State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, 100085, China.
University of Chinese Academy of Sciences, Beijing, 100085, China.
Sci Rep. 2017 Aug 31;7(1):10103. doi: 10.1038/s41598-017-10311-3.
Emerging evidence has shown that dioxin causes dysregulation of microRNAs (miRs) in a variety of tissues or cells. However, little is known about dioxin effects on neuronal miRs expression. In the present study, 277 differentially expressed miRs were identified by miRs microarray analysis in 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD, at 10 M) treated SK-N-SH neuroblastoma cells. Among them, 53 miRs exhibited changes of more than 0.4-fold. Consistent with the microarray data, we verified the induction effect of TCDD on hsa-miR-608 expression, which is a primate-specific miR associated with brain functions. Bioinformatics analysis showed involvement of hsa-miR-608 in cytoskeleton organization, in which one of the hsa-miR-608 target genes, Cell Division Cycle 42 (CDC42), might play a role. We also confirmed induction of CDC42 expression by TCDD in SK-N-SH cells. TCDD induced the expression of CDC42 mRNA in hsa-miR-608 inhibitor transfected cells more obviously than in control cells, suggesting involvement of both transcriptional and post-transcriptional mechanisms in the TCDD-induced CDC42 regulation. Furthermore, CH223191, an antagonist of the aryl hydrocarbon receptor (AhR), counteracted TCDD-induced hsa-miR-608 and CDC42 expression. These results indicated that AhR not only mediates transcriptional induction of CDC42, but also hsa-miR-608-induced post-transcriptional regulation of CDC42 in dioxin treated neuroblastoma cells.
新兴证据表明,二恶英会导致多种组织或细胞中的 microRNAs(miRs)失调。然而,人们对二恶英对神经元 miR 表达的影响知之甚少。在本研究中,通过 2,3,7,8-四氯二苯并对二恶英(TCDD,10 μM)处理的 SK-N-SH 神经母细胞瘤细胞中的 miR 微阵列分析鉴定出 277 个差异表达的 miR。其中,53 个 miR 的变化超过 0.4 倍。与微阵列数据一致,我们验证了 TCDD 对 hsa-miR-608 表达的诱导作用,hsa-miR-608 是一种与大脑功能相关的灵长类特异性 miR。生物信息学分析表明 hsa-miR-608 参与细胞骨架组织,其中 hsa-miR-608 的一个靶基因 Cell Division Cycle 42(CDC42)可能发挥作用。我们还证实了 TCDD 在 SK-N-SH 细胞中诱导 CDC42 表达。TCDD 在 hsa-miR-608 抑制剂转染细胞中诱导的 CDC42 表达比对照细胞更明显,这表明 TCDD 诱导的 CDC42 调节涉及转录和转录后机制。此外,芳基烃受体(AhR)拮抗剂 CH223191 拮抗了 TCDD 诱导的 hsa-miR-608 和 CDC42 表达。这些结果表明,AhR 不仅介导了 CDC42 的转录诱导,还介导了 TCDD 处理的神经母细胞瘤细胞中 hsa-miR-608 诱导的 CDC42 转录后调节。