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轴突-轴突联系的分子机制。

Molecular mechanisms of axo-axonic innervation.

机构信息

INM, University of Monpellier, INSERM, CNRS, Monpellier, France.

Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, 11724, USA; Department of Neurobiology and Behavior, Stony Brook University, Stony Brook, NY, 11794, USA.

出版信息

Curr Opin Neurobiol. 2021 Aug;69:105-112. doi: 10.1016/j.conb.2021.03.002. Epub 2021 Apr 14.

Abstract

One of the most intriguing features of inhibitory synapses is the precision by which they innervate their target, not only at the cellular level but also at the subcellular level (i.e. axo-dendritic, axo-somatic, or axo-axonic innervation). In particular, in the cerebellum, cortex, and spinal cord, distinct and highly specialized GABAergic interneurons, such as basket cells, chandelier cells, and GABApre interneurons, form precise axo-axonic synapses, allowing them to directly regulate neuronal output and circuit function. In this article, we summarize our latest knowledge of the cellular and molecular mechanisms that regulate the establishment and maintenance of axo-axonic synapses in these regions of the CNS. We also detail the key roles of the L1CAM family of cell adhesion molecules in such GABAergic subcellular target recognition.

摘要

抑制性突触的一个最有趣的特征是它们精确地支配其靶标,不仅在细胞水平上,而且在亚细胞水平上(即轴突-树突、轴突-体、或轴突-轴突支配)。特别是在小脑、皮层和脊髓中,不同的、高度特化的 GABA 能中间神经元,如篮状细胞、钟形细胞和 GABA 能中间神经元,形成精确的轴突-轴突突触,使它们能够直接调节神经元的输出和电路功能。在本文中,我们总结了我们对调节中枢神经系统这些区域中轴突-轴突突触建立和维持的细胞和分子机制的最新认识。我们还详细描述了 L1CAM 细胞粘附分子家族在这种 GABA 能亚细胞靶标识别中的关键作用。

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