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Immortalized hepatocyte-like cells: A competent hepatocyte model for studying clinical HCV isolate infection.

Authors :
Pewkliang Y
Thongsri P
Suthivanich P
Thongbaiphet N
Keatkla J
Pasomsub E
Anurathapan U
Borwornpinyo S
Wongkajornsilp A
Hongeng S
Sa-Ngiamsuntorn K
Source :
PloS one [PLoS One] 2024 May 13; Vol. 19 (5), pp. e0303265. Date of Electronic Publication: 2024 May 13 (Print Publication: 2024).
Publication Year :
2024

Abstract

More than 58 million individuals worldwide are inflicted with chronic HCV. The disease carries a high risk of end stage liver disease, i.e., cirrhosis and hepatocellular carcinoma. Although direct-acting antiviral agents (DAAs) have revolutionized therapy, the emergence of drug-resistant strains has become a growing concern. Conventional cellular models, Huh7 and its derivatives were very permissive to only HCVcc (JFH-1), but not HCV clinical isolates. The lack of suitable host cells had hindered comprehensive research on patient-derived HCV. Here, we established a novel hepatocyte model for HCV culture to host clinically pan-genotype HCV strains. The immortalized hepatocyte-like cell line (imHC) derived from human mesenchymal stem cell carries HCV receptors and essential host factors. The imHC outperformed Huh7 as a host for HCV (JFH-1) and sustained the entire HCV life cycle of pan-genotypic clinical isolates. We analyzed the alteration of host markers (i.e., hepatic markers, cellular innate immune response, and cell apoptosis) in response to HCV infection. The imHC model uncovered the underlying mechanisms governing the action of IFN-α and the activation of sofosbuvir. The insights from HCV-cell culture model hold promise for understanding disease pathogenesis and novel anti-HCV development.<br />Competing Interests: The authors have declared that no competing interests exist.<br /> (Copyright: © 2024 Pewkliang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)

Details

Language :
English
ISSN :
1932-6203
Volume :
19
Issue :
5
Database :
MEDLINE
Journal :
PloS one
Publication Type :
Academic Journal
Accession number :
38739590
Full Text :
https://doi.org/10.1371/journal.pone.0303265