Inhibition of hepatocyte growth factor on proliferation and transdifferentiation of human Tenon capsule fibroblasts triggered by transforming growth factor-β1 in vitro
10.3760/cma.j.issn.2095.0160.2018.12.006
- VernacularTitle:肝细胞生长因子对转化生长因子-β1诱导的人Tenon囊成纤维细胞增生及转分化的抑制作用
- Author:
Jing CHEN
1
;
Yong WANG
;
Donghao LI
Author Information
1. 510150,广州医科大学附属第三医院眼科
- Keywords:
Tenon capsule/cytology;
Fibroblasts/metabolism;
Hepatocyte growth factor/administration &dosage;
Transforming growth factor beta type 1;
Fibrosis/prevention & control;
α.Smooth muscular actin;
Humans;
Cells,cultured
- From:
Chinese Journal of Experimental Ophthalmology
2018;36(12):925-930
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the effects of hepatocyte growth factor ( HGF ) on proliferation and transdifferentiation of human Tenon capsule fibroblasts induced by transforming growth factor .β1(TGF.β1) in vitro. Methods Human Tenon capsule fibroblasts were cultured and divided into blank control group, TGF.β1 treated group and different concentrations HGF+TGF.β1 groups. The TGF.β1 at 10 μg/L was added into culture medium of the TGF.β1 treated group,and different concentrations of HGF (25,50,100,200 μg/L) and 10μg/L TGF.β1 were added into culture medium of the HGF25μg/L+TGF.β1 ,HGF50μg/L+TGF.β1 ,HGF100μg/L+TGF.β1 ,HGF200μg/L+TGF.β1 group respectively,Methyl thiazolyl tetrazolium ( MTT) was employed to measure the cell proliferation ( absorbance at 560 nm) . Immunofluorescence staining was used to evaluate and locate the expression of α.smooth muscle action (α.SMA) in the cells. The expression ofα.SMA protein in the cells was detected by Western blot assay. Results Cultured cells showed fusiform in shape with the positive response for vimentin. The proliferation value of the cells was 0. 203±0. 025,0. 497±0. 101,0. 426±0. 062,0. 354±0. 040,0. 272±0. 084,0. 241±0. 011 in the blank control group, TGF.β1 treated group,HGF25μg/L+TGF.β1 group,HGF50μg/L+TGF.β1 group,HGF100μg/L+TGF.β1 group and HGF200μg/L+TGF.β1 group,respectively,showing a significant difference among the groups (F=9. 210,P=0. 003). Compared with the TGF.β1 treated group,the proliferation values of the cells were significantly reduced in the blank control group and HGF+TGF.β1 group ( all at P<0. 05 ) . Immunofluorescence staining showed that α.SMA protein mainly located in cytoplasm with the strong red fluorescence in the cells of the TGF.β1 treated group and weak red fluorescence in HGF+TGF.β1 group,and the expression of α.SMA was absent in the blank control group. The percentage of α.SMA.positive cells was ( 60. 0 ± 4. 7 )％ in the TGF.β1 treated group and ( 14. 3 ± 3. 1 )％ in the HGF+TGF.β1 group, with significant difference between the two groups (t=19. 856,P<0. 001). The relative expression levels of the α.SMA protein in the cells were 0. 642±0. 032,1. 330±0. 069 and 0. 884±0. 040 in the blank control group,TGF.β1 group and HGF100μg/L+TGF.β1 group, respectively, showing a significant difference among the groups ( F=13. 370, P<0. 001),and relative expression levels of the α.SMA protein in the cells were significantly lower in the blank control group and HGF100μg/L+TGF.β1 group than that in the TGF.β1 treated group (all at P<0. 05). Conclusions HGF can inhibit the proliferation of human Tenon capsule fibroblasts, down.regulate the expression of α.SMA protein induced by TGF.β1 and arrest the phenotype transformation of fibroblasts in vitro.
