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Folate Deficiency Induces Neural Stem Cell Apoptosis by Increasing Homocysteine In Vitro

机译:叶酸缺乏症通过增加同型半胱氨酸体外诱导神经干细胞凋亡。

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摘要

Cellular events for neural progenitor cells, such as proliferation and differentiation, are regulated by multiple intrinsic and extrinsic cell signals. Folate plays a central role in central nervous system development, so folate, as an extrinsic signal, may affect neural stem cell (NSC) proliferation and differentiation. In the present study, we investigated the effects of folate deficiency on the cell proliferation, cell apoptosis and homocysteine concentrations in NSCs. NSCs were isolated from fetal rats and identified as NSCs by their expression of immunoreactive nestin. Cell proliferation was quantitated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Apoptotic cells were detected and confirmed by flow cytometric analysis. We measured homocysteine concentrations in NSCs by high performance liquid chromatography and detected the expression of caspase-3 by western blot method. Folate deficiency not only decreased cell proliferation, but also increased the apoptotic rate of NSCs as demonstrated by the increased expression of early apoptotic markers such as caspase-3, compared to control group (p<0.05). Furthermore, There was a statistically significant increase in homocysteine concentration during folate deficiency in NSCs (p<0.05). These data suggest that folate affects the cell proliferation, apoptosis and homocysteine generation in NSC cells.
机译:神经祖细胞的细胞事件,例如增殖和分化,受到多种内在和外在细胞信号的调节。叶酸在中枢神经系统发育中起着核心作用,因此叶酸作为一种外在信号可能会影响神经干细胞(NSC)的增殖和分化。在本研究中,我们调查了叶酸缺乏对神经干细胞中细胞增殖,细胞凋亡和高半胱氨酸浓度的影响。从胎儿大鼠中分离出NSC,并通过表达免疫反应性巢蛋白将其鉴定为NSC。细胞增殖通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化物测定来定量。检测细胞凋亡并通过流式细胞术分析确认。我们通过高效液相色谱法测定了NSC中高半胱氨酸的浓度,并通过Western blot方法检测了caspase-3的表达。与对照组相比,叶酸缺乏不仅减少了细胞增殖,而且还增加了NSC的凋亡率,这由早期凋亡标记物(例如caspase-3)的表达增加所证明(p <0.05)。此外,在NSCs叶酸缺乏期间,同型半胱氨酸浓度在统计学上有显着增加(p <0.05)。这些数据表明叶酸影响NSC细胞中的细胞增殖,凋亡和同型半胱氨酸的产生。

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