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人类相关的持久性有机污染物(POPs)和全氟辛烷磺酸(PFOS)混合物增强了 PC12 细胞中神经生长因子(NGF)诱导的突起生长。

A human relevant mixture of persistent organic pollutants (POPs) and perfluorooctane sulfonic acid (PFOS) enhance nerve growth factor (NGF)-induced neurite outgrowth in PC12 cells.

机构信息

Department of Production Animal Clinical Sciences, Norwegian University of Life Sciences, P.O. Box 369 Sentrum, NO-0102, Oslo, Norway; Section for Pharmacology and Pharmaceutical Biosciences, Department of Pharmacy, University of Oslo, P.O. Box 1068, Blindern, NO-0316, Oslo, Norway.

Institute for Global Food Security, Queen's University Belfast, 19 Chlorine Gardens, Belfast, BT9 5DL, Northern Ireland, United Kingdom.

出版信息

Toxicol Lett. 2021 Mar 1;338:85-96. doi: 10.1016/j.toxlet.2020.12.007. Epub 2020 Dec 9.

Abstract

Disruption of neurite outgrowth is a marker for neurotoxicity. Persistent organic pollutants (POPs) are potential developmental neurotoxicants. We investigated their effect on neurite outgrowth in PC12 rat pheochromocytoma cells, in absence or presence of nerve growth factor (NGF), an inducer of neuronal differentiation. Cells were exposed for 72 h to a defined mixture of POPs with chemical composition and concentrations based on blood levels in the Scandinavian population. We also evaluated perfluorooctane sulfonic acid (PFOS) alone, the most abundant compound in the POP mixture. Only higher concentrations of POP mixture reduced tetrazolium salt (MTT) conversion. High-content analysis showed a decrease in cell number, but no changes for nuclear and mitochondrial cellular health parameters. Robust glutathione levels were observed in NGF-differentiated cells. Live imaging, using the IncuCyte ZOOM platform indicated ongoing cell proliferation over time, but slower in presence of NGF. The pollutants did not inhibit neuritogenesis, but rather increased NGF-induced neurite length. PFOS induced neurite outgrowth to about 50 % of the level seen with the POP mixture. Neither the POP mixture nor PFOS affected neurite length in the absence of NGF. Our observations indicate that realistic complex mixtures of environmental pollutants can affect neuronal connectivity via NGF-induced neurite outgrowth.

摘要

神经突生长的破坏是神经毒性的标志物。持久性有机污染物 (POPs) 是潜在的发育神经毒物。我们研究了它们在 PC12 大鼠嗜铬细胞瘤细胞中的神经突生长的影响,在有无神经生长因子 (NGF) 的情况下,NGF 是神经元分化的诱导剂。细胞在以斯堪的纳维亚人群血液水平为基础的化学组成和浓度的特定 POPs 混合物中暴露 72 小时。我们还单独评估了全氟辛烷磺酸 (PFOS),这是 POP 混合物中最丰富的化合物。只有较高浓度的 POP 混合物才会降低四唑盐 (MTT) 转化率。高内涵分析显示细胞数量减少,但核和线粒体细胞健康参数没有变化。在 NGF 分化的细胞中观察到强大的谷胱甘肽水平。使用 IncuCyte ZOOM 平台进行的实时成像表明,随着时间的推移,细胞增殖持续进行,但在 NGF 存在下增殖速度较慢。污染物不会抑制神经突生成,而是增加 NGF 诱导的神经突长度。PFOS 诱导的神经突生长达到与 POP 混合物相同水平的约 50%。在没有 NGF 的情况下,POP 混合物和 PFOS 均不影响神经突长度。我们的观察表明,现实复杂的环境污染物混合物可以通过 NGF 诱导的神经突生长影响神经元连接。

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