Transfection of single-stranded hepatitis A virus RNA activates MHC class I pathway
Authors: SUZUKI, K.1; YANAGI, M.2; MORI-AOKI, A.1; MORIYAMA, E.1; ISHII, K. J.3; KOHN, L. D.1
Source: Clinical & Experimental Immunology, Volume 127, Number 2, February 2002 , pp. 234-242(9)
Publisher: Blackwell Publishing
Abstract:
SUMMARY Although infection of single-stranded RNA viruses can enhance expression of major histocompatibility complex (MHC) class I genes, the mechanism underlying this process remains unclear. Recent studies have indicated that exposure of non-immune cells to double-stranded deoxyribonucleic acid (DNA) or ribonucleic acid (RNA) of viral origin can directly increase the expression of MHC class I and related molecules without immune cell interaction. In this report, we show that transfection of single-stranded hepatitis A virus RNA into cultured hepatocytes results in the induction of genes for MHC class I, LMP2 and transporter for antigen processing (TAP1), in addition to the generation of viral proteins. We suggest that this stimulatory effect is due to the double-stranded RNA formed during replication of single-stranded viral RNA, and involves both double-stranded, RNA-dependent protein kinase PKR and the secretion of IFNβ.Keywords: infectious immunity-virus; MHC; antigen presentation; protein kinases/phosphatases
Document Type: Research article
DOI: 10.1046/j.1365-2249.2002.01767.x
Affiliations: 1: Cell Regulation Section, Metabolic Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Maryland, USA, 2: Department of Internal Medicine, Kanazawa University School of Medicine, Ishikawa, Japan, 3: Section of Retroviral Immunology, Center for Biologics, Evaluation, and Research, Food and Drug Administration, Maryland, USA, and

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