ULBP1 is induced by hepatitis C virus infection and is the target of the NK cell-mediated innate immune response in human hepatocytes.
Hiromichi DansakoHirotaka ImaiYouki UedaShinya SatohTakaji WakitaNobuyuki KatoPublished in: FEBS open bio (2018)
Natural killer (NK) cells through their NK group 2 member D (NKG2D) receptors recognize NKG2D ligands such as UL16-binding proteins (ULBPs) on virus-infected cells and subsequently trigger the host innate immune response. In the present study, we demonstrated that hepatitis C virus (HCV) induced the cell surface expression of ULBP1 in human immortalized hepatocyte PH5CH8 cells and human hepatoma HuH-7 cell-derived RSc cells. Interestingly, NK cell line NK-92 induced cytotoxicity and interferon-γ mRNA expression and subsequently reduced the levels of HCV RNA replication during co-culture with HCV-infected RSc cells. From these results, we conclude that ULBP1 is a target of the NK cell-mediated innate immune response in HCV-infected human hepatocytes.
Keyphrases
- nk cells
- immune response
- hepatitis c virus
- endothelial cells
- induced apoptosis
- human immunodeficiency virus
- high glucose
- dendritic cells
- induced pluripotent stem cells
- cell cycle arrest
- pluripotent stem cells
- toll like receptor
- liver injury
- signaling pathway
- drug induced
- poor prognosis
- cell surface
- diabetic rats
- oxidative stress
- ionic liquid