Baek Soonbong, Choi Hwan, Kim Jongpil
Department of Biomedical Engineering, Dongguk University, Seoul 100-715, Republic of Korea.
Department of Biomedical Engineering, Dongguk University, Seoul 100-715, Republic of Korea.
Brain Res. 2014 Oct 31;1587:23-32. doi: 10.1016/j.brainres.2014.08.059. Epub 2014 Sep 1.
The development of midbrain dopaminergic (DA) neurons is a complex process that requires the precise spatial and temporal expression of numerous genes. Here, we report that Ebf3, a transcription factor, plays a critical role in the terminal development of DA neurons. We found a specific upregulation of Ebf3 in Dicer knockout midbrain DA neurons and dynamic patterns of Ebf3 expression during the development of DA neurons. We further demonstrated that the overexpression of Ebf3 at the neural precursor stage of embryonic stem (ES) differentiation induces a significant increase in the number of TH+ DA neurons, whereas the suppression of Ebf3 leads to significant reduction in the development of TH+ DA neurons. Additionally, we found that Ebf3 is a candidate target for miR218 during DA neuronal development, such that the regulation of Ebf3 expression by miR218 controls the terminal differentiation of DA neurons. Thus, our data suggest that complex transcription factor-miRNA regulation is critical for the development of midbrain DA neurons.
中脑多巴胺能(DA)神经元的发育是一个复杂的过程,需要众多基因在精确的空间和时间上表达。在此,我们报告转录因子Ebf3在DA神经元的终末发育中起关键作用。我们发现Dicer基因敲除的中脑DA神经元中Ebf3有特异性上调,并且在DA神经元发育过程中Ebf3表达呈现动态模式。我们进一步证明,在胚胎干细胞(ES)分化的神经前体阶段过表达Ebf3会导致TH⁺ DA神经元数量显著增加,而抑制Ebf3则会导致TH⁺ DA神经元的发育显著减少。此外,我们发现Ebf3是DA神经元发育过程中miR218的候选靶标,因此miR218对Ebf3表达的调控控制着DA神经元的终末分化。因此,我们的数据表明复杂的转录因子 - miRNA调控对中脑DA神经元的发育至关重要。