RIKEN Cell Bank, Cell Engineering Division, BioResource Research Center, Tsukuba, Japan.
JCRB Cell Bank, National Institutes of Biomedical Innovation, Health and Nutrition, Osaka, Japan.
Int J Cancer. 2022 Aug 1;151(3):463-472. doi: 10.1002/ijc.34019. Epub 2022 Apr 19.
THP-1 is a representative leukemia cell line and is registered with four different numbers in JCRB and RIKEN BRC cell banks. However, differences between these four lines remain unclear. In our study, these four THP-1 cell lines, JCRB0112, JCRB0112.1 (corresponding to ATCC TIB-202), RCB1189 (DSMZ ACC-16) and RCB3686, have been compared at chromosome and DNA sequence levels. Our results reveal that ploidy has been changed in JCRB0112 and RCB1189, which are triploid and tetraploid, respectively. Patterns of variant frequencies from target sequencing are unique to each ploidy, estimating whole genomic status based on partial sequence data. SNP microarrays showed four distinct profiles with a large-scale loss of heterozygosity, reflected in subtle differences in STR genotypes. Transcriptome patterns suggest that JCRB0112.1 has diverged highly from the other three lines. RCB1189 and JCRB0112.1 responded to PMA faster than RCB3686 and JCRB0112. We have identified RCB3686 as the closest to the original THP-1, which can be an optimal model of AML-M5. These four THP-1 genomes and transcriptomes exhibit significant differences, indicating four independent sublines and demonstrating the influence of genetic drift on gene expression. As these cells share the same name, THP-1 must be accompanied by their registration number of each cell repository. Our data provide genomic features of four THP-1 sublines and serve as a reference profile to classify widely spread THP-1 progenies, which could be distinguished by a comparison of 24 STR markers. Multiple sublines can be generated by separate cell cultures, which would be explained by in vitro branched evolution.
THP-1 是一种代表性的白血病细胞系,在 JCRB 和 RIKEN BRC 细胞库中有四个不同的编号。然而,这四个细胞系之间的差异尚不清楚。在我们的研究中,对这四个 THP-1 细胞系 JCRB0112、JCRB0112.1(对应 ATCC TIB-202)、RCB1189(DSMZ ACC-16)和 RCB3686,在染色体和 DNA 序列水平上进行了比较。我们的结果表明,JCRB0112 和 RCB1189 的倍性发生了变化,分别为三倍体和四倍体。靶序列变异频率的模式是每个倍性所特有的,基于部分序列数据估计整个基因组状态。SNP 微阵列显示了四个不同的图谱,存在大规模的杂合性丢失,反映在 STR 基因型的细微差异上。转录组模式表明,JCRB0112.1 与其他三个细胞系的差异非常大。与 RCB3686 和 JCRB0112 相比,RCB1189 和 JCRB0112.1 对 PMA 的反应更快。我们已经确定 RCB3686 与原始 THP-1 最为接近,可以作为 AML-M5 的最佳模型。这四个 THP-1 基因组和转录组表现出显著差异,表明存在四个独立的亚系,并证明遗传漂变对基因表达的影响。由于这些细胞具有相同的名称,因此 THP-1 必须附有其每个细胞库的注册编号。我们的数据提供了四个 THP-1 亚系的基因组特征,作为分类广泛传播的 THP-1 后代的参考图谱,这些后代可以通过比较 24 个 STR 标记来区分。通过单独的细胞培养可以产生多个亚系,这可以通过体外分支进化来解释。