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EB病毒潜伏感染的套细胞淋巴瘤模型研究
引用本文:金在顺,安锦丹,宋华林,吕强,曹永,于建渤,郭素芬,郑慧哲. EB病毒潜伏感染的套细胞淋巴瘤模型研究[J]. 中国肿瘤临床, 2012, 39(1): 1-4. DOI: 10.3969/j.issn.1000-8179.2012.01.001
作者姓名:金在顺  安锦丹  宋华林  吕强  曹永  于建渤  郭素芬  郑慧哲
作者单位:①.牡丹江医学院,黑龙江省高校肿瘤疾病防治重点实验室(黑龙江省牡丹江市157011)
基金项目:黑龙江省教育厅海外学人重点科研项目(编号:1152hz36)资助~~
摘    要:   目的   建立EBV潜伏感染的套细胞淋巴瘤模型,为淋巴瘤预防与治疗的研究奠定基础。   方法  利用新霉素耐性的重组遗传基因EBV(NeoR EBV)和B95-8 EBV对套细胞淋巴瘤细胞株SP49、SP53和Jeko-1进行感染,选出EBV阳性的MCL细胞株,采用免疫荧光法和Southern blot进行鉴定,采用Western blot和流式细胞仪检测EBV阳性的MCL细胞株的免疫表型及生物学活性。   结果  成功获得SP49/EBV、SP53/EBV细胞株,均表达EBER1、EBNA2和LMP1,其免疫表型只有CD38表达增强,两细胞株均具有低增殖功能,凋亡抵抗性,成瘤能力下降等特点。   结论  本研究建立的SP49/EBV和SP53/EBV细胞株,具有体内EBV潜伏感染的静息B细胞低增殖活性的特征,可成为研究体内EBV潜伏感染的良好模型。 

关 键 词:EB病毒   潜伏感染   静息B细胞   套细胞淋巴瘤
收稿时间:2011-09-27

EB Virus Latent Infection of Mantle Cell Lymphoma Model
Zaishun JIN,Jindan AN,Hualin SONG,Qiang LV,Yong CAO,Jianbo YU,Sufen GUO,Huizhe ZHENG. EB Virus Latent Infection of Mantle Cell Lymphoma Model[J]. Chinese Journal of Clinical Oncology, 2012, 39(1): 1-4. DOI: 10.3969/j.issn.1000-8179.2012.01.001
Authors:Zaishun JIN  Jindan AN  Hualin SONG  Qiang LV  Yong CAO  Jianbo YU  Sufen GUO  Huizhe ZHENG
Affiliation:①.Key Laboratory of Cancer Prevention and Treatment of Heilongjiang Province, Mudanjiang Medical University, Mudanjiang 157011, China②.Department of Pathology, Basic Medical College, Mudanjiang Medical University, Mudanjiang 157011, China
Abstract:   Objective  To establish a mantle cell lymphoma (MCL) model latently infected by EBV for researches of prevention and treatment of lymphoma.   Methods  Neomycin resistant recombinant EBV (NeoR EBV) and B95-8 EBV genes were used to infect B cell lines of SP49, SP53 and Jeko-1. EBV-positive MCL cell lines were selected through immunofluorescence and Southern blot. The immune phenotypes and biological activities of EBV-positive MCL cell lines were detected by Western blot and flow cytometry.   Results  SP49/EBV and SP53/EBV cell lines expressing EBER1, EBNA2 and LMP1 were successfully established, with only enhanced CD38 immune phenotype. The abilities of proliferation, apoptotic resistance as well as tumor forming decreased in both cell lines.   Conclusion  SP49/EBV and SP53/EBV cell lines established in this study were characterized with lower abilities of proliferation similar to resting B cells latently infected by EBV in vivo. Therefore the above cell lines may be good models of research for latent EBV infection in vivo. 
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