Department of Psychiatry, University of Geneva, Geneva, Switzerland.
Department of Basic Neuroscience, University of Geneva, Geneva, Switzerland.
Elife. 2018 Mar 20;7:e32017. doi: 10.7554/eLife.32017.
Delineating the basic cellular components of cortical inhibitory circuits remains a fundamental issue in order to understand their specific contributions to microcircuit function. It is still unclear how current classifications of cortical interneuron subtypes relate to biological processes such as their developmental specification. Here we identified the developmental trajectory of neurogliaform cells (NGCs), the main effectors of a powerful inhibitory motif recruited by long-range connections. Using in vivo genetic lineage-tracing in mice, we report that NGCs originate from a specific pool of 5-HTR-expressing cells located in the preoptic area (POA). -derived 5-HTR+ cortical interneurons (INs) expressed the transcription factors PROX1, NR2F2, the marker reelin but not VIP and exhibited the molecular, morphological and electrophysiological profile of NGCs. Overall, these results indicate that NGCs are a distinct class of INs with a unique developmental trajectory and open the possibility to study their specific functional contribution to cortical inhibitory microcircuit motifs.
为了理解皮质抑制性回路的特定贡献,阐明其基本细胞成分仍然是一个基本问题。目前的皮质中间神经元亚型分类与发育特化等生物学过程如何相关尚不清楚。在这里,我们确定了神经胶质形态细胞 (NGC) 的发育轨迹,NGC 是长程连接募集的强大抑制性基序的主要效应器。我们使用活体遗传谱系追踪在小鼠中报告说,NGC 起源于位于视前区 (POA) 的特定 5-HTR 表达细胞池。POA 衍生的 5-HTR+皮质中间神经元 (IN) 表达转录因子 PROX1、NR2F2、标志物 reelin,但不表达 VIP,并表现出 NGC 的分子、形态和电生理特征。总的来说,这些结果表明 NGC 是具有独特发育轨迹的独特 IN 类,为研究它们对皮质抑制性微回路基序的特定功能贡献开辟了可能性。