Asian Science Citation Index is committed to provide an authoritative, trusted and significant information by the coverage of the most important and influential journals to meet the needs of the global scientific community.  
ASCI Database
308-Lasani Town,
Sargodha Road,
Faisalabad, Pakistan
Fax: +92-41-8815544
Contact Via Web
Suggest a Journal
 
Articles by F. Liu
Total Records ( 5 ) for F. Liu
  F. Liu , J. Fei , N. Li and Q. Meng
  Muscle regeneration recapitulates myogenesis. HGF (hepatocyte growth factor) plays an important role in muscle development, as the only secreted growth factor, which can activates myoblasts proliferation. The expression units of wild HGF promoter-luciferase vector exceeded the expression units of HGF promoter-luciferase vector with mutated binding sequence of MyoD, also the expression trend of HGF was in accordance with the expression of MyoD. The expression of MyoD directly affects the expression of HGF during muscle development. In C2C12 culture, the expression of HGF is up-regulated in the phase of proliferation process, but down-related in the phase of differentiation. We identified the proliferation and differentiation stage of C2C12 culture by the definition of expression of myogenic regulator family (MyoD, yf5, yogenin, Myf6) and detected the HGF level during this two stages. MyoD bind site was found in the 5’-UTR of HGF promoter. MyoD is b HLH (basic helix-loop-helix) transcriptional activator which has a critical role during myogenesis. We verified that MyoD can bind the active b HLH site, as shown by EMSA. Transfection of wild HGF promoter-luciferase eukaryotic expression vector with MyoD binding site and HGF promoter-luciferase eukaryotic expression vector with mutated MyoD binding site into C2C12 myoblasts was done.
  H. Liu , G. Li , W. Zhong , D. Li , F. Liu and W. Sun
  Essential amino acids, particularly those containing the element sulfur, are required by small canids to produce a high quality pelt. The experiments were designed to estimate the effect of a diet supplemented with the sulfur-containing amino acid methionine on the nutrient metabolism and pelt quality of raccoon dogs (Nyctereutes procyonoides). Seventy-five male raccoon dogs with similar body weights were randomly assigned to five dietary groups of 15 each during the winter fur growth period. The diet for the control group contained 24% protein while the diets for groups 1 to 4 contained 20% protein plus 0.15, 0.35, 0.55 and 0.75 g methionine per 100 g dry matter, respectively, for a 60-day period. As a result, the body weights in group 4 were clearly reduced compared to the other groups (p<0.05). Dry matter intake in the control group was significantly higher than for groups 1 and 2 (p<0.05), but was similar to groups 3 and 4. Although, serum methionine level was similar among all groups, group 2 showed significantly higher total protein in serum (p<0.05) than the control group; while serum urea nitrogen in group 2 was lower than that of groups 3 or 4 (p<0.05). The pelt length in the control group and in group 2 was significantly longer than the other groups. The density of guard hair and fiber in the controls and groups 1 and 2 was remarkably higher compared with that in groups 3 and 4 (p<0.05). These results suggest that a certain amount of supplemental methionine may reduce the total protein requirement in the diet without affecting the pelt quality of raccoon dogs.
  Y. N Yang , X. L Wang , Y. T Ma , X Xie , Z. Y Fu , X. M Li , B. D Chen and F. Liu
 

Objectives: Cytochrome P450 (CYP) 2C19 is expressed in vascular endothelium and metabolizes arachidonic acid to biologically active epoxyeicosatrienoic acids (EETs), which are potent endogenous vasodilators and inhibitors of vascular inflammation. The purpose of this study is to explore the relationship between the interaction of CYP2C19*3 polymorphism and smoking and coronary artery disease (CAD) in a Uighur population. Methods: In a Chinese Uighur case-control study of patients with CAD (n = 336) and healthy controls (n = 370), we investigated the roles of polymorphism in the CYP2C19 gene by the use of polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) analysis. Results: The CYP2C19*3 AG + AA genotype was significantly more prevalent in patients with CAD (6.25.0% vs 2.96%; P = .03). Multiple logistic regression analysis showed 4 independent risk factors: the interaction of CYP2C19*3 and smoking (OR 7.22, 95% confidence interval [CI] 2.32-10.23; P = .009), smoking (OR 3.23, 95% CI 1.72-5.44; P = .003), blood sugar (OR 2.12, 95% CI 1.03-4.21; P < .01), and hypertension (OR 1.74, 95% CI 0.98-2.34; P = .013). Conclusions: The CYP2C19*3 polymorphism and CAD were synergistically and significantly associated in Chinese Uighur patients.

  Q. Fang , S. Chen , Y. Wang , S. Jiang , R. Zhang , C. Hu , C. Wang , F. Liu , K. Xiang and W. Jia
  Aims  Hepatocyte nuclear factor-1α (HNF-1α) regulates the expression of genes encoding proteins involved in glucose metabolism and insulin secretion. Mutations in the HNF-1α gene cause maturity-onset diabetes of the young Type 3. However, the mechanism leading to this disease has not been completely ascertained. Previously, we found a novel mutation in the regulatory element of the human HNF-1α gene in two Chinese diabetes pedigrees. The nucleotide at position -128 T was substituted by G (nt-128 T[RIGHTWARDS ARROW]G). In this study, we analysed the functional defect of nt-128 T[RIGHTWARDS ARROW]G in HNF-1α transcription activity.

Methods  Luciferase reporter gene assays were carried out to examine the functional characteristics of this mutant. Electrophoretic mobility shift assays and chromatin immunoprecipitation were performed to confirm the binding of nuclear proteins to oligonucleotides.

Results  The variant construct (nt-128 T[RIGHTWARDS ARROW]G) had a 1.65-fold increase in promoter activity compared with that of the wild-type construct in HepG2 cells and a 1.33-fold increase in MIN6 cells, respectively. The variant resided at a FOXA/HNF-3 binding site identified by a series of competitive electrophoretic mobility shift assays and antibody supershift analyses. The assays showed a differential binding affinity in the wild-type and the nt-128 T[RIGHTWARDS ARROW]G mutant fragments by FOXA/HNF-3. Chromatin immunoprecipitation indicated that FOXA/HNF-3 bound to this region in vivo. One nucleotide substitution in the FOXA/HNF-3 site in the human HNF-1α regulatory element caused an increase of HNF-1α transcriptional activity.

Conclusions  Our data suggested that this substitution in the promoter region affects DNA-protein interaction and HNF-1α gene transcription. The mutant may contribute to the development of diabetes in these two nt-128 T[RIGHTWARDS ARROW]G pedigrees of Chinese.

  C. Ju , B. Xu , Y. Lu , X.J. Mo , T. Zhang , S.B Chen , F. Liu , S.J. Cui , W. Liu , J.H. Chen , Z. Feng , J.X. Peng and W. Hu
  Schistosomiasis ranks as the second most serious parasitic disease worldwide after malaria. More than 250 million people are infected with schistosomes in the tropics or subtropics. The treatment and control of schistosomiasis which is a major neglected tropical parasitic disease, depends almost exclusively on chemotherapy with Praziquantel (PZQ). Current serologic diagnostic assays have shown that schistosome specific antibodies in human serum may remain for at least 1 year after cure. Repeated administration of PZQ for a long time might induce drug resistance to the parasite which is a big challenge for strategizing for the prevention and control of schistosomiasis. As schistosome eggs represent the most pathogenic form causing the disease, it is essential to determine if and how the level of antibodies against schistosome Soluble Egg Antigens (SEA) is affected by PZQ treatment. In this study, researchers carried out an immunomic analysis to profile Schistosoma japonicum SEA reacting with pooled human serum samples of pre and post treatment with PZQ by two dimensional electrophoresis combined with Western blotting. A total of 67 protein spots that were serologically recognized by serum samples were successfully subjected to mass spectrometric analysis. Of them, 37 different characterized proteins were successfully identified. Furthermore, of 67 protein spots, the reactivity of 49 protein spots to sera was reduced 20 weeks after PZQ treatment whereas only 5 spots showed increases in the intensity of recognition by post treatment sera. The present study suggested that chemotherapy with PZQ mainly affects the intensity of serological recognition of S. japonicum SEA. The immunomic proteins that were identified may facilitate a better understanding of the egg induced pathogenesis of schistosomiasis and host-parasite interplay and may provide potential targets for the diagnosis and evaluation of treatment for the disease as well.
 
 
 
Copyright   |   Desclaimer   |    Privacy Policy   |   Browsers   |   Accessibility