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High‐potentiality preliminary selection criteria and transformation time‐dependent factors analysis for establishing Epstein–Barr virus transformed human lymphoblastoid cell lines

机译:建立Epstein-Barr病毒转化人淋巴母细胞细胞系的高潜力初步选择标准和转化时间相关因素分析

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摘要

Infection of freshly isolated and cryopreserved lymphocytes with Epstein–Barr virus (EBV) leads to the establishment of human B lymphoblastoid cell lines (LCLs). Techniques for optimal infection of the lymphocytes are vital for the establishment of a human biobank. The present study found that more than half (58–86%) of such established LCLs had transport times of less than 48 h, cell densities exceeding 10 cells/ml and cell viabilities greater than 90%. After EBV infection, 3306 freshly isolated lymphocytes required 30.0 ± 0.1 days to become LCLs. Conversely, 1210 cryopreserved lymphocytes required 36.2 ± 0.4 days. Cell density and viability of the culture affected transformation time in freshly isolated lymphocytes. On the other hand, blood transport time, cryopreservation time and initial cell viability were major factors in cryopreserved specimens. These results contribute to general information concerning the establishment of a human biobank for EBV infected cells.
机译:用爱泼斯坦-巴尔病毒(EBV)感染新鲜分离和冷冻的淋巴细胞会导致人类B淋巴母细胞样细胞系(LCL)的建立。淋巴细胞最佳感染的技术对于建立人类生物库至关重要。本研究发现,此类已建立的LCL中有一半以上(58-86%)的运输时间少于48小时,细胞密度超过10个细胞/ ml,细胞活力大于90%。 EBV感染后,需要30.0±0.1天的时间才能将3306个新鲜分离的淋巴细胞变成LCL。相反,1210个冷冻保存的淋巴细胞需要36.2±0.4天。培养物的细胞密度和活力影响新鲜分离的淋巴细胞中的转化时间。另一方面,血液运输时间,冷冻保存时间和初始细胞活力是冷冻保存标本中的主要因素。这些结果有助于获得有关为EBV感染的细胞建立人类生物库的一般信息。

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