Regulation of hepatitis C virus core protein on the activity of signal transducers and activators of transcription 3.
- Author:
De-yun FENG
1
;
Bo LI
;
Hui ZHENG
;
Rui-xue CHENG
;
Ya CAO
Author Information
1. Department of Pathology, Basic Medical College, China. dyfeng743@sohu.com
- Publication Type:Journal Article
- MeSH:
Cell Line;
DNA-Binding Proteins;
metabolism;
Hepatocytes;
cytology;
metabolism;
Humans;
STAT3 Transcription Factor;
metabolism;
Signal Transduction;
Transfection;
Viral Core Proteins;
biosynthesis;
genetics
- From:
Journal of Central South University(Medical Sciences)
2005;30(6):631-635
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To investigate the regulation of hepatitis C virus (HCV) core protein on the activity of signal transducers and activators of transcription 3 (stat3).
METHODS:A cell line expressing stable HCV core protein-QSG7701-core was constructed by transfecting the pcDNA3. 1-core (expressing HCV core protein) into the human immortalized hepatocyte line QSG7701. The phosphorylation and DNA binding activity of stat3 were detected by immunocytochemistry, Western blot, and electrophoretic mobility shift assay (EMSA).
RESULTS:The expression level of phosphorylated stat3 in QSG7701-core cells was significantly lower than that in QSG7701-pcDNA3. 1 cells and untransfected QSG7701 cells, but there were no significant differences in the expression levels of total stat3 among the 3 groups. The positive signal of phosphorylated stat3 in nucleus of QSG7701-core cells was obviously weaker than that in QSG7701-pcDNA3. 1 cells and untransfected QSG7701 cells. EMSA showed that DNA binding activity of stat3 in QSG7701-core cells significantly decreased.
CONCLUSION:The expressionof HCV core protein in human hepatocyte line may suppress the phosphorylation and DNA binding activity of stat3, which may be one of the causes for resistance against interferon.
