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星形胶质细胞通过Hevin桥接NRX1α和NL1来组装丘脑皮质突触。

Astrocytes Assemble Thalamocortical Synapses by Bridging NRX1α and NL1 via Hevin.

作者信息

Singh Sandeep K, Stogsdill Jeff A, Pulimood Nisha S, Dingsdale Hayley, Kim Yong Ho, Pilaz Louis-Jan, Kim Il Hwan, Manhaes Alex C, Rodrigues Wandilson S, Pamukcu Arin, Enustun Eray, Ertuz Zeynep, Scheiffele Peter, Soderling Scott H, Silver Debra L, Ji Ru-Rong, Medina Alexandre E, Eroglu Cagla

机构信息

Department of Cell Biology, Duke University Medical Center, Durham, NC 27710.

Department of Cell Biology, Duke University Medical Center, Durham, NC 27710.

出版信息

Cell. 2016 Jan 14;164(1-2):183-196. doi: 10.1016/j.cell.2015.11.034.

Abstract

Proper establishment of synapses is critical for constructing functional circuits. Interactions between presynaptic neurexins and postsynaptic neuroligins coordinate the formation of synaptic adhesions. An isoform code determines the direct interactions of neurexins and neuroligins across the synapse. However, whether extracellular linker proteins can expand such a code is unknown. Using a combination of in vitro and in vivo approaches, we found that hevin, an astrocyte-secreted synaptogenic protein, assembles glutamatergic synapses by bridging neurexin-1alpha and neuroligin-1B, two isoforms that do not interact with each other. Bridging of neurexin-1alpha and neuroligin-1B via hevin is critical for the formation and plasticity of thalamocortical connections in the developing visual cortex. These results show that astrocytes promote the formation of synapses by modulating neurexin/neuroligin adhesions through hevin secretion. Our findings also provide an important mechanistic insight into how mutations in these genes may lead to circuit dysfunction in diseases such as autism.

摘要

突触的正确建立对于构建功能回路至关重要。突触前神经配素与突触后神经连接蛋白之间的相互作用协调突触黏附的形成。一种异构体编码决定了神经配素和神经连接蛋白跨突触的直接相互作用。然而,细胞外连接蛋白是否能扩展这样的编码尚不清楚。通过结合体外和体内方法,我们发现硫酸乙酰肝素蛋白聚糖,一种星形胶质细胞分泌的促突触形成蛋白,通过桥接神经配素-1α和神经连接蛋白-1B来组装谷氨酸能突触,这两种异构体彼此不相互作用。通过硫酸乙酰肝素蛋白聚糖桥接神经配素-1α和神经连接蛋白-1B对于发育中的视觉皮层中丘脑皮质连接的形成和可塑性至关重要。这些结果表明,星形胶质细胞通过分泌硫酸乙酰肝素蛋白聚糖调节神经配素/神经连接蛋白黏附来促进突触形成。我们的发现还为这些基因的突变如何导致自闭症等疾病中的回路功能障碍提供了重要的机制性见解。

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