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Differential Cytotoxic Effects of Titanium Oxide Nanoparticles on Peripheral Nervous System Neural Cells

机译:氧化钛纳米粒子对外周神经系统神经细胞的差异细胞毒性作用

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The health impact of exposure to TiO_2 nanoparticles is poorly understood. We recently found treatment with TiO_2 micro- or nanoparticles induce cell death in human astrocytes-like U87 astrocytoma cells and in normal human fibroblasts in a concentration-related manner. Because the cytotoxic effects of these nanoparticles in peripheral nervous system (PNS) neural cells have not been elucidated, we have developed two PNS neural cell models in vitro consisting of dorsal root ganglion (DRG) neurons and Schwann cells to facilitate the systematic investigation of such effects. We noted treatment with TiO_2 nanoparticles lowered the survival of both DRG neurons and Schwann cells in a dose- and time-related manner, DRG neurons being more sensitive than Schwann cells to the effects. Thus, our findings may have pathophysiological implications in the impact of exposure to TiO_2 nanoparticles on the structure and function of the PNS.
机译:暴露于TiO_2纳米颗粒的健康影响很难理解。我们最近发现用TiO_2微型或纳米颗粒治疗诱导人体星形胶质细胞样U87星形细胞瘤细胞的细胞死亡,并以浓度相关的方式在正常的人体成纤维细胞中。因为这些纳米颗粒在外周神经系统(PNS)神经细胞中的细胞毒性效应尚未阐明,我们已经开发了两种PNS神经细胞模型,其体外组成的背根神经节(DRG)神经元和施旺细胞,以促进对此的系统调查效果。我们注意到TiO_2纳米粒子的治疗以剂量和时间和时间的方式降低了DRG神经元和施旺细胞的存活,DRG神经元比Schwann细胞更敏感。因此,我们的发现可能具有在暴露于TiO_2纳米颗粒对PNS的结构和功能的影响下的病理生理学意义。

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