Decreased spermatogenesis led to alterations of testis-specific gene expression in male mice following nano-TiO2 exposure

被引:57
|
作者
Hong, Fashui [1 ,3 ]
Zhao, Xiaoyang [2 ,4 ]
Si, Wenhui [5 ,6 ]
Ze, Yuguan [4 ]
Wang, Ling [7 ]
Zhou, Yingjun [1 ,2 ,3 ]
Hong, Jie [4 ]
Yu, Xiaohong [4 ]
Sheng, Lei [4 ]
Liu, Dong [4 ]
Xu, Bingqing [4 ]
Zhang, Jianhao [5 ]
机构
[1] Huaiyin Normal Univ, Jiangsu Collaborat Innovat Ctr Reg Modern Agr & E, Huaian 223300, Peoples R China
[2] Huaiyin Normal Univ, Jiangsu Key Lab Ecoagr Biotechnol Around Hongze L, Huaian 223300, Peoples R China
[3] Huaiyin Normal Univ, Sch Life Sci, Huaian 223300, Peoples R China
[4] Soochow Univ, Coll Med, Suzhou 215123, Peoples R China
[5] Nanjing Agr Univ, Minist Agr, Key Lab Agr & Anim Prod Proc & Qual Control, Nanjing 210095, Jiangsu, Peoples R China
[6] Suzhou Polytechn Inst Agr, Suzhou 215008, Peoples R China
[7] Lib Soochow Univ, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
Titanium dioxide nanoparticles; Mice; Spermatogenesis; Testis-specific genes; TITANIUM-DIOXIDE NANOPARTICLES; LONG-TERM EXPOSURE; GLYCOGEN-SYNTHASE KINASE-3-BETA; GERM-CELLS; MOLECULAR-MECHANISM; OXIDATIVE DAMAGE; SPLEEN INJURY; DNA-DAMAGE; REPAIR; PROTEIN;
D O I
10.1016/j.jhazmat.2015.08.010
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Although TiO2 nanoparticles (NPs) exposure has been demonstrated to cross blood-testis barrier and accumulate in the testis resulting in the reduction of sperm numbers, limited data with respect to the molecular mechanism of decreased spermatogenesis caused by TiO2 NP exposure. In this research, testicular damage, sperm number and alterations in testis-specific gene expressions in male mice induced by intragastric administration with TiO2 NPs for six months were investigated. It was found out that TiO2 NPs could migrate to cells, deposit in the testis and epididymis and thus cause damages to relevant organs, which are, to be more specific, the reductions of total sperm concentrations and sperm motility and an enhancement in the number of abnormal sperms in the cauda epididymis. Furthermore, the individual expression regarding to the mRNAs and proteins of testis-specific genes, including Cdc2, Cyclin B1, Dmcl, TERT, Tesmin, TESP-1, XPD and XRCCI, were significantly declined, whereas Gsk3-beta and PGAM4 expressions were greatly elevated in mouse testis due to the exposures, which in fact implied that the reduced spermatogenesis may be involved in the alternated testis-specific gene expressions in those exposed male mice. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:718 / 728
页数:11
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