Ma Yan, Zhang Chen, Gao Xiao-Bo, Luo Hai-Yan, Chen Yang, Li Hui-hua, Ma Xu, Lu Cai-Ling
Graduate School of Peking Union Medical College, Beijing, China.
Department of Genetics, National Research Institute for Family Planning, Beijing, China.
Sci Rep. 2015 Nov 5;5:16093. doi: 10.1038/srep16093.
As a nutritional factor, folic acid can prevent cardiac and neural defects during embryo development. Our previous study showed that arsenic impairs embryo development by down-regulating Dvr1/GDF1 expression in zebrafish. Here, we investigated whether folic acid could protect against arsenic-mediated embryo toxicity. We found that folic acid supplementation increases hatching and survival rates, decreases malformation rate and ameliorates abnormal cardiac and neural development of zebrafish embryos exposed to arsenite. Both real-time PCR analysis and whole in-mount hybridization showed that folic acid significantly rescued the decrease in Dvr1 expression caused by arsenite. Subsequently, our data demonstrated that arsenite significantly decreased cell viability and GDF1 mRNA and protein levels in HEK293ET cells, while folic acid reversed these effects. Folic acid attenuated the increase in subcellular reactive oxygen species (ROS) levels and oxidative adaptor p66Shc protein expression in parallel with the changes in GDF1 expression and cell viability. P66Shc knockdown significantly inhibited the production of ROS and the down-regulation of GDF1 induced by arsenite. Our data demonstrated that folic acid supplementation protected against arsenic-mediated embryo toxicity by up-regulating the expression of Dvr1/GDF1, and folic acid enhanced the expression of GDF1 by decreasing p66Shc expression and subcellular ROS levels.
作为一种营养因子,叶酸可预防胚胎发育期间的心脏和神经缺陷。我们之前的研究表明,砷通过下调斑马鱼中的Dvr1/GDF1表达来损害胚胎发育。在此,我们研究了叶酸是否能预防砷介导的胚胎毒性。我们发现,补充叶酸可提高斑马鱼胚胎的孵化率和存活率,降低畸形率,并改善暴露于亚砷酸盐的斑马鱼胚胎的心脏和神经发育异常。实时PCR分析和全胚胎原位杂交均显示,叶酸显著挽救了由亚砷酸盐导致的Dvr1表达下降。随后,我们的数据表明,亚砷酸盐显著降低了HEK293ET细胞的细胞活力以及GDF1 mRNA和蛋白质水平,而叶酸则逆转了这些效应。叶酸减弱了亚细胞活性氧(ROS)水平的升高以及氧化衔接蛋白p66Shc的蛋白表达,这与GDF1表达和细胞活力的变化是平行的。敲低P66Shc可显著抑制由亚砷酸盐诱导的ROS生成以及GDF1的下调。我们的数据表明,补充叶酸通过上调Dvr1/GDF1的表达来预防砷介导的胚胎毒性,并且叶酸通过降低p66Shc表达和亚细胞ROS水平来增强GDF1的表达。