Jap Tjoen San E R, Schmidt-Michels M H, Spruijt B M, Oestreicher A B, Schotman P, Gispen W H
Division of Molecular Neurobiology, Rudolf Magnus Institute, University of Utrecht, The Netherlands.
J Neurosci Res. 1991 Jun;29(2):149-54. doi: 10.1002/jnr.490290203.
A combined assay to measure neurite outgrowth and B-50/GAP-43 levels in PC12 cells is reported. During NGF-induced neuritogenesis, B-50/GAP-43 expression was monitored by enzyme-linked immunosorbent assay (ELISA). Neurite outgrowth was quantified at the same time by the use of video image analysis. Sensitivity and reliability of the methods are shown with a dose-response and time curve of beta-NGF-induced neuritogenesis. A linear increase in total length of neurites was induced by concentrations of beta-NGF greater than or equal to 5 ng/ml and was accompanied by a linear increase in the amount of B-50/GAP-43. The combined methods presented here can conveniently and reliably establish subtle changes in neurite outgrowth and intracellular protein contents.
报道了一种用于测量PC12细胞中神经突生长和B-50/GAP-43水平的联合检测方法。在神经生长因子(NGF)诱导的神经突形成过程中,通过酶联免疫吸附测定(ELISA)监测B-50/GAP-43的表达。同时利用视频图像分析对神经突生长进行定量。通过β-NGF诱导神经突形成的剂量反应和时间曲线展示了这些方法的灵敏度和可靠性。浓度大于或等于5 ng/ml的β-NGF可诱导神经突总长度呈线性增加,并伴随着B-50/GAP-43量的线性增加。这里介绍的联合方法能够方便且可靠地确定神经突生长和细胞内蛋白质含量的细微变化。