Cornelissen F, Nuyens R, Nuydens R, Geerts H
Department of Life Sciences, Janssen Research Foundation, Beerse, Belgium.
J Neurosci Methods. 1990 Oct;35(1):79-88. doi: 10.1016/0165-0270(90)90097-y.
A method is presented which allows the automatic quantification of the fast axonal transport of endogenous organelles in neurites of cultured neuronal cells. Stretches of videotape recordings from Allen video enhanced contrast (AVEC) microscopy are digitized by currently available image processor hardware and analysed off-line on a MicroVAX II. Movements along the axon are calculated in great detail, allowing statistically significant changes to be detected. Interaction from the operator is minimised, thereby bypassing tedious manual analysis. This paper further reports the application of this system to the effect of vanadate treatment on axonal transport in cultures of rat embryonic hippocampal neurons.
本文介绍了一种能够自动定量培养神经元细胞神经突中内源性细胞器快速轴突运输的方法。来自艾伦视频增强对比度(AVEC)显微镜的录像片段由现有的图像处理器硬件进行数字化处理,并在MicroVAX II上进行离线分析。沿轴突的运动被详细计算,从而能够检测到具有统计学意义的变化。操作人员的干预被降至最低,从而避免了繁琐的手动分析。本文还进一步报道了该系统在钒酸盐处理对大鼠胚胎海马神经元培养物中轴突运输影响方面的应用。