Signaling related with biphasic effects of bisphenol A (BPA) on Sertoli cell proliferation: A comparative proteomic analysis

被引:57
|
作者
Ge, Li-Chen [1 ]
Chen, Zhuo-Jia [2 ]
Liu, Hao [3 ,4 ]
Zhang, Kun-Shui [5 ]
Su, Qiao [6 ]
Ma, Xiang-Yu [1 ]
Huang, Hong-Bin [2 ]
Zhao, Zhen-Dong [7 ]
Wang, Yu-Ye [1 ]
Giesy, John P. [8 ,9 ]
Du, Jun [1 ]
Wang, Hong-Sheng [1 ]
机构
[1] Sun Yat Sen Univ, Sch Pharmaceut Sci, Dept Microbial & Biochem Pharm, Guangdong Prov Key Lab New Drug Design & Evaluat, Guangzhou 510006, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Ctr Canc, Collaborat Innovat Ctr Canc Med, Dept Pharm,State Key Lab Oncol South China, Guangzhou 510060, Guangdong, Peoples R China
[3] Guangzhou Med Univ, Canc Res Inst, Guangzhou 510095, Guangdong, Peoples R China
[4] Guangzhou Med Univ, Canc Hosp, Guangzhou 510095, Guangdong, Peoples R China
[5] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Dept Pharm, Guangzhou 510120, Guangdong, Peoples R China
[6] Sun Yat Sen Univ, Affiliated Hosp 1, Lab Anim Ctr, Guangzhou 510080, Guangdong, Peoples R China
[7] Guangdong Food & Drug Vocat Coll, Sch Chinese Mat Med, Guangzhou 510520, Guangdong, Peoples R China
[8] Univ Saskatchewan, Dept Vet Biomed Sci, Saskatoon, SK, Canada
[9] Univ Saskatchewan, Toxicol Ctr, Saskatoon, SK, Canada
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2014年 / 1840卷 / 09期
基金
中国国家自然科学基金;
关键词
Proteomics; Proliferation; TM4; cell; Oxidative stress; Energy metabolism; In vitro; COUPLED RECEPTOR 30; OXIDATIVE STRESS; CANCER-CELLS; EXPOSURE; MITOCHONDRIA; INDUCTION; METABOLISM; EXPRESSION; PROTECTS; GROWTH;
D O I
10.1016/j.bbagen.2014.05.018
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
Background: Biphasic effects on cell proliferation of bisphenol A (BPA) can occur at lesser or greater exposures. Sertoli cells play a pivotal role in supporting proliferation and differentiation of germ cells. The mechanisms responsible for inverse effects of great and low concentrations of BPA on Sertoli cell proliferation need further study. Methods: We utilized proteomic study to indentify the protein expression changes of Sertoli TM4 cells treated with 10(-8) M and 10(-5) M BPA. The further mechanisms related to mitochondria, energy metabolism and oxidative stress were investigated by ciRT-PCR and Western-blotting analysis. Results: Proteomic studies identified 36 proteins and two major clusters of proteins including energy metabolism and oxidative stress expressed with opposite changes in Sertoli cells treated with 10(-8) M and 10(-5) M BPA, respectively, for 24 h. Exposure to 10(-5) M BPA resulted in greater oxidative stress and then inhibited cell proliferation, while ROS scavenger NAC effectively blocked these effects. Exposure to 10(-8) M BPA caused higher intercellular ATP, greater activities of mitochondria, and resulted in significant proliferation of TM4 cells, while oligomycin A, an inhibitor of ATP synthase, abolished these growth advantages. Conclusions: Our study demonstrated that micromolar BPA inhibits proliferation of Sertoli cells by elevating oxidative stress while nanomolar BPA stimulates proliferation by promoting energy metabolism. General significance: Micromolar BPA inhibits cell proliferation by elevating oxidative stress while nanomolar BPA stimulates cell proliferation by promoting energy metabolism. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:2663 / 2673
页数:11
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