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大脑皮层发育过程中皮层迁移中的FLRTing神经元

FLRTing Neurons in Cortical Migration During Cerebral Cortex Development.

作者信息

Peregrina Claudia, Del Toro Daniel

机构信息

Department of Biological Sciences, Faculty of Medicine, Institute of Neurosciences, University of Barcelona, Barcelona, Spain.

Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.

出版信息

Front Cell Dev Biol. 2020 Sep 17;8:578506. doi: 10.3389/fcell.2020.578506. eCollection 2020.

Abstract

During development, two coordinated events shape the morphology of the mammalian cerebral cortex, leading to the cortex's columnar and layered structure: the proliferation of neuronal progenitors and cortical migration. Pyramidal neurons originating from germinal zones migrate along radial glial fibers to their final position in the cortical plate by both radial migration and tangential dispersion. These processes rely on the delicate balance of intercellular adhesive and repulsive signaling that takes place between neurons interacting with different substrates and guidance cues. Here, we focus on the function of the cell adhesion molecules fibronectin leucine-rich repeat transmembrane proteins (FLRTs) in regulating both the radial migration of neurons, as well as their tangential spread, and the impact these processes have on cortex morphogenesis. In combining structural and functional analysis, recent studies have begun to reveal how FLRT-mediated responses are precisely tuned - from forming different protein complexes to modulate either cell adhesion or repulsion in neurons. These approaches provide a deeper understanding of the context-dependent interactions of FLRTs with multiple receptors involved in axon guidance and synapse formation that contribute to finely regulated neuronal migration.

摘要

在发育过程中,两个协同事件塑造了哺乳动物大脑皮层的形态,形成了皮层的柱状和分层结构:神经元祖细胞的增殖和皮层迁移。源自生发区的锥体神经元通过径向迁移和切向扩散沿着径向胶质纤维迁移到它们在皮质板中的最终位置。这些过程依赖于在与不同底物和引导线索相互作用的神经元之间发生的细胞间粘附和排斥信号的微妙平衡。在这里,我们专注于富含亮氨酸重复序列跨膜蛋白纤连蛋白(FLRTs)在调节神经元的径向迁移及其切向扩散方面的功能,以及这些过程对皮层形态发生的影响。通过结合结构和功能分析,最近的研究开始揭示FLRT介导的反应是如何精确调节的——从形成不同的蛋白质复合物来调节神经元中的细胞粘附或排斥。这些方法提供了对FLRTs与参与轴突导向和突触形成的多种受体的上下文依赖性相互作用的更深入理解,这些相互作用有助于精细调节神经元迁移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7557/7527468/a5f443e1baf9/fcell-08-578506-g001.jpg

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