Biphasic effects of perfluorooctanoic acid on steroidogenesis in mouse Leydig tumour cells

被引:20
作者
Tian, Meiping [1 ,2 ]
Huang, Qingyu [1 ]
Wang, Heng [3 ]
Martin, Francis L. [4 ]
Liu, Liangpo [1 ]
Zhang, Jie [1 ]
Shen, Heqing [1 ]
机构
[1] Chinese Acad Sci, Inst Urban Environm, Key Lab Urban Environm & Hlth, Xiamen 361021, Fujian, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Zhoushan Municipal Ctr Dis Control & Prevent, Key Lab Hlth Risk Factors Seafood Zhejiang Prov, Zhoushan 316021, Zhejiang, Peoples R China
[4] Univ Cent Lancashire, Sch Pharm & Biomed Sci, Preston PR1 2HE, Lancs, England
关键词
Perfluorooctanoic acid; Endocrine disruption; Biphasic effects; MLTC-1; cells; Steroidogenesis; Steroid hormone; HUMAN SEMEN QUALITY; PERFLUOROALKYL ACIDS; GENE-EXPRESSION; REPRODUCTIVE HORMONES; SULFONATE PFOS; EXPOSURE; SERUM; ASSOCIATIONS; ELIMINATION; DISTURBANCE;
D O I
10.1016/j.reprotox.2018.11.006
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Perfluorooctanoic acid (PFOA) is a persistent organic pollutant, which may possess endocrine disrupting properties. Herein, we investigated the possible mechanism(s) of toxicity and steroidogenesis in mouse Leydig cells. MLTC-1 (mouse Leydig tumour cells) cells were exposed to 0, 50, 100 or 200 mu M PFOA for 48 h to ascertain their effects on the nuclear (membrane) receptor responses, steroidogenesis pathway and related regulated gene expression and steroid hormone secretion profiles. Our results reveal that nuclear receptors PXR, SR-B1 and LHR are sensitive to PFOA exposure. PFOA can accumulate in mitochondria and alter cholesterol precursor (fatty acid) mitochondrial transport process-related gene expression and thus inhibit steroid hormone precursor (cholesterol) production. In particular, PFOA exhibits biphasic effects on testosterone and progesterone production at differing levels of exposure. These findings indicate the potential endocrine-related effects of PFOA on steroid hormone secretion in Leydig cells and point to a novel disruption model.
引用
收藏
页码:54 / 62
页数:9
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