关键词: 人凝血因子Ⅷ, L-精氨酸, 一氧化氮信号通路, 磷酸化

Abstract:

Abstract:Objective  To set up the molecular cytobiological model of  endogenous coagulation factor Ⅷ (FⅧ) re-expressing in human liver cells L02, and to study the regulation pathway and molecular basis of the re-expression of FⅧ in L02 cells activated by NO signal.Methods The L02 cells at logarithm growth phase were selected and randomly divided into blank control group and experimental group,inhibitor group and  inhibitor control group;they were cultured for 0,12,24,36,48, and 60 h.Flow cytometry was used to detect the expression of human FⅧ protein in L02 cells after treated for 48 h.Griess experiment was performed  to detect the levels of NO in L02 cells at different time points;the transcription levels of human FⅧ gene,iNOS gene,NF-κB1 gene and I-κB alpha gene were detected by RT-PCR method.Western blotting method was used to detect the expression levels of human phosphorylated I-kappaB (phosphorylated I-κB)  in L02 cells.Results The results of flow cytometry showed that the expression of human L02 FⅧ protein was found after treated with L-arginine for 48 h.The Griess results showed that the levels of NO in L02 cells in experimental group were significantly increased at 3,6,12, and 24 h（P<0.05） and the levels of NO in blank control group,inhibitor group and  inhibitor control group had no changes.The RT-PCR results showed that the transcription of human FⅧ mRNA in L02 cells was found in experimental group,but there was no transcription of human FⅧ mRNA in blank control group,inhibitor group and  inhibitor control group;the transcription levels of iNOS,NF-κB1 and I-κB alphain experiment group were increased（P<0.05） and the transcription levels of these genes in blank control group,inhibitor group and  inhibitor control group had no changes.The Western blotting results showed that after adding L-arginine the expression level of phosphorylated I-κB was significantly increased（P<0.05）,other groups had no such change.Conclusion L-arginine can activate the phosphorylation of I-κB by NO signal pathway to lead to the changes in the expression of human FⅧ gene promoter upstream regulatory-related transcription factors NF-κB to activate the expression of human FⅧ in human liver cells L02.

Key words:  , human coagulation factor Ⅷ, L-arginine, Nitrogen monoxide signal pathway, phosphorylation