Impact of preimplantational oral low-dose estradiol-17 exposure on the endometrium: The role of miRNA

被引:9
|
作者
Floeter, Veronika L. [1 ,2 ]
Lorenz, Anne-Kathrin [1 ,2 ]
Kirchner, Benedikt [2 ]
Pfaffl, Michael W. [2 ]
Bauersachs, Stefan [1 ]
Ulbrich, Susanne E. [1 ]
机构
[1] Swiss Fed Inst Technol, Anim Physiol, Inst Agr Sci, Univ Str 2, CH-8092 Zurich, Switzerland
[2] Tech Univ Munich, Sch Life Sci, Dept Anim Physiol & Immunol, Life Sci Ctr Weihenstephan, Freising Weihenstephan, Germany
基金
瑞士国家科学基金会;
关键词
deep sequencing; endocrine disrupting chemicals; estrogen; pig; pregnancy; BREAST-CANCER CELLS; ENDOCRINE-DISRUPTING CHEMICALS; ESTROGEN-RECEPTOR-ALPHA; GENE-EXPRESSION; MICRORNA EXPRESSION; REPRODUCTIVE-SYSTEM; PREGNANCY; METHOXYCHLOR; MAINTENANCE; BIOGENESIS;
D O I
10.1002/mrd.22975
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
Porcine conceptuses synthesize estrogens between Day 11 and 12 as signal for maternal recognition of pregnancy. A preimplantational estrogen exposure to pregnant gilts has been associated with embryonic losses and changes in endometrial mRNA expression. MicroRNAs (miRNAs) play a key role in the mRNA regulation by modulating the expression. Effects of estrogens on endometrial miRNAs have not been investigated in this context so far. Thus, we studied the endometrial expression profile of miRNAs in the pig at gestational Day 10 after daily estradiol-17 (E2) application starting at fertilization using either 0, 0.05 (ADIacceptable daily intake), 10 (NOELno-observed-effect level) and 1,000 (high dose) mu g E2/kg body weight/day, respectively. In endometrial homogenates, E2 (p < 0.001) and total estrogen concentrations (p < 0.001) were significantly increased, namely 28- and 160-fold, respectively, in the high dose group as compared to the control. Additionally, total estrogens were sixfold elevated in the NOEL group. Interestingly, high-throughput sequencing of small non-coding RNA libraries did not indicate any differentially expressed miRNAs between the treatment groups and the control group. The expression of 12 potential E2 target miRNAs investigated by RT-qPCR were equally unaffected. Thus, preimplantational E2 exposure resulted in significantly higher endometrial estrogen concentrations, but did not perturb the expression profile of endometrial miRNAs.
引用
收藏
页码:417 / 426
页数:10
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