(SK-N-SH)神经系统。使用以下方法检查了砷代谢物对细胞骨架基因,神经丝轻(NEFL),神经丝中等(NEF3),神经丝重(NEFH)和微管相关蛋白τ(MAPT)相对定量水平的影响。实时PCR。我们的结果表明,iAs(III)和iAs(V)对两种细胞系均无明显影响。另一方面,MMA(V)和DMA(V)引起NEF3和NEFL基因表达水平的显着变化,而NEFH基因的表达水平在两种细胞系中均显着增加。

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