De Sucheta, Ehrlich Marcelo
Shmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.
Methods Mol Biol. 2025;2926:91-100. doi: 10.1007/978-1-0716-4542-0_8.
Immunofluorescence microscopy allows for the quantitative assessment of cell fate at single-cell resolution. This is required to analyze heterogeneous cell populations, as the assessment of average values of given parameters does not faithfully describe distinct states of specific subpopulations. As a case in point, we describe a methodology for characterizing the effects of a microtubule targeting agent, 2-methoxestradiol (2ME2), on T24 human bladder cancer cells. We employ an immunofluorescence-based assessment of nuclear morphology, DNA content, and the intracellular distribution pattern of microtubules for the identification/classification of cells undergoing mitosis or mitotic slippage. When combined with imaging-based identification of cells expressing a nonstructural oncolytic virus protein, this approach enables the assessment of the potential for combined treatment with a microtubule targeting agent and an oncolytic virus (e.g., the Epizootic Hemorrhagic Disease Virus-Tel Aviv University, EHDV-TAU).
免疫荧光显微镜能够在单细胞分辨率下对细胞命运进行定量评估。这对于分析异质性细胞群体是必要的,因为给定参数的平均值评估并不能如实描述特定亚群的不同状态。作为一个例子,我们描述了一种方法,用于表征微管靶向剂2-甲氧基雌二醇(2ME2)对T24人膀胱癌细胞的影响。我们采用基于免疫荧光的方法评估核形态、DNA含量以及微管的细胞内分布模式,以识别/分类经历有丝分裂或有丝分裂滑脱的细胞。当与基于成像的表达非结构溶瘤病毒蛋白的细胞识别相结合时,这种方法能够评估微管靶向剂与溶瘤病毒(例如,流行性出血病病毒-特拉维夫大学,EHDV-TAU)联合治疗的潜力。