首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Two epithelial tumor cell lines (HNE-1 and HONE-1) latently infected with Epstein-Barr virus that were derived from nasopharyngeal carcinomas.
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Two epithelial tumor cell lines (HNE-1 and HONE-1) latently infected with Epstein-Barr virus that were derived from nasopharyngeal carcinomas.

机译:来自鼻咽癌的两种上皮性肿瘤细胞系(HNE-1和HONE-1)被Epstein-Barr病毒潜伏感染。

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摘要

Two epithelial tumor cell lines were established from biopsy specimens of nasopharyngeal carcinomas (NPC). The specimens were taken from poorly differentiated squamous cell carcinomas of the nasopharynx. The tissues were prepared for cell culture and eventually two continuous epithelial cell lines were obtained and designated HONE-1 and HNE-1. Light and electron microscopic examination of these two cell lines demonstrated cells with an epithelial morphology including the presence of desmosomes. The HNE-1 cell line has been passaged more than 100 times and the HONE-1 cell line has been passaged more than 90 times. It was found that early-passage uncloned HNE-1 cells (passage 23) could be superinfected with the B95-8 and NPC-EBV isolates as demonstrated by the induction of Epstein-Barr virus (EBV)-specific early antigen(s) in a small percentage of the cells; HONE-1 cells could also be superinfected with EBV. Southern blot analysis detected EBV DNA in samples from uncloned HNE-1 cells at passages 12, 17, 21, 27, and 35. However, by passage 45, EBV DNA could no longer be detected in HNE-1 cells by Southern blot analysis. The EBV genome was detected in parental HONE-1 cells at subculture 9 and in clone 40 cells up to passage 40 thus far. When HNE-1 cells were examined for the expression of the EBV-encoded nuclear antigen (EBNA) at passage 12, only about 10% of the cells were found to be positive. The percentage of EBNA-positive HNE-1 cells decreased as the cells were passaged. A similar loss of EBNA was observed in uncloned HONE-1 cells, but not in HONE-1 clone 40 cells. In clone 40, which has been passaged 40 times thus far, 85-90% of the cells are still EBNA-positive. The data suggest that EBV genome-positive HNE-1 and HONE-1 cells were lost as the cells were cultivated in vitro and that cloning the cells at an early passage level may be critical in maintaining EBV genome-positive epithelial NPC cells. These EBV genome-positive epithelial NPC cell lines will be useful for studying the association of EBV and NPC.
机译:从鼻咽癌(NPC)的活检标本中建立了两种上皮肿瘤细胞系。标本取自鼻咽低分化鳞状细胞癌。准备组织用于细胞培养,并最终获得两个连续的上皮细胞系,并命名为HONE-1和HNE-1。对这两种细胞系的光镜和电镜检查表明细胞具有上皮形态,包括桥粒的存在。 HNE-1细胞系已传代100多次,而HONE-1细胞系已传代90多次。已发现,早期传代的未克隆HNE-1细胞(第23代)可能会被B95-8和NPC-EBV分离株超感染,如通过在爱因斯坦-巴尔病毒(EBV)特异性早期抗原中的诱导所证明的那样。一小部分细胞; HONE-1细胞也可以被EBV感染。 Southern印迹分析在第12、17、21、27和35代中检测到未克隆的HNE-1细胞样本中的EBV DNA。但是,通过45代,Southern印迹分析不再能在HNE-1细胞中检测到EBV DNA。迄今为止,在传代培养9的亲本HONE-1细胞和直到40代的克隆40细胞中均检测到EBV基因组。在第12代检查HNE-1细胞的EBV编码核抗原(EBNA)的表达时,仅发现约10%的细胞为阳性。 EBNA阳性HNE-1细胞的百分比随细胞传代而降低。在未克隆的HONE-1细胞中观察到类似的EBNA丧失,但在HONE-1克隆40细胞中未观察到。迄今已传代40次的克隆40中,仍有85-90%的细胞为EBNA阳性。数据表明,在体外培养时,EBV基因组阳性的HNE-1和HONE-1细胞丢失,并且在早期传代水平克隆细胞对于维持EBV基因组阳性的上皮NPC细胞可能至关重要。这些EBV基因组阳性的上皮NPC细胞系将有助于研究EBV与NPC的关联。

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