Department of Physiology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan.
Mol Brain. 2010 Feb 2;3:5. doi: 10.1186/1756-6606-3-5.
The molecular mechanisms governing the differentiation of neural stem cells (NSCs) into neuronal progenitor cells and finally into neurons are gradually being revealed. The lack of convenient means for real-time determination of the stages of differentiation of individual neural cells, however, has been hindering progress in elucidating the mechanisms. In order to be able to easily identify the stages of differentiation of neural cells, we have been attempting to establish a mouse system that would allow progression of neuronal differentiation to be visualized based on transitions between fluorescence colors by using a combination of mouse genetics and the ever-expanding repertoire of fluorescent proteins. In this study we report the initial version of such a mouse system, which we call "Color Timer." We first generated transgenic (Tg; nestin/KOr Tg) mice in which production of the fluorescent protein Kusabira-Orange (KOr) is controlled by the gene regulatory elements within the 2nd intronic enhancer of the nestin gene, which is a good marker for NSCs, so that NSCs would emit orange fluorescence upon excitation. We then confirmed by immunohistochemical and immunocytochemical analyses that the KOr fluorescence closely reflected the presence of the Nestin protein. We also confirmed by a neurosphere formation assay that the intensity of the KOr fluorescence correlated with "stemness" of the cell and it was possible to readily identify NSCs in the two neurogenic regions, namely the dentate gyrus of the hippocampus and the subventricular zone of the lateral ventricle, in the brain of adult nestin/KOr Tg mice by the orange fluorescence they emitted. We then crossed nestin/KOr mice with doublecortin-enhanced Green Fluorescent Protein Tg mice, whose immature neurons emit green fluorescence upon excitation, and it was possible to visualize the progress of NSC-to-neuron differentiation by the transition between fluorescence colors from orange to green. This two-color initial version of the "Color Timer" mouse system will provide a powerful new tool for neurogenesis research.
神经干细胞(NSCs)向神经元祖细胞分化,最终分化为神经元的分子机制正逐渐被揭示。然而,缺乏实时确定单个神经细胞分化阶段的便捷手段,一直阻碍着对这些机制的阐明。为了能够轻松识别神经细胞的分化阶段,我们一直在尝试建立一种小鼠系统,该系统可利用小鼠遗传学和不断扩展的荧光蛋白库,通过荧光颜色的转换,可视化神经元分化的进展。在这项研究中,我们报告了这种小鼠系统的初始版本,我们称之为“Color Timer”。我们首先生成了转(Tg)基因鼠(nestin/KOr Tg),其中荧光蛋白 Kusabira-Orange(KOr)的产生受 nestin 基因第 2 内含子增强子内的基因调控元件的控制,nestin 是 NSCs 的良好标志物,因此 NSCs 在激发时会发出橙色荧光。然后,我们通过免疫组织化学和免疫细胞化学分析证实,KOr 荧光密切反映了 Nestin 蛋白的存在。我们还通过神经球形成测定证实,KOr 荧光的强度与细胞的“干性”相关,并且可以通过发出的橙色荧光,很容易在成年 nestin/KOr Tg 小鼠的大脑中两个神经发生区域(海马齿状回和侧脑室下区)中识别 NSCs。然后,我们将 nestin/KOr 小鼠与双皮质素增强型绿色荧光蛋白 Tg 小鼠(其不成熟神经元在激发时发出绿色荧光)杂交,并通过荧光颜色从橙色到绿色的转变,可视化 NSC 向神经元分化的进展。这种“Color Timer”小鼠系统的双色初始版本将为神经发生研究提供一种强大的新工具。