Bilsland J, Rigby M, Young L, Harper S
Department of Pharmacology, Merck, Sharp and Dohme Laboratories, Neuroscience Research Centre, Harlow, Essex, UK.
J Neurosci Methods. 1999 Oct 15;92(1-2):75-85. doi: 10.1016/s0165-0270(99)00099-0.
Neurite outgrowth from dorsal root ganglion (DRG) explants is a method of evaluating neurotrophic activity of growth factors and neurotrophin mimetics. The drawbacks to this approach are the difficulties in quantifying the response. Neurite counts are time consuming and labour intensive, and the accuracy is often questionable due to branching and fasciculation of the neurites. We report here a method of semi-quantitative analysis of neurite outgrowth from chick DRG explants, using image analysis to quantify the area occupied by neurites emanating from the ganglion. This method is rapid, takes into account both the length and number of neurites, and is unaffected by neurite fasciculation or branching. Primary explants of chick DRGs were treated with the neurotrophins nerve growth factor (NGF) or neurotrophin-3 (NT-3) and with the compound K252a. K252b was tested for potentiation of the response to NT-3. The results show a dose dependent outgrowth of neurites from explants treated with NGF, NT-3 and K252a, and potentiation of the NT-3 response by K252b. These responses were quantified by neurite area quantification using image analysis. We conclude that neurite area measurement using image analysis provides a robust means of evaluating neurotrophic activity of growth factors and neurotrophin mimetics in vitro.
背根神经节(DRG)外植体的神经突生长是一种评估生长因子和神经营养素模拟物神经营养活性的方法。这种方法的缺点是难以量化反应。神经突计数既耗时又费力,而且由于神经突的分支和束状化,其准确性往往值得怀疑。我们在此报告一种对鸡DRG外植体神经突生长进行半定量分析的方法,使用图像分析来量化从神经节发出的神经突所占的面积。该方法快速,兼顾了神经突的长度和数量,且不受神经突束状化或分支的影响。鸡DRG的原代外植体用神经营养因子神经生长因子(NGF)或神经营养素-3(NT-3)以及化合物K252a进行处理。测试了K252b对NT-3反应的增强作用。结果显示,用NGF、NT-3和K252a处理的外植体神经突呈剂量依赖性生长,并且K252b增强了NT-3反应。这些反应通过使用图像分析的神经突面积量化来进行定量。我们得出结论,使用图像分析测量神经突面积为体外评估生长因子和神经营养素模拟物的神经营养活性提供了一种可靠的方法。