Effects of bone marrow mesenchymal stem cell conditioned medium on bioactivity of scar fibroblasts
10.3969/j.issn.2095-4344.2014.07.005
- VernacularTitle:骨髓间充质干细胞条件培养液对瘢痕成纤维细胞生物活性的影响
- Author:
Yan WU
;
Chunlei ZHANG
;
Yang LIU
;
Hongzhi LI
;
Jing YU
;
Haihua BAO
;
Ran GUO
;
Xiaohuan YUAN
- Publication Type:Journal Article
- Keywords:
bone marrow;
mesenchymal stem cells;
culture media,conditioned;
cicatrix;
fibroblasts;
col agen type I;
col agen type III;
cellproliferation;
hydroxyproline
- From:
Chinese Journal of Tissue Engineering Research
2014;(7):1009-1014
- CountryChina
- Language:Chinese
-
Abstract:
BACKGROUND:Mesenchymal stem celltransplantation promoted skin repair in trauma via various regulatory mechanisms and inhibited scar formation. At present, many scholars believed that bioactive factors secreted by mesenchymal stem cells played an important role.
OBJECTIVE:To investigate the effects of bone marrow mesenchymal stem cellconditioned medium on the proliferation and col agen synthesis of hypertrophic scar fibroblasts.
METHODS:Human bone marrow mesenchymal stem cells and hypertrophic scar fibroblasts were isolated and cultured, and bone marrow mesenchymal stem cellconditioned medium was prepared. Hypertrophic scar fibroblasts were cultured in vitro with 12, 24, and 48 hour-col ected conditioned medium for 24 hours, which was compared with blank control group. The proliferation of cells was determined by CCK-8. Type I and type III col agen expression in hypertrophic scar fibroblasts was detected using real-time PCR.
RESULTS AND CONCLUSION:Compared with the blank control group, 24 and 48 hour-col ected conditioned medium significantly inhibited the proliferation of hypertrophic scar fibroblasts (P<0.01), and also suppressed col agen synthesis of hypertrophic scar fibroblasts (P<0.01). Results suggested that bone marrow mesenchymal stem cellconditioned medium inhibited the proliferation and col agen synthesis of hypertrophic scar fibroblasts by secreting anti-fibrotic bioactive factors, which may provide new theoretical supports for celltherapy to reduce cutaneous scarring.
