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[47例染色体核型异常患者永久性淋巴母细胞系的建立]

[Establishment of permanent lymphoblastoid cell lines of 47 patients with abnormal chromosome karyotype].

作者信息

Liao Shi-Xiu, Wang Ying-Tai, Yang Yan-Li, Li Yi, Huang Fei-Fei, Hao Bing-Tao, Wang Zhao-Cai, Zhu Wen-Yu, Si Yan-Mei, Wang Ya-Juan

机构信息

Institute of Medical Genetics, Henan Province People's Hospital, Zhengzhou 450003, China.

出版信息

Yi Chuan Xue Bao. 2002 Apr;29(4):303-6.

Abstract

To increase the efficiency of in vitro transformation of human lymphocytes by Epstein-Barr virus (EBV) and establish permanent lymphoblastoid cell lines from patients with abnormal chromosome karyotype, B lymphoid cells were prepared from cryopreserved heparinized blood samples. The lymphoid cell pellet was resuspended with 0.5 ml medium of RPMI with 20% fetal calf serum(FCS), and added 2 ml virus-containing superatant of the EB virus-producing cell lines by filtrated, and mixed. Four 25 cm2 cell culture bottles were put upright. A total of 2.5 ml of RPMI with 20% FCS was put in each of them. The blood-virus mixture was distributed among the four cell culture bottles as follows: Bottle I, Bottle II, Bottle III and Bottle IV were added with 0.3 ml, 0.6 ml, 1.2 ml and the rest respectively. The cells culture bottles were put into the cell culture incubator in an upright position. After 3 days the cells were puting new medium with 20% FCS as follows: Bottle I 3 ml, Bottle II 4 ml, Bottle III 5 ml and Bottle IV 6 ml. After one week, the medium was changed again as described above. The medium change was conducted until the cells grew very fast. The right ratio between blood cells and virus titer can not be exactly determined for every blood sample, and therefore a dilution series with four different blood/virus ratios was set up. Due to the dilution series, addition of immune inhibitors like cyclosporine, was not necessary. Forty-seven permanent lymphoblastoid cell lines of patients with abnormal chromosome karyotype. Transformed cells were found in only one or two of the four cell culture bottles. The total successive rate increased up to 97.87%. Of the four cell culture bottles, Bottle I, Bottle II, Bottle III and Bottle IV, the successive rates were 6.39%, 61.70%, 31.91% and 8.51% respectively. This method can be used for preserving large number of lymphoblastoid cell lines, and also provide enough research materials for further studies.

摘要

为提高爱泼斯坦 - 巴尔病毒(EBV)体外转化人淋巴细胞的效率,并从染色体核型异常的患者中建立永久性淋巴母细胞系,从冷冻保存的肝素化血样中制备B淋巴细胞。将淋巴样细胞沉淀重悬于0.5 ml含20%胎牛血清(FCS)的RPMI培养基中,加入2 ml经滤过的EB病毒生产细胞系的含病毒上清液,并混合。将四个25 cm²细胞培养瓶直立放置。每个培养瓶中加入2.5 ml含20% FCS的RPMI。将血 - 病毒混合物按如下方式分配到四个细胞培养瓶中:I瓶、II瓶、III瓶和IV瓶分别加入0.3 ml、0.6 ml、1.2 ml和其余部分。将细胞培养瓶直立放入细胞培养箱中。3天后,给细胞更换含20% FCS的新培养基,如下:I瓶3 ml,II瓶4 ml,III瓶5 ml,IV瓶6 ml。一周后,按上述方法再次更换培养基。持续更换培养基直至细胞生长非常迅速。由于每个血样无法准确确定血细胞与病毒滴度之间的正确比例,因此设置了四个不同血/病毒比例的稀释系列。由于采用了稀释系列,无需添加环孢素等免疫抑制剂。染色体核型异常患者的47个永久性淋巴母细胞系。仅在四个细胞培养瓶中的一两个中发现了转化细胞。总成功率提高到97.87%。在四个细胞培养瓶I瓶、II瓶、III瓶和IV瓶中,成功率分别为6.39%、61.70%、31.91%和8.51%。该方法可用于保存大量淋巴母细胞系,也为进一步研究提供了足够的研究材料。

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