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顺行性突触特化过程中神经配体的体内纳米级图景

In vivo nanoscopic landscape of neurexin ligands underlying anterograde synapse specification.

作者信息

Nozawa Kazuya, Sogabe Taku, Hayashi Ayumi, Motohashi Junko, Miura Eriko, Arai Itaru, Yuzaki Michisuke

机构信息

Department of Physiology, Keio University School of Medicine, Tokyo 160-8582, Japan.

Department of Physiology, Keio University School of Medicine, Tokyo 160-8582, Japan.

出版信息

Neuron. 2022 Oct 5;110(19):3168-3185.e8. doi: 10.1016/j.neuron.2022.07.027. Epub 2022 Aug 24.

Abstract

Excitatory synapses are formed and matured by the cooperative actions of synaptic organizers, such as neurexins (Nrxns), neuroligins (Nlgns), LRRTMs, and Cbln1. Recent super-resolution nanoscopy developments have revealed that many synaptic organizers, as well as glutamate receptors and glutamate release machinery, exist as nanoclusters within synapses. However, it is unclear how such nanodomains interact with each other to organize excitatory synapses in vivo. By applying X10 expansion microscopy to epitope tag knockin mice, we found that Cbln1, Nlgn1, and LRRTM1, which share Nrxn as a common presynaptic receptor, form overlapping or separate nanodomains depending on Nrxn with or without a sequence encoded by splice site 4. The size and position of glutamate receptor nanodomains of GluD1, NMDA, and AMPA receptors were regulated by Cbln1, Nlgn1, and LRRTM1 nanodomains, respectively. These findings indicate that Nrxns anterogradely regulate the postsynaptic nanoscopic architecture of glutamate receptors through competition and coordination of Nrxn ligands.

摘要

兴奋性突触由突触组织者(如神经连接蛋白(Nrxns)、神经配蛋白(Nlgns)、富含亮氨酸重复跨膜蛋白(LRRTMs)和小脑蛋白1(Cbln1))的协同作用形成并成熟。最近超分辨率纳米显微镜技术的发展揭示,许多突触组织者以及谷氨酸受体和谷氨酸释放机制,在突触内以纳米簇的形式存在。然而,目前尚不清楚这些纳米结构域在体内如何相互作用以组织兴奋性突触。通过将X10扩展显微镜应用于表位标签敲入小鼠,我们发现,以Nrxn作为共同突触前受体的Cbln1、Nlgn1和LRRTM1,根据具有或不具有剪接位点4编码序列的Nrxn,形成重叠或分离的纳米结构域。GluD1、NMDA和AMPA受体的谷氨酸受体纳米结构域的大小和位置分别受Cbln1、Nlgn1和LRRTM1纳米结构域的调节。这些发现表明,Nrxns通过Nrxn配体的竞争和协调,顺行调节谷氨酸受体的突触后纳米结构。

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