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微小RNA-143与大鼠胚胎着床

MiR-143 and rat embryo implantation.

作者信息

Tian Shi, Su Xing, Qi Lu, Jin Xiao-Hua, Hu Yi, Wang Chun-Ling, Ma Xu, Xia Hong-Fei

机构信息

Haidian Maternal & Child Health Hospital, Beijing 100080, China.

Reproductive and Genetic Center of National Research Institute for Family Planning, Beijing 100081, China; Graduate School, Peking Union Medical College, Beijing 100730, China.

出版信息

Biochim Biophys Acta. 2015 Apr;1850(4):708-21. doi: 10.1016/j.bbagen.2014.11.023. Epub 2014 Dec 5.

Abstract

BACKGROUND

To study the role of miR-143 during embryo implantation in rat.

METHODS

MiR-143 expression in rat early pregnancy was detected by Northern blot. The relation between miR-143 and Lifr predicted and confirmed by bioinformatics method, dual-luciferase activity assay, Western blot and immunohistochemistry. The role of miR-143 was detected by MTS, Edu and ranswell chamber assays.

RESULTS

The expression level of miR-143 on gestation day 5-8 (g.d. 5-8) was higher than on g.d. 3-4 in uteri of pregnant rat. MiR-143 was mainly localized in the superficial stroma/primary decidual zone, luminal and glandular epithelia. The expression of miR-143 was not significantly influenced by pseudopregnancy, but the activation of delayed implantation and experimentally induced decidualization significantly promoted miR-143 expression. Over-expression of miR-143 in human endometrial stromal cells (ESCs) inhibited cell proliferation, migration and invasion. Knockdown of miR-143 promoted cell proliferation and invasion. The results of recombinant luciferase reporters showed that miR-143 could bind to the 3¢-untranslated region (UTR) of leukemia inhibitory factor receptor (Lifr) to inhibit Lifr translation.

CONCLUSIONS

Uterine miR-143 may be involved in the successful pregnancy, especially during the process of blastocyst implantation through regulating Lifr.

GENERAL SIGNIFICANCE

This study may have the potential to provide new insights into the understanding of miR-143 function during embryo implantation.

摘要

背景

研究miR-143在大鼠胚胎植入过程中的作用。

方法

采用Northern印迹法检测大鼠早孕期间miR-143的表达。通过生物信息学方法、双荧光素酶活性测定、蛋白质免疫印迹法和免疫组织化学法预测并证实miR-143与白血病抑制因子受体(Lifr)之间的关系。采用MTS法、Edu法和Transwell小室实验检测miR-143的作用。

结果

妊娠第5 - 8天(g.d. 5 - 8)大鼠子宫中miR-143的表达水平高于妊娠第3 - 4天(g.d. 3 - 4)。miR-143主要定位于浅层基质/初级蜕膜区、腔上皮和腺上皮。假孕对miR-143的表达无显著影响,但延迟着床的激活和实验诱导的蜕膜化显著促进了miR-143的表达。在人子宫内膜基质细胞(ESCs)中过表达miR-143可抑制细胞增殖、迁移和侵袭。敲低miR-143可促进细胞增殖和侵袭。重组荧光素酶报告基因结果显示,miR-143可与白血病抑制因子受体(Lifr)的3′非翻译区(UTR)结合,抑制Lifr的翻译。

结论

子宫miR-143可能参与成功妊娠,尤其是在胚泡植入过程中通过调节Lifr发挥作用。

普遍意义

本研究可能为理解miR-143在胚胎植入过程中的功能提供新的见解。

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