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Observation and quantification of the morphological effect of trypan blue rupturing dead or dying cells

机译:检测和定量逆杂交死亡或死亡细胞的形态学效应

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Trypan blue has long been the gold standard for staining dead cell to determine cell viability. The dye is excluded from membrane-intact live cells, but can enter and concentrate in membrane-compromised dead cells, rendering the cells dark blue. Over the years, there has been an understanding that trypan blue is inaccurate for cell viability under 80% without scientific support. We previously showed that trypan blue can alter the morphology of dead cells to a diffuse shape, which can lead to over-estimation of viability. Here, we investigate the origin of the dim and diffuse objects after trypan blue staining. Utilizing image and video acquisition, we show real-time transformation of cells into diffuse objects when stained with trypan blue. The same phenomenon was not observed when staining cells with propidium iodide. We also demonstrate the co-localization of trypan blue and propidium iodide, confirming these diffuse objects as cells that contain nuclei. The videos clearly show immediate cell rupturing after trypan blue contact. The formation of these diffuse objects was monitored and counted over time as cells die outside of the incubator. We hypothesize and demonstrate that rapid water influx may have caused the cells to rupture and disappear. Since some dead cells disappear after trypan blue staining, the total can be under-counted, leading to over-estimation of cell viability. This inaccuracy could affect the outcomes of cellular therapies, which require accurate measurements of immune cells that will be infused back into patients.
机译:台盼蓝长期以来一直是染色死池的金标准,以确定细胞活力。染料被排除在膜完整的活细胞之外,但可以在膜受损的死细胞中进入和浓缩,使细胞深蓝色。多年来,有一种理解,在没有科学的支持下,在80%以下的细胞存活率下,锥虫蓝是不准确的。我们以前表明,台盼蓝可以改变死细胞的形态,以弥漫形状,这可能导致过度估计可行性。在这里,我们研究了台盼蓝染色后昏暗和漫反射物体的起源。利用图像和视频采集,我们将细胞的实时转换与台盼蓝染色时的漫射物体。当碘化丙锭染色细胞时未观察到相同的现象。我们还证明了台盼蓝和碘化丙锭的共定位,确认这些漫反射物作为含有核的细胞。视频清楚地显示了台盼蓝接触后立即细胞破裂。随着细胞死在培养箱外面的情况下,监测这些漫射物体的形成并计数。我们假设并证明快速的水流入可能导致细胞破裂并消失。由于一些死细胞在台盼蓝染色后消失,因此可以估计总量,从而导致细胞活力过度估计。这种不准确可能会影响细胞疗法的结果,这需要准确测量将被注入患者的免疫细胞。

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