Institute of Apply Genomics, Fuzhou University, Fuzhou, China.
School of Basic Medical Sciences, Fujian Medical University, Fuzhou, China.
J Cell Mol Med. 2019 Jan;23(1):227-236. doi: 10.1111/jcmm.13923. Epub 2018 Oct 24.
HeLa cells are a commonly used cell line in many biological research areas. They are not picky for culture medium and proliferate rapidly. HeLa cells are a notorious source of cell cross-contamination and have been found to be able to contaminate a wide range of cell lines in cell culture. In this study, we reported a simple and efficient method for detecting the presence of HeLa cell contamination in cell culture. HPV-18 was used as a biomarker. The cell culture supernatant was used directly as the template for nested PCR without extracting nucleic acid. By PCR amplification of the cell culture supernatant with the designed primers, we were able to detect the presence of HeLa cells in the culture. The sensitivity of this method can reach 1%, which is 10-fold higher than Short tandem repeat sequence (STR) profiling. This simple, rapid, and "noninvasive" quality checking method should find applications in routine cell culture practice.
HeLa 细胞是许多生物学研究领域中常用的细胞系。它们对培养基没有特别的要求,并且繁殖迅速。HeLa 细胞是细胞交叉污染的臭名昭著的来源,并且已经发现能够污染细胞培养中的广泛的细胞系。在这项研究中,我们报告了一种简单而有效的方法,用于检测细胞培养中 HeLa 细胞污染的存在。HPV-18 被用作生物标志物。细胞培养上清液直接用作巢式 PCR 的模板,而无需提取核酸。通过用设计的引物对细胞培养上清液进行 PCR 扩增,我们能够检测到培养物中 HeLa 细胞的存在。该方法的灵敏度可达 1%,比短串联重复序列(STR)分析高 10 倍。这种简单、快速且“非侵入性”的质量检查方法应该在常规细胞培养实践中得到应用。