Effects of PDGFRα on melanocyte apoptosis induced by hydrogen perox-ide
10.3969/j.issn.1000-4718.2017.11.022
- VernacularTitle:血小板源性生长因子受体α影响过氧化氢诱导的黑素细胞凋亡
- Author:
Yong DENG
1
;
hui Ya JIANG
;
Yan WAN
;
rong He YANG
;
shui Chun YU
;
Juan HUANG
Author Information
1. 遂宁市中心医院皮肤科
- Keywords:
Melanocytes;
Platelet-derived growth factor receptor α;
Apoptosis;
Hydrogen peroxide
- From:
Chinese Journal of Pathophysiology
2017;33(11):2060-2066
- CountryChina
- Language:Chinese
-
Abstract:
AIM:To investigate the effects of platelet-derived growth factor receptor α(PDGFRα) on melano-cyte apoptosis induced by hydrogen peroxide(H2O2). METHODS:Melanocyte PIGI was used as the research object. Af-ter exposed to H2O2at different concentrations,the cell viability was detected by MTT assay. The PIGI cells were transfec-ted with empty vector pCMV6 or PDGFRα over-expression vector pCMV6-PDGFRα. The transfection efficiency was deter-mined by RT-qPCR and Western blot. The effect of H2O2on the viability of the PIGI cells after over-expression of PDGFRα was measured by MTT assay. The cell apoptosis was analyzed by flow cytometry. The protein levels of p38, p-p38 and cleaved caspase-3 in the cells were detected by Western blot. DCDHF-DA was used to estemate the generation of reactive oxygen species (ROS) in the cells. RESULTS:The viability of PIGI cells decreased after exposed to H2O2(P<0.05), and the half maximal inhibitory concentration of H2O2was 0.7 mmol/L. Transfection with PDGFRα over-expression vector successfully induced high expression of PDGFRα at mRNA and protein levels in the PIGI cells,and increased the viability of the cells with H2O2treatment(P<0.05). Over-expression of PDGFRα decreased the apoptotic rate of PIGI cells trea-ted with H2O2(P<0.05),and the level of ROS in the cells(P<0.05). The protein levels of cleaved caspase-3 and p-p38 were also decreased (P <0.05). CONCLUSION:PDGFRα inhibits the apoptosis of melanocytes induced by H2O2,partially reverses the growth inhibition of melanocytes by H2O2,and decreases the ROS level. The mechanism may be related to regulating the protein levels of p-p38 and cleaved caspase-3 in the cells.
