刘薇

个人信息Personal Information

教授

博士生导师

硕士生导师

主要任职:环境学院副院长

其他任职:环境学院教工党支部副书记

性别:女

毕业院校:大连理工大学

学位:博士

所在单位:环境学院

联系方式:Email:Liu_wei@dlut.edu.cn

电子邮箱:liu_wei@dlut.edu.cn

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DEHP exposure in utero disturbs sex determination and is potentially linked with precocious puberty in female mice

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论文类型:期刊论文

发表时间:2016-09-15

发表刊物:TOXICOLOGY AND APPLIED PHARMACOLOGY

收录刊物:SCIE、PubMed、Scopus

卷号:307

页面范围:123-129

ISSN号:0041-008X

关键字:DEHP; In utero exposure; Sex determination; Follicular atresia; Gonadal development; Granulosa cells

摘要:Human's ubiquitous exposure to di (2-ethylhexyl) phthalate (DEHP) is thought to be associated with female reproductive toxicity. Previous studies found that DEHP inhibited follicle growth and decreased estradiol levels in adult female mice. However, limited information is available on the link between in utero DEHP exposure and ovarian development in female mouse offspring. The present study evaluates the disturbances in regulatory genes involved in female sex determination and the ovarian outcomes in fetal and postnatal female mice treated with in utero DEHP exposure. Pregnant mice were exposed to DEHP by gavage, with the dosage regime beginning at human relevant exposure levels. After in utero DEHP exposure, increased follicular atresia was observed in the female pups at postnatal days (PND) 21. Foxl2 expression was significantly upregulated, and Fst was significantly downregulated by DEHP above 2 mg/kg/d at PND 1 and 21. This suggests that lesion of granulosa cell differentiation and disturbance of follicle development in postnatal female mice. The expression of Cyp11a1 and Star were significantly downregulated by in utero DEHP exposure, indicating effects on estradiol biosynthesis. The female sex determination pathway was disturbed in fetus by DEHP at 2 mg/kg/d and above during the critical time window of sex determination causing significant upregulation of Foxl2, Wnt4, beta-catenin and Fst. Furthermore, the increased expression of Wnt4 was supported by whole-mount in situ hybridization (WISH). These results suggest a possible association between in utero DEHP exposure and precocious puberty in the postnatal life of mice offspring, where disturbance of the sex determination regulating pathway acted as an important mechanism. (C) 2016 Elsevier Inc. All rights reserved.