Institute of Anatomy and Cell Biology, Department of Molecular Embryology, Faculty of Medicine, University of Freiburg, Albertstrasse 17, D-79104, Freiburg, Germany.
Neuroanatomy, Faculty of Medicine, University of Freiburg, Albertstrasse 17, D-79104, Freiburg, Germany.
Cell Tissue Res. 2017 Nov;370(2):211-225. doi: 10.1007/s00441-017-2664-2. Epub 2017 Aug 11.
The temporal dynamic expression of Sonic Hedgehog (SHH) and signaling during early midbrain dopaminergic (mDA) neuron development is one of the key players in establishing mDA progenitor diversity. However, whether SHH signaling is also required during later developmental stages and in mature mDA neurons is less understood. We study the expression of SHH receptors Ptch1 and Gas1 (growth arrest-specific 1) and of the transcription factors Gli1, Gli2 and Gli3 in mouse midbrain during embryonic development [embryonic day (E) 12.5 onwards)], in newborn and adult mice using in situ hybridization and immunohistochemistry. Moreover, we examine the expression and regulation of dopaminergic neuronal progenitor markers, midbrain dopaminergic neuronal markers and markers of the SHH signaling pathway in undifferentiated and butyric acid-treated (differentiated) MN9D cells in the presence or absence of exogenous SHH in vitro by RT-PCR, immunoblotting and immunocytochemistry. Gli1 was expressed in the lateral mesencephalic domains, whereas Gli2 and Gli3 were expressed dorsolaterally and complemented by ventrolateral expression of Ptch1. Co-localization with tyrosine hydroxylase could not be observed. GAS1 was exclusively expressed in the dorsal mesencephalon at E11.5 and co-localized with Ki67. In contrast, MN9D cells expressed all the genes investigated and treatment of the cells with butyric acid significantly upregulated their expression. The results suggest that SHH is only indirectly involved in the differentiation and survival of mDA neurons and that the MN9D cell line is a valuable model for investigating early development but not the differentiation and survival of mDA neurons.
Sonic Hedgehog(SHH)的时空动态表达及其在早期中脑多巴胺能(mDA)神经元发育过程中的信号传导是建立 mDA 祖细胞多样性的关键因素之一。然而,SHH 信号传导在后期发育阶段和成熟的 mDA 神经元中是否也需要,目前了解较少。我们使用原位杂交和免疫组织化学技术,研究了 SHH 受体 Ptch1 和 Gas1(生长停滞特异性 1)以及转录因子 Gli1、Gli2 和 Gli3 在胚胎发育过程中(从胚胎第 12.5 天开始)、新生和成年小鼠的中脑中的表达。此外,我们还研究了多巴胺能神经元前体细胞标记物、中脑多巴胺能神经元标记物和 SHH 信号通路标记物在未分化和丁酸处理(分化)的 MN9D 细胞中的表达和调节,以及在存在或不存在外源 SHH 的情况下通过 RT-PCR、免疫印迹和免疫细胞化学进行体外研究。Gli1 在侧中脑区域表达,而 Gli2 和 Gli3 在背外侧表达,并与 Ptch1 的腹外侧表达互补。与酪氨酸羟化酶的共定位观察不到。GAS1 仅在 E11.5 时在背侧中脑表达,并与 Ki67 共定位。相比之下,MN9D 细胞表达了所有研究的基因,并且丁酸处理细胞显著上调了它们的表达。结果表明,SHH 仅间接参与 mDA 神经元的分化和存活,而 MN9D 细胞系是研究早期发育但不是 mDA 神经元的分化和存活的有价值模型。