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海马神经元原代培养物中细胞储存区室的定位以及神经生长因子(NGF)组成型释放和活性依赖性释放的位点

Localization of cellular storage compartments and sites of constitutive and activity-dependent release of nerve growth factor (NGF) in primary cultures of hippocampal neurons.

作者信息

Blöchl A, Thoenen H

机构信息

Department of Neurochemistry, Max Planck Institute for Psychiatry, Martinsried, Germany.

出版信息

Mol Cell Neurosci. 1996 Mar;7(3):173-90. doi: 10.1006/mcne.1996.0014.

Abstract

The characteristics of the constitutive and activity-mediated secretion of NGF from native hippocampal slices are the same as those from hippocampal cultures transfected with an NGF-overexpressing plasmid (Blöchl and Thoenen, 1995). In these cultures, the distribution of intracellular NGF immunoreactivity-including the co-localization with endoplasmic reticulum (ER) and Golgi markers-in soma, dendrites, and axons, as visualized by confocal microscopy, is compatible with a localization of NGF in an ER-like compartment. Since the positively charged NGF molecule is bound, at the sites of its release, to the negatively charged neuronal surface, at low salt buffer concentrations, it was possible to attribute the different release mechanisms to specific neuronal surface sites. Constitutive secretion of NGF is confined to the neuronal soma and the very proximal parts of dendrites. In contrast, the activity-dependent secretion, initiated by high potassium or glutamate also occurs all along the neuronal processes, in particular dendrites. This release is independent of extracellular calcium, but depends on calcium released from intracellular calcium stores and is mediated by sodium influx via voltagegated sodium channels and non-NMDA glutamate receptors. The confocal intensity analysis of the NGF surface staining permitted quantitative assessment of the different release mechanisms to different neuronal domains.

摘要

来自天然海马切片的NGF组成型分泌和活性介导分泌的特征与用NGF过表达质粒转染的海马培养物中的特征相同(布洛赫尔和托嫩,1995年)。在这些培养物中,通过共聚焦显微镜观察到的细胞内NGF免疫反应性的分布——包括与内质网(ER)和高尔基体标记物的共定位——在胞体、树突和轴突中的情况,与NGF定位于内质网样区室的情况相符。由于带正电荷的NGF分子在其释放部位与带负电荷的神经元表面结合,在低盐缓冲液浓度下,有可能将不同的释放机制归因于特定的神经元表面位点。NGF的组成型分泌局限于神经元胞体和树突的非常近端部分。相比之下,由高钾或谷氨酸引发的活性依赖性分泌也沿着神经元突起,特别是树突发生。这种释放不依赖于细胞外钙,但依赖于从细胞内钙库释放的钙,并由通过电压门控钠通道和非NMDA谷氨酸受体的钠内流介导。对NGF表面染色的共聚焦强度分析允许对不同神经元区域的不同释放机制进行定量评估。

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