Ayyoob Khosravi, Masoud Khoshnia, Vahideh Kazeminejad, Jahanbakhsh Asadi
Department of Molecular Medicine, Faculty of Advanced Medical Technologies, Golestan University of Medical Sciences, Gorgan, Iran.
Golestan Research Center of Gastroenterology and Hepatology-GRCGH, Golestan University of Medical Sciences, Gorgan, Iran.
Tumour Biol. 2016 Mar;37(3):3197-204. doi: 10.1007/s13277-015-4133-4. Epub 2015 Oct 2.
Cross-contamination during or early after establishment of a new cell line could result in the worldwide spread of a misidentified cell line. Therefore, newly established cell lines need to be authenticated by a reference standard method. This study was conducted to investigate the authenticity of a newly established epithelial cell line of human esophageal squamous cell carcinoma (ESCC) called YM-1 using short tandem repeat (STR) DNA profiling method. Primary human ESCC epithelial cells were cultured from the fresh tumor tissue of an adult female patient. Growth characteristics and epithelial originality of YM-1 cells were studied. Genomic DNA was isolated from YM-1 cells harvested at passage 22 and ESCC donor tumor sample on two different days to prevent probable DNA contamination. STR profiling was performed using AmpFℓSTR® Identifiler® Plus PCR Amplification Kit. To address whether YM-1 cells undergo genetic alteration as the passage number increases, STR profiling was performed again on harvested cells at passage 51. YM-1 cells grew as a monolayer with a population doubling time of 40.66 h. Epithelial originality of YM-1 cells was confirmed using ICC/IF staining of cytokeratins AE1/AE3. The STR profile of the ESCC donor tumor sample was the same with YM-1 cells at passage 22. However, STR profile of the donor tumor sample showed an off-ladder (OL) allele in their D7S820 locus. Also, re-profiling of YM-1 cells at passage 51 showed a loss of heterozygosity (LOH) at D18S51 locus. This suggests that long-term culture of cell lines may alter their DNA profile. Comparison of the DNA fingerprinting results in DSMZ, and ATCC STR profiling databases confirmed unique identity of YM-1 cell line. This study provides an easy, fast, and reliable procedure for authentication of newly established cell lines, which helps in preventing the spread of misidentified cells and improving the reproducibility and validity of experiments, consequently.
新细胞系建立期间或建立后早期的交叉污染可能导致错误识别的细胞系在全球范围内传播。因此,新建立的细胞系需要通过参考标准方法进行鉴定。本研究旨在使用短串联重复序列(STR)DNA 分析方法调查一种新建立的人食管鳞状细胞癌(ESCC)上皮细胞系 YM-1 的真实性。从一名成年女性患者的新鲜肿瘤组织中培养原代人 ESCC 上皮细胞。研究了 YM-1 细胞的生长特性和上皮来源。在两天不同时间从第 22 代收获的 YM-1 细胞和 ESCC 供体肿瘤样本中分离基因组 DNA,以防止可能的 DNA 污染。使用 AmpFℓSTR® Identifiler® Plus PCR 扩增试剂盒进行 STR 分析。为了研究 YM-1 细胞是否随着传代次数增加而发生基因改变,对第 51 代收获的细胞再次进行 STR 分析。YM-1 细胞呈单层生长,群体倍增时间为 40.66 小时。使用细胞角蛋白 AE1/AE3 的免疫细胞化学/免疫荧光染色确认了 YM-1 细胞的上皮来源。ESCC 供体肿瘤样本的 STR 图谱与第 22 代的 YM-1 细胞相同。然而,供体肿瘤样本的 STR 图谱在其 D7S820 位点显示出一个非标准(OL)等位基因。此外,第 51 代 YM-1 细胞的重新分析显示在 D18S51 位点出现杂合性缺失(LOH)。这表明细胞系的长期培养可能会改变其 DNA 图谱。将 DNA 指纹图谱结果与 DSMZ 和 ATCC STR 分析数据库进行比较,证实了 YM-1 细胞系的独特身份。本研究为新建立的细胞系鉴定提供了一种简单、快速且可靠的方法,有助于防止错误识别细胞的传播,从而提高实验的可重复性和有效性。