Reelin调节新生颗粒细胞树突棘的成熟、突触发生和胶质鞘的形成

Carles Bosch, Núria Masachs, David Exposito-Alonso, Albert Martı́nez, C. Teixeira, I. Fernaud, Lluís Pujadas, Fausto Ulloa, J. Comella, J. DeFelipe, Á. Merchán-Pérez, E. Soriano
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In contrast, 3D-electron microscopy (focused ion beam milling/scanning electron microscope) revealed that dysregulation of the Reelin/Dab1 pathway leads to both transient and permanent changes in the types and morphology of dendritic spines, mainly altering mushroom, filopodial, and branched GC spines. We also found that the Reelin/Dab1 pathway controls synaptic configuration of presynaptic boutons in the dentate gyrus, with its dysregulation leading to a substantial decrease in multi-synaptic bouton innervation. Lastly, we show that the Reelin/Dab1 pathway controls astroglial ensheathment of synapses. Thus, the Reelin pathway is a key regulator of adult-generated GC integration, by controlling dendritic spine types and shapes, their synaptic innervation patterns, and glial ensheathment. These findings may help to better understanding of hippocampal circuit alterations in neurological disorders in which the Reelin pathway is implicated. 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引用次数: 51

摘要

Reelin通路对神经迁移和突触连接的发育和成熟都是必不可少的。然而,其在成人突触形成和重塑中的作用仍在研究中。在这里,我们研究了Reelin/Dab1通路对年轻成年小鼠海马新生颗粒细胞(GCs)突触发生的影响。我们发现,无论是Reelin的过表达还是其细胞内适配器Dab1的失活,都不会实质性地改变这些神经元中的树突棘数。相反,3d电子显微镜(聚焦离子束铣削/扫描电镜)显示,Reelin/Dab1通路的失调导致树突棘的类型和形态发生短暂和永久的变化,主要改变蘑菇棘、丝状棘和分枝GC棘。我们还发现Reelin/Dab1通路控制齿状回突触前钮扣的突触构型,其失调导致多突触钮扣神经支配的显著减少。最后,我们发现Reelin/Dab1通路控制突触的星形胶质鞘。因此,Reelin通路通过控制树突棘的类型和形状、突触神经支配模式和胶质鞘,是成人生成的GC整合的关键调节因子。这些发现可能有助于更好地理解在牵涉到Reelin通路的神经系统疾病中海马回路的改变。细胞外蛋白Reelin在以海马回路为靶点的神经系统疾病,包括癫痫、阿尔茨海默病和精神疾病中具有重要作用。在这里,我们讨论了Reelin在成人生成的颗粒细胞(GCs)突触接触发育中的作用,GCs是一种对学习和记忆至关重要的神经元群体,与神经和精神疾病有关。我们发现Reelin通路控制树突棘的形状、大小和类型,多突触神经支配的复杂性以及控制突触内稳态的突触周围星形胶质鞘的程度。这些发现表明Reelin在GC突触发生中的关键作用,并为神经和精神疾病中可能发生的Reelin失调引起的结构电路改变提供了基础。
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Reelin Regulates the Maturation of Dendritic Spines, Synaptogenesis and Glial Ensheathment of Newborn Granule Cells
The Reelin pathway is essential for both neural migration and for the development and maturation of synaptic connections. However, its role in adult synaptic formation and remodeling is still being investigated. Here, we investigated the impact of the Reelin/Dab1 pathway on the synaptogenesis of newborn granule cells (GCs) in the young-adult mouse hippocampus. We show that neither Reelin overexpression nor the inactivation of its intracellular adapter, Dab1, substantially alters dendritic spine numbers in these neurons. In contrast, 3D-electron microscopy (focused ion beam milling/scanning electron microscope) revealed that dysregulation of the Reelin/Dab1 pathway leads to both transient and permanent changes in the types and morphology of dendritic spines, mainly altering mushroom, filopodial, and branched GC spines. We also found that the Reelin/Dab1 pathway controls synaptic configuration of presynaptic boutons in the dentate gyrus, with its dysregulation leading to a substantial decrease in multi-synaptic bouton innervation. Lastly, we show that the Reelin/Dab1 pathway controls astroglial ensheathment of synapses. Thus, the Reelin pathway is a key regulator of adult-generated GC integration, by controlling dendritic spine types and shapes, their synaptic innervation patterns, and glial ensheathment. These findings may help to better understanding of hippocampal circuit alterations in neurological disorders in which the Reelin pathway is implicated. Significance Statement The extracellular protein Reelin has an important role in neurological diseases, including epilepsy, Alzheimer's disease and psychiatric diseases, targeting hippocampal circuits. Here we address the role of Reelin in the development of synaptic contacts in adult-generated granule cells (GCs), a neuronal population that is crucial for learning and memory and implicated in neurological and psychiatric diseases. We found that the Reelin pathway controls the shapes, sizes, and types of dendritic spines, the complexity of multisynaptic innervations and the degree of the perisynaptic astroglial ensheathment that controls synaptic homeostasis. These findings show a pivotal role of Reelin in GC synaptogenesis and provide a foundation for structural circuit alterations caused by Reelin deregulation that may occur in neurological and psychiatric disorders.
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