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三部分 NGL-1、netrin-G1 和 LAR 黏附复合物中的转导诱导顺式相互作用促进兴奋性突触的发育。

Trans-induced cis interaction in the tripartite NGL-1, netrin-G1 and LAR adhesion complex promotes development of excitatory synapses.

机构信息

Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 305-701, Korea.

出版信息

J Cell Sci. 2013 Nov 1;126(Pt 21):4926-38. doi: 10.1242/jcs.129718. Epub 2013 Aug 28.

Abstract

The initial contact between axons and dendrites at early neuronal synapses is mediated by surface adhesion molecules and is thought to induce synaptic maturation through the recruitment of additional synaptic proteins. The initiation of synaptic maturation should be tightly regulated to ensure that synaptic maturation occurs selectively at subcellular sites of axo-dendritic adhesion. However, the underlying mechanism is poorly understood. Here, we report that the initial trans-synaptic adhesion mediated by presynaptic netrin-G1 and postsynaptic NGL-1 (netrin-G1 ligand-1) induces a cis interaction between netrin-G1 and the receptor protein tyrosine phosphatase LAR (leukocyte antigen-related), and that this promotes presynaptic differentiation. We propose that trans-synaptic adhesions at early neuronal synapses trigger recruitment of neighboring adhesion molecules in a cis manner in order to couple initial axo-dendritic adhesion with synaptic differentiation.

摘要

早期神经元突触中轴突和树突之间的初始接触是由表面黏附分子介导的,通过募集更多的突触蛋白,诱导突触成熟。突触成熟的启动应该受到严格调控,以确保突触成熟选择性地发生在轴突-树突黏附的亚细胞部位。然而,其潜在机制尚不清楚。在这里,我们报告了由突触前 netrin-G1 和突触后 NGL-1(netrin-G1 配体-1)介导的初始跨突触黏附诱导 netrin-G1 与受体蛋白酪氨酸磷酸酶 LAR(白细胞相关抗原)之间的顺式相互作用,从而促进突触前分化。我们提出,早期神经元突触的跨突触黏附以顺式方式募集相邻的黏附分子,从而将初始的轴突-树突黏附与突触分化偶联起来。

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