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B-cell lymphoma line (Raji) viability and surface marker expression minimally affected by 20- and 25-gauge vitrectomy systems analyzed by flow cytometry.

机译:B细胞淋巴瘤细胞系(Raji)的生存能力和表面标志物表达受流式细胞仪分析的20和25规格玻璃体切除系统的影响最小。

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PURPOSE: The purpose of this study was to evaluate the effect of 20-gauge (20-G) and 25-gauge (25-G) vitrectomy on cell viability and diagnostic yield (surface marker expression) using flow cytometry and human lymphoma cells in culture. METHODS: Cultured human Burkitt lymphoma cells (Raji B-cell lymphoma line) were allocated into five study groups in Roswell Park Memorial Institute media. By using manual aspiration, cells were then processed by aspiration alone, by 20-G vitrectomy at 600 cuts per minute (cpm) and 1,500 cpm, or by 25-G vitrectomy at both 600 and 1,500 cpm. To assess cell viability and cell surface marker expression, samples underwent standard flow cytometry analysis for suspected lymphoma using 7-amino-actinomycin D and antibodies against CD45, CD19, lambda, and kappa light chains. RESULTS: Twenty-five samples were processed after being divided into four vitrectomy groups and one nonvitrectomy group (control). The mean cell viability was 98.5 for both the nonvitrectomized and vitrectomized specimens. The percentage of cells positive for CD45 or kappa light chain was the same in the nonvitrectomized and vitrectomized groups. In addition, the level of expression of these molecules was not significantly different in all five groups. Similarly, no difference was seen for these markers between 20-G and 25-G vitrectomy at either a cut rate of 600 or 1,500 cpm. The percentage positive for CD19 was significantly lower for the 20-G vitrectomy at 1,500 cpm compared with the 25-G vitrectomy at both 600 and 1,500 cpm. Percentage of CD19 cells was greater for the 25-G vitrectomy at 600 cpm than the nonvitrectomy group. CONCLUSION: Compared with simple aspiration, both 20-G and 25-G vitrectomy seem to have no significant effect on cell viability or diagnostic yield for B-cell lymphoma cells (Raji cell line) in suspension based on flow cytometry. Further studies need to be conducted to study and compare 20-G versus 25-G vitrectomy on lymphoma cells in human vitreous or in an animal model.
机译:目的:本研究的目的是使用流式细胞仪和人类淋巴瘤细胞评估20规格(20-G)和25规格(25-G)玻璃体切除术对细胞活力和诊断产量(表面标志物表达)的影响。文化。方法:将培养的人类伯基特淋巴瘤细胞(Raji B细胞淋巴瘤细胞系)分配到罗斯威尔公园纪念学院培养基中的五个研究组中。通过使用手动抽吸,然后仅通过抽吸,在600割/分钟(cpm)和1,500 cpm下进行20-G玻璃体切割术或在600和1,500 cpm下进行25-G玻璃体切割术来处理细胞。为了评估细胞活力和细胞表面标志物的表达,使用7-氨基放线菌素D和针对CD45,CD19,λ和kappa轻链的抗体,对可疑淋巴瘤进行标准流式细胞术分析。结果:将25份样品分为四个玻璃体切除术组和一个非玻璃体切除术组(对照组),进行了处理。未玻璃化和玻璃化的标本的平均细胞活力均为98.5。在未玻璃化和玻璃化切除的组中,CD45或κ轻链阳性的细胞百分比相同。另外,在所有五个组中这些分子的表达水平没有显着差异。同样,在切割速度为600或1,500 cpm的情况下,在20-G和25-G玻璃体切割术中,这些标记物也没有差异。 20-G玻璃体切割术在1,500 cpm时CD19阳性百分比显着低于25-G玻璃体切割术在600和1,500 cpm时。 25 c玻璃体切割术在600 cpm时CD19细胞百分比高于非玻璃体切除术组。结论:与单纯抽吸相比,基于流式细胞术的20-G和25-G玻璃体切除术似乎对悬浮的B细胞淋巴瘤细胞(Raji细胞系)的细胞存活率或诊断产率无明显影响。有必要进行进一步的研究,以研究和比较玻璃体或动物模型中的淋巴瘤细胞的20-G与25-G玻璃体切除术。

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