Human hepatic cell line 5: In-vitro model for hepatic immunobiology.
1/5 보강
[BACKGROUND] Hepatocellular carcinoma (HCC) remains a major global health burden, partly due to the lack of physiologically relevant in vitro models that accurately recapitulate early host-virus inter
APA
Shrestha S, Yeong MY, et al. (2026). Human hepatic cell line 5: In-vitro model for hepatic immunobiology.. Molecular biology reports, 53(1), 350. https://doi.org/10.1007/s11033-026-11502-w
MLA
Shrestha S, et al.. "Human hepatic cell line 5: In-vitro model for hepatic immunobiology.." Molecular biology reports, vol. 53, no. 1, 2026, pp. 350.
PMID
41632415
Abstract
[BACKGROUND] Hepatocellular carcinoma (HCC) remains a major global health burden, partly due to the lack of physiologically relevant in vitro models that accurately recapitulate early host-virus interactions and immune responses. Human Hepatocyte Line 5 (HHL-5) is an immortalized hepatocyte cell line that retains key liver-specific functions. This study aimed to characterize the phenotypic, genetic, and metabolic features of HHL-5 cells and evaluate their suitability as a non-cancerous hepatic model, in comparison with the HCC cell line HepG2.
[METHODS AND RESULTS] Morphological and phenotypic assessment of cells showed smaller cell and nuclear areas and slower proliferation with markedly longer doubling time of HHL-5 cells than HepG2 cells. Genomic analyses using whole-exome sequencing revealed enrichment of immune-related pathways in HHL-5 cells, including antigen processing and presentation, whereas HepG2 cells showed predominance of DNA replication pathways. Metabolomic profiling of cells by nuclear magnetic resonance spectroscopy showed hepatocyte-like oxidative profiles of HHL-5 cells, in contrast to the glycolytic phenotypes of HepG2 cells. Moreover, Western blotting for selected proteins showed reduced expression of oncogenic and stress-response markers, including c-Myc, pSTAT3, pNrf2, and select cytochrome P450 enzymes.
[CONCLUSION] Our findings support HHL-5 cells as a robust non-cancerous in vitro model for investigating liver diseases, viral infection, and early events in hepatocarcinogenesis.
[CLINICAL TRIAL REGISTRATION] Not applicable.
[METHODS AND RESULTS] Morphological and phenotypic assessment of cells showed smaller cell and nuclear areas and slower proliferation with markedly longer doubling time of HHL-5 cells than HepG2 cells. Genomic analyses using whole-exome sequencing revealed enrichment of immune-related pathways in HHL-5 cells, including antigen processing and presentation, whereas HepG2 cells showed predominance of DNA replication pathways. Metabolomic profiling of cells by nuclear magnetic resonance spectroscopy showed hepatocyte-like oxidative profiles of HHL-5 cells, in contrast to the glycolytic phenotypes of HepG2 cells. Moreover, Western blotting for selected proteins showed reduced expression of oncogenic and stress-response markers, including c-Myc, pSTAT3, pNrf2, and select cytochrome P450 enzymes.
[CONCLUSION] Our findings support HHL-5 cells as a robust non-cancerous in vitro model for investigating liver diseases, viral infection, and early events in hepatocarcinogenesis.
[CLINICAL TRIAL REGISTRATION] Not applicable.
MeSH Terms
Humans; Hepatocytes; Hep G2 Cells; Liver Neoplasms; Liver; Carcinoma, Hepatocellular; Cell Proliferation; Cell Line