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发育中小鼠新皮层中 Ebf2-EGFP 表达的 Cajal-Retzius 细胞的形态和生理特征。

Morphological and Physiological Characteristics of Ebf2-EGFP-Expressing Cajal-Retzius Cells in Developing Mouse Neocortex.

机构信息

Institute of Biophysics, State Key Laboratory of Brain and Cognitive Sciences, CAS Center for Excellence in Brain Science and Intelligence Technology; Chinese Academy of Sciences, Beijing, China.

The College of Life Science, University of Chinese Academy of Sciences, Beijing, China.

出版信息

Cereb Cortex. 2019 Aug 14;29(9):3864-3878. doi: 10.1093/cercor/bhy265.

Abstract

Cajal-Retzius (CR) cells are one of the earliest populations of neurons in the cerebral cortex of rodents and primates, and they play a critical role in corticogenesis and cortical lamination during neocortical development. However, a comprehensive morphological and physiological profile of CR cells in the mouse neocortex has not yet been established. Here, we systematically investigated the dynamic development of CR cells in Tg(Ebf2-EGFP)58Gsat/Mmcd mice. The morphological complexity, membrane activities and presynaptic inputs of CR cells coordinately increase and reach a plateau at P5-P9 before regressing. Using 3D reconstruction, we delineated a parallel-stratification pattern of the axonal extension of CR cells. Furthermore, we found that the morphological structure and presynaptic inputs of CR cells were disturbed in Reelin-deficient mice. These findings confirm that CR cells undergo a transient maturation process in layer 1 before disappearing. Importantly, Reelin deficiency impairs the formation of synaptic connections onto CR cells. In conclusion, our results provide insights into the rapid maturation and axonal stratification of CR cells in layer 1. These findings suggest that both the electrophysiological activities and the morphology of CR cells provide vital guidance for the modulation of early circuits, in a Reelin-dependent manner.

摘要

Cajal-Retzius (CR) 细胞是啮齿动物和灵长类动物大脑皮层中最早出现的神经元群体之一,它们在新皮层发育过程中皮质发生和皮层分层中发挥着关键作用。然而,CR 细胞在小鼠新皮层中的全面形态和生理特征尚未建立。在这里,我们系统地研究了 Tg(Ebf2-EGFP)58Gsat/Mmcd 小鼠中 CR 细胞的动态发育。CR 细胞的形态复杂性、膜活性和突触前输入协同增加,并在 P5-P9 之前达到平台期,然后再退化。通过 3D 重建,我们描绘了 CR 细胞轴突延伸的平行分层模式。此外,我们发现 Reelin 缺陷型小鼠中 CR 细胞的形态结构和突触前输入受到干扰。这些发现证实了 CR 细胞在消失前在 1 层中经历了短暂的成熟过程。重要的是,Reelin 缺乏会损害 CR 细胞上突触连接的形成。总之,我们的研究结果为 CR 细胞在 1 层中的快速成熟和轴突分层提供了深入的了解。这些发现表明,CR 细胞的电生理活动和形态为早期回路的调节提供了重要的指导,这种调节方式依赖于 Reelin。

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