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High Vulnerability of Oligodendrocytes to Oxidative Stress Induced by Ultrafine Urban Particles

机译:少突胶质细胞的高脆性对超细城市粒子引起的氧化应激

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摘要

Oligodendrocytes, myelin-forming cells in the brain, are vulnerable to oxidative stress. Recent work indicates that air pollution causes demyelinating diseases such as multiple sclerosis. However, little is known about the mechanism of toxicity of ultrafine particulate matters (PMs) to oligodendrocytes. Here, we aimed to determine whether oligodendrocyte precursor cells (OPCs) and mature oligodendrocytes (mOLs) are more vulnerable to ultrafine urban PMs (uf-UPs) than other types of brain cells and damage to adult OPCs and mOLs in the mouse brain exposed to uf-UPs. For in vitro experiments, following exposure to various concentrations (2, 20, and 200 μg/mL) of uf-UPs, we measured survival rates, the amount of reactive oxygen species (ROS), and the total antioxidant capacities (TACs) of brain cells isolated from neonatal Sprague-Dawley rats. For animal experiments, after a four-week exposure to a uf-UP suspension (20 μL, 0.4 mg/mL), we enumerated the number of damaged cells and typed damaged cells in the white matter of the cerebellum of uf-UP-exposed mice. MTT assays and Hoechst staining demonstrated that OPCs and mOLs were more vulnerable to uf-UP-induced damage than astrocytes and cortical neurons at 2, 20, and 200 μg/mL of uf-UPs examined in this study (p < 0.05). Damage to OPCs and mOLs depended on uf-UP concentration. DCF assays and DHE staining indicated that the amount of ROS generated in OPCs and mOLs was significantly higher than in other brain cell types (p < 0.05). In contrast, TAC values in OPCs and mOLs were significantly lower than those of other brain cell types (p < 0.05). Fluoro-Jade B (FJB)-positive cells in the cerebellar white matter of the uf-UP-exposed group were significantly greater in number relative to the control group. Double immunofluorescence indicated that FJB-positive cells are NG2-positive adult OPCs and carbon anhydrase II-positive mOLs. Taken together, our findings suggest that oxidative stress induced by uf-UPs in the brain impairs adult OPCs and mOLs, causing demyelination and reducing the capacity for remyelination.
机译:少突胶质细胞,大脑中形成髓鞘的细胞,易于氧化应激。最近的工作表明,空气污染导致脱髓鞘等脱髓鞘等疾病。然而,关于超细颗粒物质物质(PMS)至oligodendrocytes的毒性机制很少。在这里,我们旨在确定少突胶质细胞前体细胞(OPCs)和成熟的少突胚细胞(摩尔)比其他类型的脑细胞更容易受到超细城市PMS(UF-UPS),以及在暴露于的小鼠脑中对成人OPCS和摩尔人的损害UF-UPS。对于在体外实验中,在暴露于各种浓度(2,20和200μg/ mL)的UF-UPS之后,我们测量了存活率,活性氧物质(ROS)的量,以及总抗氧化能力(TAC)从新生儿sprague-dawley大鼠分离的脑细胞。对于动物实验,经过四周暴露于UF-up悬浮液(20μL,0.4mg / ml)后,我们列举了受损细胞的数量,并在UF-Up-曝光的白蚁中键入受损细胞老鼠。 MTT测定和Hoechst染色证明,OPCs和摩尔斯比在本研究中检查的2,20和200μg/ ml的UF-UPS的星形胶质细胞和皮质神经元更容易受UF-Up诱导的损伤(P <0.05)。 OPCS和MOL损坏依赖于UF-UP浓度。 DCF测定和DHE染色表明,OPCS和摩尔中产生的RO的量显着高于其他脑细胞类型(P <0.05)。相反,OPCs和摩尔中的TAC值显着低于其他脑细胞类型(P <0.05)。在相对于对照组的数量中,UF-Up曝光组小脑白质中的氟代玉氏B(FJB) - 阳性细胞显着更大。双免疫荧光表明FJB阳性细胞是NG2阳性的成分OPCs和碳酸酐酶II阳性摩尔。我们的研究结果表明,UF-UPS在脑中诱导的氧化应激损害成分OPCs和摩尔,引起脱髓鞘并降低雷米髓鞘的能力。

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