Smirnova Lena, Block Katharina, Sittka Alexandra, Oelgeschläger Michael, Seiler Andrea E M, Luch Andreas
Federal Institute for Risk Assessment (BfR), Berlin, Germany.
PLoS One. 2014 Jun 4;9(6):e98892. doi: 10.1371/journal.pone.0098892. eCollection 2014.
Studying chemical disturbances during neural differentiation of murine embryonic stem cells (mESCs) has been established as an alternative in vitro testing approach for the identification of developmental neurotoxicants. miRNAs represent a class of small non-coding RNA molecules involved in the regulation of neural development and ESC differentiation and specification. Thus, neural differentiation of mESCs in vitro allows investigating the role of miRNAs in chemical-mediated developmental toxicity. We analyzed changes in miRNome and transcriptome during neural differentiation of mESCs exposed to the developmental neurotoxicant sodium valproate (VPA). A total of 110 miRNAs and 377 mRNAs were identified differently expressed in neurally differentiating mESCs upon VPA treatment. Based on miRNA profiling we observed that VPA shifts the lineage specification from neural to myogenic differentiation (upregulation of muscle-abundant miRNAs, mir-206, mir-133a and mir-10a, and downregulation of neural-specific mir-124a, mir-128 and mir-137). These findings were confirmed on the mRNA level and via immunochemistry. Particularly, the expression of myogenic regulatory factors (MRFs) as well as muscle-specific genes (Actc1, calponin, myosin light chain, asporin, decorin) were found elevated, while genes involved in neurogenesis (e.g. Otx1, 2, and Zic3, 4, 5) were repressed. These results were specific for valproate treatment and--based on the following two observations--most likely due to the inhibition of histone deacetylase (HDAC) activity: (i) we did not observe any induction of muscle-specific miRNAs in neurally differentiating mESCs exposed to the unrelated developmental neurotoxicant sodium arsenite; and (ii) the expression of muscle-abundant mir-206 and mir-10a was similarly increased in cells exposed to the structurally different HDAC inhibitor trichostatin A (TSA). Based on our results we conclude that miRNA expression profiling is a suitable molecular endpoint for developmental neurotoxicity. The observed lineage shift into myogenesis, where miRNAs may play an important role, could be one of the developmental neurotoxic mechanisms of VPA.
研究小鼠胚胎干细胞(mESCs)神经分化过程中的化学干扰,已被确立为一种用于识别发育性神经毒物的体外测试替代方法。微小RNA(miRNAs)是一类参与神经发育以及胚胎干细胞分化和特化调控的小非编码RNA分子。因此,mESCs的体外神经分化有助于研究miRNAs在化学介导的发育毒性中的作用。我们分析了暴露于发育性神经毒物丙戊酸钠(VPA)的mESCs神经分化过程中微小RNA组和转录组的变化。在VPA处理后,共鉴定出110种miRNAs和377种mRNA在神经分化的mESCs中差异表达。基于微小RNA分析,我们观察到VPA使谱系特化从神经分化转变为肌源性分化(肌肉丰富的miRNAs,即mir-206、mir-133a和mir-10a上调,而神经特异性的mir-124a、mir-128和mir-137下调)。这些发现通过mRNA水平和免疫化学得到了证实。特别地,发现肌源性调节因子(MRFs)以及肌肉特异性基因(Actc1、钙调蛋白、肌球蛋白轻链、骨桥蛋白、核心蛋白聚糖)的表达升高,而参与神经发生的基因(如Otx1、2以及Zic3、4、5)受到抑制。这些结果是丙戊酸盐处理所特有的,并且基于以下两点观察结果,很可能是由于组蛋白脱乙酰酶(HDAC)活性受到抑制:(i)在暴露于不相关的发育性神经毒物亚砷酸钠的神经分化mESCs中,我们未观察到任何肌肉特异性miRNAs的诱导;(ii)在暴露于结构不同的HDAC抑制剂曲古抑菌素A(TSA)的细胞中,肌肉丰富的mir-206和mir-10a的表达同样增加。基于我们的结果,我们得出结论,微小RNA表达谱分析是发育性神经毒性的一个合适分子终点。观察到的向肌生成的谱系转变,其中miRNAs可能起重要作用,可能是VPA的发育性神经毒性机制之一。