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通过原子力显微镜和共聚焦显微镜对海马神经元上的 Met 受体进行纳米级成像。

Nanoscale mapping of the Met receptor on hippocampal neurons by AFM and confocal microscopy.

机构信息

Department of Veterinary and Comparative Anatomy, Pharmacology, and Physiology, Washington State University, Pullman, Washington, USA.

出版信息

Nanomedicine. 2013 Apr;9(3):428-38. doi: 10.1016/j.nano.2012.08.008. Epub 2012 Sep 7.

Abstract

UNLABELLED

Hepatocyte growth factor (HGF), a neurotrophic protein, acting through its tyrosine kinase receptor, Met, facilitates learning and synaptic plasticity. In concert with the role of the HGF/Met system in synaptic plasticity, we demonstrate that Met is localized to brain regions which undergo extensive synaptic remodeling. We demonstrate that Met activation results in an increase in dendritic spine density and functional synapses. Based on these observations, we hypothesized that Met should be associated with post-synaptic elements found on dendritic spines. Thus, the goal of this study was to determine the sub-cellular localization of Met on hippocampal neurons. Using an atomic force microscopy tip decorated with a specific Met antibody, the location of Met was mapped to different cellular compartments of hippocampal pyramidal neurons. Our results indicated that multimeric activated Met was found to be concentrated in the dendritic compartment while the inactivated monomeric form of Met was prominent on the soma.

FROM THE CLINICAL EDITOR

The goal of this study was to determine the sub-cellular localization of Met on hippocampal neurons using nanotechnology-based techniques, using an atomic force microscopy tip decorated with a specific Met antibody. The authors demonstrate that multimeric activated Met was found to be concentrated in the dendritic compartment while the inactivated monomeric form of Met was prominent in the soma of hippocampal pyramidal neurons.

摘要

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肝细胞生长因子(HGF)是一种神经营养蛋白,通过其酪氨酸激酶受体 Met 发挥作用,促进学习和突触可塑性。与 HGF/Met 系统在突触可塑性中的作用一致,我们证明 Met 定位于经历广泛突触重塑的脑区。我们证明 Met 的激活导致树突棘密度和功能性突触增加。基于这些观察结果,我们假设 Met 应该与树突棘上的突触后成分相关。因此,本研究的目的是确定 Met 在海马神经元上的亚细胞定位。使用原子力显微镜尖端修饰有特定 Met 抗体,将 Met 的位置映射到海马锥体神经元的不同细胞区室。我们的结果表明,多聚体激活的 Met 集中在树突区室中,而失活的单体形式的 Met 在体部突出。

临床编辑按

本研究旨在使用基于纳米技术的技术,使用原子力显微镜尖端修饰有特定 Met 抗体,确定 Met 在海马神经元上的亚细胞定位。作者证明,多聚体激活的 Met 集中在树突区室中,而失活的单体形式的 Met 在海马锥体神经元的体部突出。

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