4-Nonylphenol induces autophagy and attenuates mTORp70S6K/4EBP1 signaling by modulating AMPK activation in Sertoli cells

被引:61
作者
Duan, Peng [1 ,2 ]
Hu, Chunhui [3 ]
Quan, Chao [1 ]
Yu, Tingting [1 ]
Huang, Wenting [1 ]
Chen, Wei [1 ]
Tang, Sha [1 ]
Shi, Yuqin [4 ]
Martin, Francis L. [5 ]
Yang, Kedi [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Dept Occupat & Environm Hlth, Key Lab Environm & Hlth,MOE Minist Educ, Wuhan 430030, Peoples R China
[2] Hubei Univ Med, Res Ctr Environm & Hlth, Shiyan 442000, Peoples R China
[3] Hubei Univ Med, Taihe Hosp, Dept Clin Labs, Shiyan 442000, Peoples R China
[4] Wuhan Univ Sci & Technol, Coll Med, Sch Publ Hlth, Dept Epidemiol & Hlth Stat, Wuhan 430030, Peoples R China
[5] Univ Cent Lancashire, Sch Pharm & Biomed Sci, Preston PR1 2HE, Lancs, England
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
4-nonylphenol; Sertoli cells; Autophagy; AMPK; mTOR-p70S6K/EBP1; INDUCED APOPTOSIS; MAMMALIAN TARGET; STEM-CELLS; MALE RATS; NONYLPHENOL; EXPOSURE; SPERMATOGENESIS; RAPAMYCIN; PATHWAYS; MTOR;
D O I
10.1016/j.toxlet.2016.12.015
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The estrogenic chemical 4-nonylphenol (NP) is known to impair testicular devolopment and spermatogenesis in rodents. The objective of this study was to explore the effects of NP on autophagy induction and AMPK-mTOR signaling pathway in Sertoli cells (SCs), which are the "nursemaid cells" for meiosis of spermatocytes. In this study we exposed 7-week-old male rats to NP by intra-peritoneal injection at 0, 20, 50 or 100 mg/kg body weight/2 days for 20 consecutive days. Our results showed that exposure to NP dose-dependently induces the formation of autophagosomes in SCs, increases the expression of Beclin-1, the conversion of LC3-I to LC3-II and the mRNA expression of Atg3, Atg5, Atg7 and Atg12 in testis, and these effects are concomitant with the activation of AMPK, and the suppression of TSC2-mTOR-p70S6K/4EBP1 signaling cascade in testis. Furthermore, 10 mu M Compound C or AMPI kappa alpha l siRNA pre-treatment effectively attenuated autophagy and reversed AMPK-mTOR-p70S6K/4EBP1 signaling in NP-treated SCs. Co-treatment with 1 mM AICAR remarkably strengthened NP-induced autophagy and mTOR inhibition in SCs. Together, these data suggest that NP stimulates Sertoli cell autophagy and inhibits mTOR-p70S6KRIEBP1 activity through AMPK activation, which is the potential mechanism responsible for the regulation of testis function and differentiation following NP exposure. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:21 / 31
页数:11
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