Defteralı Çağla, Moreno-Estellés Mireia, Crespo Carlos, Díaz-Guerra Eva, Díaz-Moreno María, Vergaño-Vera Eva, Nieto-Estévez Vanesa, Hurtado-Chong Anahí, Consiglio Antonella, Mira Helena, Vicario Carlos
Instituto Cajal-Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain.
CIBERNED-Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Stem Cells. 2021 Sep;39(9):1253-1269. doi: 10.1002/stem.3393. Epub 2021 May 17.
Although previous studies suggest that neural stem cells (NSCs) exist in the adult olfactory bulb (OB), their location, identity, and capacity to generate mature neurons in vivo has been little explored. Here, we injected enhanced green fluorescent protein (EGFP)-expressing retroviral particles into the OB core of adult mice to label dividing cells and to track the differentiation/maturation of any neurons they might generate. EGFP-labeled cells initially expressed adult NSC markers on days 1 to 3 postinjection (dpi), including Nestin, GLAST, Sox2, Prominin-1, and GFAP. EGFP -doublecortin (DCX) cells with a migratory morphology were also detected and their abundance increased over a 7-day period. Furthermore, EGFP-labeled cells progressively became NeuN neurons, they acquired neuronal morphologies, and they became immunoreactive for OB neuron subtype markers, the most abundant representing calretinin expressing interneurons. OB-NSCs also generated glial cells, suggesting they could be multipotent in vivo. Significantly, the newly generated neurons established and received synaptic contacts, and they expressed presynaptic proteins and the transcription factor pCREB. By contrast, when the retroviral particles were injected into the subventricular zone (SVZ), nearly all (98%) EGFP -cells were postmitotic when they reached the OB core, implying that the vast majority of proliferating cells present in the OB are not derived from the SVZ. Furthermore, we detected slowly dividing label-retaining cells in this region that could correspond to the population of resident NSCs. This is the first time NSCs located in the adult OB core have been shown to generate neurons that incorporate into OB circuits in vivo.
尽管先前的研究表明成年嗅球(OB)中存在神经干细胞(NSC),但其在体内的位置、特性以及生成成熟神经元的能力却鲜有探索。在此,我们将表达增强型绿色荧光蛋白(EGFP)的逆转录病毒颗粒注射到成年小鼠的嗅球核心,以标记分裂细胞并追踪它们可能生成的任何神经元的分化/成熟过程。注射后第1至3天(dpi),EGFP标记的细胞最初表达成年神经干细胞标志物,包括巢蛋白、谷氨酸转运体1、性别决定区Y框蛋白2、多能干细胞标记蛋白1和胶质纤维酸性蛋白。还检测到具有迁移形态的EGFP -双皮质素(DCX)细胞,其数量在7天内增加。此外,EGFP标记的细胞逐渐变成NeuN神经元,获得神经元形态,并对嗅球神经元亚型标志物产生免疫反应,其中最丰富的是表达钙视网膜蛋白的中间神经元。嗅球神经干细胞还生成了神经胶质细胞,表明它们在体内可能具有多能性。值得注意的是,新生成的神经元建立并接受了突触联系,并且它们表达突触前蛋白和转录因子磷酸化环磷腺苷反应元件结合蛋白。相比之下,当将逆转录病毒颗粒注射到脑室下区(SVZ)时,几乎所有(98%)到达嗅球核心的EGFP -细胞都已停止有丝分裂,这意味着嗅球中绝大多数增殖细胞并非源自脑室下区。此外,我们在该区域检测到缓慢分裂的标记保留细胞,它们可能与驻留神经干细胞群体相对应。这是首次表明位于成年嗅球核心的神经干细胞能够在体内生成整合到嗅球回路中的神经元。