Tierrablanca-Sánchez Lilia, Pérez Medina Martínez Víctor, Ramírez Ibañez Nancy D, Pérez Ramírez Néstor O, Flores Ortiz Francisco Luis, Medina-Rivero Emilio
Research and Development, Probiomed.
Research and Development, Probiomed;
J Vis Exp. 2017 Sep 16(127):55376. doi: 10.3791/55376.
This protocol shows the measurement of the apoptotic activity neutralization of TNFα in a mouse fibroblast cell model (WEHI 164) using an anti-TNFα mAb. In addition, this protocol can be used to evaluate other anti-TNFα molecules, such as fusion proteins. The cellular model employed here is sensitive to TNFα-mediated apoptosis when an additional stress factor is induced in cell culture conditions (e.g., serum deprivation). This procedure exemplifies how to execute this analytical assay, highlighting the key operations relating to the sample preparation, cell dilution, apoptosis induction, and spectrophotometric measurements that are critical to ensure successful results. This protocol reveals the best-performance conditions relating to apoptosis induction and efficient signal recording, leading to low uncertainty values.
本方案展示了在小鼠成纤维细胞模型(WEHI 164)中使用抗TNFα单克隆抗体测量TNFα凋亡活性中和作用的方法。此外,该方案可用于评估其他抗TNFα分子,如融合蛋白。当在细胞培养条件下诱导额外的应激因素(如血清剥夺)时,此处使用的细胞模型对TNFα介导的凋亡敏感。本程序举例说明了如何进行这种分析测定,重点介绍了与样品制备、细胞稀释、凋亡诱导和分光光度测量相关的关键操作,这些操作对于确保获得成功结果至关重要。本方案揭示了与凋亡诱导和有效信号记录相关的最佳性能条件,从而产生低不确定性值。