Hydrogen peroxide accelerates senescence of human dental pulp stem cells
10.3969/j.issn.2095-4344.2016.10.016
- VernacularTitle:过氧化氢刺激人牙髓干细胞的衰老进程
- Author:
Ke XU
;
Guijuan FENG
;
Xingmei FENG
;
Dan HUANG
;
Ke ZHENG
;
Enyi TANG
- Publication Type:Journal Article
- Keywords:
Dental Pulp;
Stem Cels;
Hydrogen Peroxide;
Cel Aging;
Tissue Engineering
- From:
Chinese Journal of Tissue Engineering Research
2016;20(10):1481-1487
- CountryChina
- Language:Chinese
-
Abstract:
BACKGROUND:The process of oxidative stress that impacts the curative effect exists in the region which accepts cel transplantation. However, there are few reports about the effects of oxidative stress on human dental pulp stem cels and relevant mechanism.
OBJECTIVE:To understand the effect of hydrogen peroxide on the senescence of human dental pulp stem cels.
METHODS:Human dental pulp stem cels were isolated and cultured in PBS, 100 and 200 μmol/L hydrogen peroxide for 2 hours, respectively. Cel morphology was observed under inverted microscope, degree of cel senescence monitored by β-galactosidase staining, cel proliferation ability detected by BrdU kit and cel counting method, cytoskeleton of dental pulp stem cels and expression of sirt1 tested using immunofluorescence method, and expression of sirt1 and p16 proteins measured by western blot assay.
RESULTS AND CONCLUSION:Dental pulp stem cels exhibited a fibroblast-like morphology with spindle-shaped appearance. After stimulated by hydrogen peroxide, the cel volume was enlarged, theβ-galactosidase staining deepened and the proliferation of dental pulp stem cels reduced. The enhancement of senescence of dental pulp stem cels was accompanied with the increasing concentration of hydrogen peroxide, and in this process, the expression of p16 was raised while the expression of sirt1 was decreased. In conclusion, the senescence of human dental pulp stem cels can be promoted by the stimulation of hydrogen peroxide, and sirt1 and p16 are involved in this process. Our findings may provide a theoretical and experimental foundation for autologous transplantation of dental pulp stem cels.
