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ID: 1041 Effectiveness of human adipose-derived stem cell therapy pretreated with hepatocyte growth factor in liver fibrosis mouse model
- Source :
- Biomedical Research and Therapy. 4:119
- Publication Year :
- 2017
- Publisher :
- Biomedical Research and Therapy, 2017.
-
Abstract
- Background: Adipose-derived stem cells (ADSCs) have the potential therapeutic impact on the liver fibrosis. Hepatocyte growth factor (HGF) is pivotal for damage repair with its anti-apoptotic, anti-fibrotic and cell migration-promoting effect. In this study, the therapy with HGF-pretreated hADSCs was expected to enhance the therapeutic effect in the amelioration of liver fibrosis compared with untreated hADSCs. Method: HGF-hADSCs were prepared by culturing hADSCs for seven days in the medium added HGF. HGF-hADSCs transplantation was performed to investigate the therapeutic effect of these cells on carbon tetrachloride (CCl4)-induced liver fibrosis in a mouse model. Results: After seven days and fourteen days of cell transfusion, HGF-hADSCs ameliorated the liver fibrosis. The results showed the attenuation of the liver injury (ALT level), the down-regulation of procollagen-1 (7 days, 3-fold; 14 days, 6.7-fold) and alpha -smooth muscle actin (alpha-SMA) expression (7 days, 10-fold; 14 days, 2-fold), and the histological improvement. Notably, there was the significant difference in the procollagen-1 between HGF-hADSCs and untreated hADSCs groups. Thus, the therapy with HGF-hADSCs was more efficient in the liver fibrosis treatment compared with untreated hADSCs. Conclusion: HGF pretreated hADSCs have a potential therapy in the treatment of liver fibrosis
- Subjects :
- Liver injury
Pathology
medicine.medical_specialty
business.industry
Mesenchymal stem cell
Adipose tissue
Pharmacology
medicine.disease
General Biochemistry, Genetics and Molecular Biology
Cell therapy
Transplantation
Liver disease
medicine
Hepatocyte growth factor
Stem cell
business
medicine.drug
Subjects
Details
- ISSN :
- 21984093
- Volume :
- 4
- Database :
- OpenAIRE
- Journal :
- Biomedical Research and Therapy
- Accession number :
- edsair.doi...........7c53752b8a4aac48495b66d908e729f8
- Full Text :
- https://doi.org/10.15419/bmrat.v4is.317