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抗体定向细胞外邻近生物素化揭示了 Contactin-1 调节轴突起始段的轴突-轴突神经支配。

Antibody-directed extracellular proximity biotinylation reveals that Contactin-1 regulates axo-axonic innervation of axon initial segments.

机构信息

Department of Neuroscience, Baylor College of Medicine, Houston, TX, USA.

Division of Neuroscience, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, USA.

出版信息

Nat Commun. 2023 Oct 26;14(1):6797. doi: 10.1038/s41467-023-42273-8.

Abstract

Axon initial segment (AIS) cell surface proteins mediate key biological processes in neurons including action potential initiation and axo-axonic synapse formation. However, few AIS cell surface proteins have been identified. Here, we use antibody-directed proximity biotinylation to define the cell surface proteins in close proximity to the AIS cell adhesion molecule Neurofascin. To determine the distributions of the identified proteins, we use CRISPR-mediated genome editing for insertion of epitope tags in the endogenous proteins. We identify Contactin-1 (Cntn1) as an AIS cell surface protein. Cntn1 is enriched at the AIS through interactions with Neurofascin and NrCAM. We further show that Cntn1 contributes to assembly of the AIS extracellular matrix, and regulates AIS axo-axonic innervation by inhibitory basket cells in the cerebellum and inhibitory chandelier cells in the cortex.

摘要

轴突起始段(AIS)细胞膜蛋白在神经元中介导关键的生物学过程,包括动作电位起始和轴突-轴突突触形成。然而,只有少数 AIS 细胞膜蛋白被鉴定出来。在这里,我们使用抗体导向的邻近生物素化来定义与 AIS 细胞黏附分子神经束蛋白(Neurofascin)接近的细胞膜蛋白。为了确定鉴定出的蛋白的分布,我们使用 CRISPR 介导的基因组编辑在内源性蛋白中插入表位标签。我们确定接触蛋白 1(Cntn1)为 AIS 细胞膜蛋白。Cntn1 通过与神经束蛋白和 NrCAM 的相互作用在 AIS 处富集。我们进一步表明 Cntn1 有助于 AIS 细胞外基质的组装,并通过小脑的抑制性篮状细胞和皮质的抑制性钟形细胞调节 AIS 的轴突-轴突神经支配。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a664/10603070/b79f890ed2cd/41467_2023_42273_Fig1_HTML.jpg

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