Fernández Acosta Francisco J, Luque-Molina Inma, Vecino Rebeca, Díaz-Guerra Eva, Defterali Çagla, Pignatelli Jaime, Vicario Carlos
Instituto Cajal (IC), CSIC, Madrid, Spain.
Centro de Investigación Biomédica en Red Sobre Enfermedades Neurodegenerativas (CIBERNED), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Front Cell Dev Biol. 2022 Jun 29;10:932297. doi: 10.3389/fcell.2022.932297. eCollection 2022.
Neural stem cells (NSCs) in the olfactory bulb (OB) core can generate mature interneurons in the adult mice brain. The vast majority of these adult generated cells express the calcium-binding protein Calretinin (CalR), and they migrate towards different OB layers. However, these cells have yet to be fully characterized and hence, to achieve this we injected retroviral particles expressing GFP into the OB core of adult animals and found that the CalR neurons generated from NSCs mainly migrate to the granule cell layer (GCL) and glomerular layer (GL) in similar proportions. In addition, since morphology and function are closely related, we used three-dimensional imaging techniques to analyze the morphology of these adult born cells, describing new subtypes of CalR interneurons based on their dendritic arborizations and projections, as well as their localization in the GCL or GL. We also show that the migration and morphology of these newly generated neurons can be altered by misexpressing the transcription factor Tbr1 in the OB core. Therefore, the morphology acquired by neurons located in a specific OB layer is the result of a combination of both extrinsic (e.g., layer allocation) and intrinsic mechanisms (e.g., transcription factors). Defining the cellular processes and molecular mechanisms that govern adult neurogenesis might help better understand brain circuit formation and plasticity, as well as eventually opening the way to develop strategies for brain repair.
嗅球(OB)核心区域的神经干细胞(NSCs)能够在成年小鼠大脑中生成成熟的中间神经元。这些成年后生成的细胞绝大多数表达钙结合蛋白钙视网膜蛋白(CalR),并且它们会向OB的不同层迁移。然而,这些细胞尚未得到充分表征,因此,为了实现这一点,我们将表达绿色荧光蛋白(GFP)的逆转录病毒颗粒注射到成年动物的OB核心区域,发现由神经干细胞产生的CalR神经元主要以相似的比例迁移到颗粒细胞层(GCL)和肾小球层(GL)。此外,由于形态与功能密切相关,我们使用三维成像技术分析这些成年后生成细胞的形态,根据它们树突分支和投射以及在GCL或GL中的定位来描述CalR中间神经元的新亚型。我们还表明,通过在OB核心区域错误表达转录因子Tbr1,可以改变这些新生成神经元的迁移和形态。因此,位于特定OB层的神经元所获得的形态是外在机制(如层分配)和内在机制(如转录因子)共同作用的结果。确定控制成年神经发生的细胞过程和分子机制可能有助于更好地理解脑回路的形成和可塑性,并最终为开发脑修复策略开辟道路。