Mangiferin protects osteoblast against oxidative damage by modulation of ERK5/Nrf2 signaling

被引:35
作者
Xia, Gen [1 ]
Li, Xueru [2 ]
Zhu, Xi [1 ]
Yin, Xueming [3 ]
Ding, Huiqiang [1 ]
Qiao, Yongdong [1 ]
机构
[1] Ningxia Med Univ, Gen Hosp, Dept Orthoped, 804 South Shengli St, Yinchuan 750000, Peoples R China
[2] Ningxia Med Univ, Gen Hosp, Dept Ultrasound, Cardiovasc Dis & Cerebrovasc Dis Hosp, Yinchuan, Peoples R China
[3] Third Peoples Hosp Ningxia, Dept Gen Surg, Yinchuan, Peoples R China
关键词
MAN; Osteoblast; Oxidative damage; ERK5; Nrf2; APOPTOTIC CELL-DEATH; EXTRACT VIMANG; STRESS; OSTEOPOROSIS; ALENDRONATE; ACTIVATION; AUTOPHAGY; DIAGNOSIS; PATHWAY; MODEL;
D O I
10.1016/j.bbrc.2017.06.184
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Oxidative stress has currently been proposed as a risk factor associated with the development and proression of osteoporosis. In this study, we identify the effect of mangiferin (MAN) on apoptosis and differentiation of osteoblast-like MC3T3-E1 cells insulted by H2O2. We firstly found that MAN can promote cell proliferation of MC3T3-E1 cells in a time-and dose-dependent manner and stimulate the phosphorylation of ERK5. Cells were divided as five groups: control, H2O2 (100 mu M, control), H2O2 + MAN (5 mu M), H2O2 + MAN (10 mu M), and H2O2 + MAN (20 mu M). MAN can significantly decrease H2O2-induced apoptosis and elevated ROS level of MC3T3-E1 cells. The expressions of caspase-3, caspase-9 and Bax/Bcl-2 were increased with H2O2 treatment, and MAN can reverse these changes. In addition, Nrf2 and its downstream target effectors (Hal, NQO1) were dramatically attenuated in MC3T3-E cells treatment with H2O2, while MAN can significantly increase the expression of Nrf2, HO1 and NQO1. The expression of ERK5 was down regulated by RNA interference in MOT3-E1 cells, and we found that MAN (20 mu M) pretreatment didn't make remarkable decrease in cell apoptosis or expressions of apoptosis-related proteins in H2O2-insulted siRNA-ERK5 cells. This study indicated that MAN can protect osteoblast against oxidative damage by modulation of ERK5/Nrf2 signaling, which can be new agent for osteoporosis. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:807 / 813
页数:7
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