Rostami Ali Akbar, Mohseni Kouchesfahani Homa, Kiani Sahar, Fakheri Rahman
Department of Animal Biology, Faculty of Biological Science, Kharazmi University, Tehran, Iran.
Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
Arch Iran Med. 2015 Sep;18(9):586-90.
In recent years the increasing use of nanoparticles has led researchers to study their effects on biological systems. The most important effects of nanoparticles on cells are their ability to induce or suppress production of reactive oxygen species (ROS). Changes in reactive oxygen species play an important role in various developmental processes, including proliferation and differentiation in several diseases such as Parkinson. The aim of this study was to investigate the effect of iron oxide nanoparticle with dimensions of less than 20 nanometers on the viability and neuronal differentiation of mouse embryonic stem cell (Royan B1).
To assess the effects of Fe2O3 nanoparticles on neuronal differentiation of Royan B1 cells, embryoid bodies were divided into eight groups receiving different amounts of nanoparticle (10, 20, 30 μg/mL) for 12 hours, retinoic acid (1 μM), and both. Differentiation was examined under phase contrast microscope and using immunocytochemistry.
Data analysis showed that cell death was increased by a time and concentration manner and there was a direct relevance between iron oxide amount and H2O2 level in cells. Statistical analysis of embryoid bodies showed that neural differentiation of mouse embryonic stem cells in groups that received nanoparticles were significantly lower than other groups and their viability were considerably reduced.
According to the findings of this study it can be concluded that iron oxide nanoparticles reduce retinoic acid-neuronal differentiation in mouse embryonic stem cells and it seems that the main mechanism involved in the reduction of viability and neural differentiation was enhanced levels of ROS within the cells.
近年来,纳米颗粒的使用日益增加,这促使研究人员研究其对生物系统的影响。纳米颗粒对细胞最重要的影响是它们诱导或抑制活性氧(ROS)产生的能力。活性氧的变化在各种发育过程中发挥着重要作用,包括帕金森病等几种疾病中的增殖和分化。本研究的目的是调查尺寸小于20纳米的氧化铁纳米颗粒对小鼠胚胎干细胞(Royan B1)活力和神经元分化的影响。
为了评估Fe2O3纳米颗粒对Royan B1细胞神经元分化的影响,将胚状体分为八组,分别接受不同量的纳米颗粒(10、20、30μg/mL)处理12小时、视黄酸(1μM)处理以及两者同时处理。在相差显微镜下并使用免疫细胞化学方法检查分化情况。
数据分析表明,细胞死亡以时间和浓度依赖的方式增加,并且细胞内氧化铁含量与H2O2水平之间存在直接相关性。胚状体的统计分析表明,接受纳米颗粒处理的组中小鼠胚胎干细胞的神经分化明显低于其他组,并且它们的活力显著降低。
根据本研究的结果可以得出结论,氧化铁纳米颗粒会降低小鼠胚胎干细胞中视黄酸诱导的神经元分化,并且似乎细胞内活性氧水平升高是导致活力和神经分化降低的主要机制。