Institute of Biomedical Chemistry, 119121 Moscow, Russia.
Int J Mol Sci. 2023 May 15;24(10):8791. doi: 10.3390/ijms24108791.
Comparative transcriptomic analysis is a powerful approach for investigating the molecular mechanisms underlying various physiological and pathological processes, including liver disease. The liver is a vital organ with diverse functions, including metabolism and detoxification. In vitro models of liver cells, such as HepG2, Huh7, and Hep3B, have been widely used to study liver biology and pathology. However, there is limited information on the heterogeneity of these cell lines at the transcriptomic level.
This study aimed to conduct a comparative transcriptomic analysis of three common liver cell lines (HepG2, Huh7, and Hep3B) using publicly available RNA-sequencing data. In addition, we compared these cell lines to primary hepatocytes, cells isolated directly from liver tissue and considered the gold standard for studying liver function and disease.
Our study included sequencing data with the following criteria: total number of reads over 20,000,000, average read length of over 60 base pairs, Illumina sequencing, and non-treated cells. The data for the three cell lines were compiled: HepG2 (97 samples), Huh7 (39 samples), and Hep3B (16 samples). We performed differential gene expression analysis using the DESeq2 package, principal component analysis, hierarchical clustering on principal components, and correlation analysis to explore the heterogeneity within each cell line.
We identified numerous genes and pathways differentially expressed between HepG2, Huh7, and Hep3B, such as oxidative phosphorylation, cholesterol metabolism, and DNA damage. We report that the expression levels of important genes differ significantly between primary hepatocytes and liver cell lines.
Our study provides new insights into the transcriptional heterogeneity of commonly used liver cell lines and highlights the importance of considering specific cell line. Consequently, transferring results without considering the heterogeneity of cell lines is impractical and may lead to inaccurate or distorted conclusions.
比较转录组分析是研究各种生理和病理过程(包括肝脏疾病)分子机制的有力方法。肝脏是一个具有多种功能的重要器官,包括代谢和解毒。HepG2、Huh7 和 Hep3B 等肝细胞体外模型已广泛用于研究肝脏生物学和病理学。然而,关于这些细胞系在转录组水平上的异质性信息有限。
本研究旨在使用公开的 RNA-seq 数据对三种常见的肝细胞系(HepG2、Huh7 和 Hep3B)进行比较转录组分析。此外,我们将这些细胞系与原代肝细胞进行比较,原代肝细胞是直接从肝组织中分离出来的细胞,被认为是研究肝脏功能和疾病的金标准。
我们的研究包括符合以下标准的测序数据:总读取数超过 2000 万,平均读长超过 60 个碱基,Illumina 测序,以及未经处理的细胞。将 HepG2(97 个样本)、Huh7(39 个样本)和 Hep3B(16 个样本)三种细胞系的数据进行编译。我们使用 DESeq2 包进行差异基因表达分析,进行主成分分析、主成分层次聚类和相关性分析,以探索每个细胞系内的异质性。
我们鉴定出许多在 HepG2、Huh7 和 Hep3B 之间差异表达的基因和途径,如氧化磷酸化、胆固醇代谢和 DNA 损伤。我们报告称,重要基因在原代肝细胞和肝细胞系之间的表达水平存在显著差异。
我们的研究为常用的肝细胞系的转录组异质性提供了新的见解,并强调了考虑特定细胞系的重要性。因此,不考虑细胞系异质性而转移结果是不切实际的,并且可能导致不准确或扭曲的结论。