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爱泼斯坦-巴尔病毒潜伏基因表达对皮质酮和2-氯脱氧腺苷(2-CDA)在B细胞系中诱导凋亡作用的影响。

Influence of Epstein-Barr virus latent gene expression on the apoptosis-inducing effects of cortisone and 2-chlorodeoxyadenosine (2-CDA) in B-cell lines.

作者信息

Röth A, Pfaff P, Lange W, Finke J

机构信息

Department of Hematology and Oncology, University of Freiburg Medical Center, Germany.

出版信息

Cytokines Mol Ther. 1996 Mar;2(1):21-8.

PMID:9384686
Abstract

Burkitt's lymphoma (BL) cell lines are heterogenous with regard to phenotype, growth characteristics, Epstein-Barr virus (EBV) latent gene and BCL-2 expression. Previously we have demonstrated that transfection with the EBV genes LMP or EBNA-2 upregulates BCL-2 in B-cell lines. In order to test the functional relevance of these findings, cell lines were examined with regard to their sensitivity towards different apoptosis-inducing agents. BL cell lines transfected with LMP expressed high levels of BCL-2, and were compared with the parental cell line expressing little or no BCL-2. We also studied EBV immortalized lymphoblastoid cell lines (LCL) with high BCL-2 expression and strong resistance towards low serum concentrations. Hydrocortisone (HC) and 2-chlorodeoxyadenosine (2-CDA) were used alone or in different combinations. Cell growth and apoptosis were studied morphologically and by determination of viability and DNA fragmentation. BL cell lines showed different sensitivity towards HC-induced apoptosis, and sensitive cell lines became more resistant towards HC after infection with EBV or transfection with LMP and subsequent upregulation of BCL-2 expression. BL cell lines and LCL were relatively insensitive towards 2-CDA-induced apoptosis, and high concentrations of 2-CDA were necessary, independently of the levels of BCL-2 expression. In contrast to low-grade non-Hodgkin's lymphomas, 2-CDA does not appear to be a valuable drug for the treatment of Burkitt's lymphoma. LMP expression provides resistance towards hydrocortisone-induced apoptosis in vitro, possible through upregulation of BCL-2.

摘要

伯基特淋巴瘤(BL)细胞系在表型、生长特性、爱泼斯坦-巴尔病毒(EBV)潜伏基因及BCL-2表达方面存在异质性。此前我们已证明,用EBV基因LMP或EBNA-2转染可上调B细胞系中的BCL-2。为了检验这些发现的功能相关性,我们检测了细胞系对不同凋亡诱导剂的敏感性。转染LMP的BL细胞系表达高水平的BCL-2,并与几乎不表达或不表达BCL-2的亲代细胞系进行比较。我们还研究了具有高BCL-2表达且对低血清浓度有强抗性的EBV永生化淋巴母细胞系(LCL)。单独或联合使用氢化可的松(HC)和2-氯脱氧腺苷(2-CDA)。通过形态学观察以及活力测定和DNA片段化分析来研究细胞生长和凋亡情况。BL细胞系对HC诱导的凋亡表现出不同的敏感性,敏感细胞系在感染EBV或转染LMP并随后上调BCL-2表达后对HC的抗性增强。BL细胞系和LCL对2-CDA诱导的凋亡相对不敏感,且无论BCL-2表达水平如何,都需要高浓度的2-CDA。与低度非霍奇金淋巴瘤不同,2-CDA似乎不是治疗伯基特淋巴瘤的有效药物。LMP表达可能通过上调BCL-2在体外赋予对氢化可的松诱导凋亡的抗性。

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