Casciano Fabio, Bianchi Nicoletta, Borin Mirta, Vellani Vittorio, Secchiero Paola, Bergamini Carlo M, Capsoni Simona, Pignatelli Angela
Department of Translational Medicine and LTTA Centre, University of Ferrara, 44121 Ferrara, Italy.
Interdepartmental Research Center for the Study of Multiple Sclerosis and Inflammatory and Degenerative Diseases of the Nervous System, University of Ferrara, 44121 Ferrara, Italy.
Biology (Basel). 2023 Feb 25;12(3):367. doi: 10.3390/biology12030367.
The olfactory bulb (OB) is one of two regions of the mammalian brain which undergo continuous neuronal replacement during adulthood. A significant fraction of the cells added in adulthood to the bulbar circuitry is constituted by dopaminergic (DA) neurons. We took advantage of a peculiar property of dopaminergic neurons in transgenic mice expressing eGFP under the tyrosine hydroxylase (TH) promoter: while DA neurons located in the glomerular layer (GL) display full electrophysiological maturation, eGFP+ cells in the mitral layer (ML) show characteristics of immature cells. In addition, they also display a lower fluorescence intensity, possibly reflecting different degrees of maturation. To investigate whether this difference in maturation might be confirmed at the gene expression level, we used a fluorescence-activated cell sorting technique on enzymatically dissociated cells of the OB. The cells were divided into two groups based on their level of fluorescence, possibly corresponding to immature ML cells and fully mature DA neurons from the GL. Semiquantitative real-time PCR was performed to detect the level of expression of genes linked to the degree of maturation of DA neurons. We showed that indeed the cells expressing low eGFP fluorescence are immature neurons. Our method can be further used to explore the differences between these two groups of DA neurons.
嗅球(OB)是成年哺乳动物大脑中两个经历持续神经元替代的区域之一。成年期添加到嗅球回路中的细胞有很大一部分是由多巴胺能(DA)神经元构成的。我们利用了在酪氨酸羟化酶(TH)启动子控制下表达增强绿色荧光蛋白(eGFP)的转基因小鼠中多巴胺能神经元的一个特殊特性:位于肾小球层(GL)的DA神经元显示出完全的电生理成熟,而二尖瓣层(ML)中的eGFP+细胞表现出未成熟细胞的特征。此外,它们还显示出较低的荧光强度,这可能反映了不同程度的成熟。为了研究这种成熟度的差异是否在基因表达水平上得到证实,我们对酶解的嗅球细胞使用了荧光激活细胞分选技术。根据细胞的荧光水平将其分为两组,可能分别对应于来自ML的未成熟细胞和来自GL的完全成熟的DA神经元。进行半定量实时PCR以检测与DA神经元成熟度相关的基因表达水平。我们表明,确实表达低eGFP荧光的细胞是未成熟神经元。我们的方法可进一步用于探索这两组DA神经元之间的差异。