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Comparative analysis of apoptosis measured by Hoechst and flow cytometry in non-Hodgkin's lymphomas

机译:Hoechst法和流式细胞仪检测非霍奇金淋巴瘤细胞凋亡的比较分析

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Fine-needle samples of 75 non-Hodgkin's lymphomas R-ere investigated for apoptosis immediately and after 24 h of culture after in vitro irradiation (2 Gy, 10 Gy, and nonirradiated controls). Apoptotic cells were simultaneously quantified by fluorescence microscopic enumeration of apoptotic cells using Hoechst 33342 staining, and by flow cytometric detection of sub-G(1) peak cells, The nonirradiated controls showed a similar mean percent apoptotic cells using both methods, analyzed immediately (9% by morphology vs. 10% by flow) or after 24 h of culture (40% by morphology vs. 41% by flow). In the irradiated samples, the mean percent apoptotic cells quantified by morphology was higher than by flow cytometry (64% by morphology Fs. 55% by flow after 2 Gy irradiation, and 71% vs. 58% after 10 Gy), The results of the two methods were correlated, although large differences were seen between the techniques in individual tumors, In our system, flow cytometric sub-G(1) peak analysis appears to underestimate apoptosis, Of these two methods, we find the Hoechst morphology method to be more reliable for quantitation of apoptosis utilising fresh fine-needle sample material, in that discrimination of apoptotic cells from debris is easier and that both early and late apoptotic cells are detectable, (C) 1998 Wiley-Liss, Inc. [References: 35]
机译:立即对75例非霍奇金淋巴瘤R-ere的细针样本进行了研究,并在体外照射(2 Gy,10 Gy和未照射的对照)培养24小时后检查了细胞凋亡。通过使用Hoechst 33342染色的荧光显微镜下凋亡细胞的荧光显微镜枚举以及通过流式细胞术检测亚G(1)峰值细胞来同时对凋亡细胞进行定量。未照射的对照显示两种方法均显示出相似的平均凋亡百分数,立即进行分析(9形态学百分比为10%,流量为10%)或培养24小时后(形态学百分比为40%,流量为41%)。在经辐照的样品中,通过形态学定量的平均凋亡细胞百分率高于通过流式细胞仪(形态学Fs为64%,2 Gy辐照后为55%,10 Gy后为58%)。两种方法是相关的,尽管在单个肿瘤中使用的技术之间存在很大差异,但在我们的系统中,流式细胞仪sub-G(1)峰分析似乎低估了细胞凋亡。使用新鲜的细针头样品材料对凋亡的定量分析更可靠,因为更容易区分碎片中的凋亡细胞,并且可以检测早期和晚期凋亡细胞,(C)1998 Wiley-Liss,Inc. [References:35]

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