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首页> 外文期刊>Theriogenology >miRNA-185 regulates retained fetal membranes of cattle by targeting STIM1
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miRNA-185 regulates retained fetal membranes of cattle by targeting STIM1

机译:miRNA-185通过靶向溶液调节牛的保留胎膜

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摘要

Retained fetal membranes (RFM) of cows is an important reproductive disturbance, and is related to miRNA-185. Stromal interaction molecule 1 (STIM1), a potential target gene of miRNA-185, could influence placenta release via regulating Ca2+ concentration intracellular. The aim of this study was to explore the mechanism of RFM by investigating the regulatory relationship between miRNA-185 and STIM1 in primary uterine caruncel epithelial (UCE) cells. Serum samples of healthy Holstein dairy cows (n = 20) and RFM cows (n = 12), with a similar age, parity, weight, and milk yield, were collected to detect Ca2+ concentration at prepartum 1-5 d and postpartum 6, 12 and 24 h. Caruncle tissues were collected from healthy (n = 6) and RFM cows (n = 6) at 12 h after calving. Quantitative polymerase chain reaction (Q-PCR) and western blotting (WB) were performed to detect the mRNA and protein levels of STIM1, respectively. UCE cells were cultured by the explant culture method, further purified, and subsequently treated with PmirGLO-STIM1-Mut + miRNA-185 mimics and mirGLO-STIM1-Mut + miRNA-185 NC. Q-PCR and WB were performed to detect mRNA and protein levels of STIM1 with treated miRNA-185 mimics. Serum levels of Ca2+ from RFM cows were abnormally decreased at prepartum 1 d and postpartum 6, 12 and 24 h. Expression level of STIM1 was down-regulated in the caruncle tissue of RFM cows. The luciferase activity was decresed about 30.9% by miRNA-185 mimics (p & 0.01), and the mRNA and protein levels of STIM1 were downregulated miRNA-185-mimics. It was suggesting that miRNA-185 might play an important role in RFM through regulating the expression of STIM1. (C) 2018 Elsevier Inc. All rights reserved.
机译:保留胎膜(RFM)的奶牛是重要的生殖紊乱,与miRNA-185有关。基质相互作用分子1(STIM1),miRNA-185的潜在靶基因,可以通过调节Ca 2 +浓度细胞内通过调节胎盘释放。本研究的目的是通过研究MiRNA-185和初级子宫肌肉上皮(UCE)细胞的调节关系来探讨RFM的机制。收集具有相似年龄,奇偶校验,重量和牛奶产量的健康荷斯坦奶牛(n = 20)和RFM奶牛(n = 12)的血清样本,以检测预备1-5 d和产后6的Ca2 +浓度, 12和24小时。在产犊后12小时从健康(n = 6)和RFM奶牛(n = 6)收集CARUNCLE组织。进行定量聚合酶链式反应(Q-PCR)和蛋白质印迹(WB)以分别检测STIM1的mRNA和蛋白质水平。通过脱钙培养方法培养UCE细胞,进一步纯化,随后用PMILGLO-STIM1-MUT + miRNA-185模拟物和MIRGLO-STIM1-MUT + miRNA-185nc处理。进行Q-PCR和Wb以检测MRNA和蛋白质水平的溶性与处理的miRNA-185模拟物。从RFM奶牛的血清CA2 +的CA2 +在Prepartum 1 D和产后6,12和24小时异常降低。在RFM奶牛的Caruncle组织中,Stim1的表达水平下调。通过MiRNA-185模拟物(P& 0.01),荧光素酶活性约为30.9%。这表明MiRNA-185可以通过调节Stim1的表达,在RFM中发挥重要作用。 (c)2018年Elsevier Inc.保留所有权利。

著录项

  • 来源
    《Theriogenology》 |2019年第2019期|共6页
  • 作者单位

    Heilongjiang Bayi Agr Univ Coll Anim Sci &

    Vet Med Daqing 163319 Peoples R China;

    Heilongjiang Bayi Agr Univ Coll Anim Sci &

    Vet Med Daqing 163319 Peoples R China;

    Heilongjiang Bayi Agr Univ Coll Anim Sci &

    Vet Med Daqing 163319 Peoples R China;

    Heilongjiang Bayi Agr Univ Coll Anim Sci &

    Vet Med Daqing 163319 Peoples R China;

    Heilongjiang Bayi Agr Univ Coll Anim Sci &

    Vet Med Daqing 163319 Peoples R China;

    Heilongjiang Bayi Agr Univ Coll Anim Sci &

    Vet Med Daqing 163319 Peoples R China;

    Heilongjiang Bayi Agr Univ Coll Anim Sci &

    Vet Med Daqing 163319 Peoples R China;

    Heilongjiang Bayi Agr Univ Coll Anim Sci &

    Vet Med Daqing 163319 Peoples R China;

    Heilongjiang Bayi Agr Univ Coll Anim Sci &

    Vet Med Daqing 163319 Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 动物学;
  • 关键词

    Retained fetal membranes; miRNA-185; STIM1; Ca2+;

    机译:保留胎膜;miRNA-185;STIM1;CA2 +;

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