McLean W G, Kanje M, Remgård P
Department of Pharmacology and Therapeutics, University of Liverpool, UK.
Brain Res. 1993 Jun 11;613(2):295-9. doi: 10.1016/0006-8993(93)90914-9.
Here we present a model system which for the first time permits studies of slow axonal transport in vitro. Axonally transported proteins of rat vagus nerves were radiolabelled with [35S]methionine in the nodose ganglion in vitro and were incubated for up to 3 days in culture medium. Slowly transported proteins were analyzed by one- and two-dimensional polyacrylamide gel electrophoresis and identified on Western blots of two-dimensional gels with antibodies to actin and alpha-tubulin. The system will be valuable for pharmacological analysis of the mechanisms of slow transport.
在此,我们展示了一个首次允许在体外研究轴突慢速运输的模型系统。大鼠迷走神经的轴突运输蛋白在体外结节神经节中用[35S]甲硫氨酸进行放射性标记,并在培养基中孵育长达3天。通过一维和二维聚丙烯酰胺凝胶电泳分析慢速运输的蛋白,并用抗肌动蛋白和α-微管蛋白抗体在二维凝胶的蛋白质印迹上进行鉴定。该系统对于慢速运输机制的药理学分析将具有重要价值。