Suppr超能文献

新生大鼠前脑神经元生长锥的分离与部分特性研究

Isolation and partial characterisation of neuronal growth cones from neonatal rat forebrain.

作者信息

Gordon-Weeks P R, Lockerbie R O

出版信息

Neuroscience. 1984 Sep;13(1):119-36. doi: 10.1016/0306-4522(84)90264-1.

Abstract

We have devised a method for the isolation of viable neuronal growth cones from neonatal rat forebrain. The method involves differential and density gradient centrifugation and exploits the relatively low buoyant density (approximately 1.018 g/cm3) of growth cones. There are no known biochemical markers for growth cones and it was necessary therefore to monitor for their presence during the isolation using transmission electron microscopy. Several criteria were used to identify isolated growth cones including the presence of filopodia, an extensive system of branching, tubular smooth endoplasmic reticulum and a region rich in microfilaments subjacent to the plasma membrane. These morphological features are similar to those of growth cones identified unequivocally in intact developing brain and in tissue culture. Electron microscopical analysis showed that greater than 90% of membrane-bound, identifiable objects in one fraction were growth cones by these criteria. The major contaminant consisted of membrane sacs and vesicles of unidentified origin. There were only small amounts of isolated rough endoplasmic reticulum and mitochondria. Isolated growth cones were roughly spherical in shape with a diameter of 1.9 +/- 0.5 micron (mean +/- 1 SD). They usually contained mitochondria, large granular vesicles and small vesicles, and occasionally contained coated vesicles, lysosomes, lamellar bodies and multivesicular bodies, and only very rarely, intermediate filaments. Occasionally, growth cones had rudimentary synapses on them. The viability of isolated growth cones was investigated by observing their behaviour in short-term culture. After a few hours in culture on poly-D-lysine-coated coverslips, growth cones flattened down and extended filopodia-like processes. This behaviour was inhibited by cytochalasin B and reversibly by cold (4 degrees C). We conclude that physiologically active growth cones can be isolated rapidly and in large numbers by the method described here.

摘要

我们设计了一种从新生大鼠前脑分离有活力的神经元生长锥的方法。该方法包括差速离心和密度梯度离心,利用了生长锥相对较低的浮力密度(约1.018 g/cm³)。目前尚无已知的生长锥生化标志物,因此在分离过程中必须使用透射电子显微镜监测其存在。使用了几个标准来鉴定分离出的生长锥,包括丝状伪足的存在、广泛的分支系统、管状光滑内质网以及质膜下方富含微丝的区域。这些形态特征与在完整发育大脑和组织培养中明确鉴定出的生长锥相似。电子显微镜分析表明,根据这些标准,某一部分中超过90%的膜结合可识别物体是生长锥。主要污染物由来源不明的膜囊和小泡组成。只有少量分离的粗面内质网和线粒体。分离出的生长锥大致呈球形,直径为1.9±0.5微米(平均值±1标准差)。它们通常含有线粒体、大颗粒小泡和小泡,偶尔含有被膜小泡、溶酶体、板层小体和多囊泡体,很少含有中间丝。偶尔,生长锥上有原始突触。通过观察分离出的生长锥在短期培养中的行为来研究其活力。在聚-D-赖氨酸包被的盖玻片上培养数小时后,生长锥变平并伸出丝状伪足样突起。这种行为被细胞松弛素B抑制,被低温(4℃)可逆抑制。我们得出结论,通过本文所述方法可以快速大量分离出生理活性生长锥。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验