Related Experiment Video
Updated: Apr 25, 2026

Inducing and Characterizing Vesicular Steatosis in Differentiated HepaRG Cells
Published on: July 18, 2019
Stearoyl coenzyme A desaturase 1 is associated with hepatitis C virus replication complex and regulates viral
Lam N Nguyen1, Yun-Sook Lim1, Long V Pham1
1National Research Laboratory of Hepatitis C Virus and Ilsong Institute of Life Science, Hallym University, Anyang, South Korea.
Unlabelled:
The hepatitis C virus (HCV) life cycle is tightly regulated by lipid metabolism of host cells. In order to identify host factors involved in HCV propagation, we have recently screened a small interfering RNA (siRNA) library targeting host genes that control lipid metabolism and lipid droplet formation using cell culture-grown HCV (HCVcc)-infected cells. We selected and characterized the gene encoding stearoyl coenzyme A (CoA) desaturase 1 (SCD1). siRNA-mediated knockdown or pharmacological inhibition of SCD1 abrogated HCV replication in both subgenomic replicon and Jc1-infected cells, while exogenous supplementation of either oleate or palmitoleate, products of SCD1 activity, resurrected HCV replication in SCD1 knockdown cells. SCD1 was coimmunoprecipitated with HCV nonstructural proteins and colocalized with both double-stranded RNA (dsRNA) and HCV nonstructural proteins, indicating that SCD1 is associated with HCV replication complex. Moreover, SCD1 was fractionated and enriched with HCV nonstructural proteins at detergent-resistant membrane. Electron microscopy data showed that SCD1 is required for NS4B-mediated intracellular membrane rearrangement. These data further support the idea that SCD1 is associated with HCV replication complex and that its products may contribute to the proper formation and maintenance of membranous web structures in HCV replication complex. Collectively, these data suggest that manipulation of SCD1 activity may represent a novel host-targeted antiviral strategy for the treatment of HCV infection.
Importance:
Stearoyl coenzyme A (CoA) desaturase 1 (SCD1), a liver-specific enzyme, regulates hepatitis C virus (HCV) replication through its enzyme activity. HCV nonstructural proteins are associated with SCD1 at detergent-resistant membranes, and SCD1 is enriched on the lipid raft by HCV infection. Therein, SCD1 supports NS4B-mediated membrane rearrangement to provide a suitable microenvironment for HCV replication. We demonstrated that either genetic or chemical knockdown of SCD1 abrogated HCV replication in both replicon cells and HCV-infected cells. These findings provide novel mechanistic insights into the roles of SCD1 in HCV replication.
Insights
Stearoyl-CoA desaturase 1 (SCD1) is crucial for hepatitis C virus (HCV) replication. Inhibiting SCD1 blocks HCV, suggesting it’s a target for new antiviral therapies.
Area of Science:
- Virology
- Molecular Biology
- Biochemistry
Background:
- Hepatitis C virus (HCV) replication is influenced by host lipid metabolism.
- Identifying host factors is key to understanding HCV propagation.
Purpose of the Study:
- To identify host factors regulating HCV propagation.
- To characterize the role of stearoyl-CoA desaturase 1 (SCD1) in HCV replication.
Main Methods:
- Screened a siRNA library targeting lipid metabolism genes in HCV-infected cells.
- Utilized subgenomic replicons and Jc1-infected cells for experiments.
- Performed co-immunoprecipitation, fractionation, and electron microscopy.
Main Results:
- SCD1 knockdown or inhibition significantly reduced HCV replication.
- Supplementation with SCD1 products (oleate, palmitoleate) restored replication.
- SCD1 associates with HCV replication complexes and is essential for NS4B-mediated membrane rearrangement.
Conclusions:
- SCD1 is a critical host factor for HCV replication.
- SCD1 supports the formation of the membranous web required for HCV replication.
- Targeting SCD1 activity presents a potential host-directed antiviral strategy against HCV.
Related Concept Videos
Hepatitis
Viral Hepatitis I: Introduction
Lipid Catabolism
Cirrhosis II: Pathophysiology
Hepatic Drug Excretion: Influencing Factors
Viruses with RNA Genomes

