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LncRNA MSC-AS1 promotes osteogenic differentiation and alleviates osteoporosis through sponging microRNA-140-5p to upregulate BMP2

机译:LNCRNA MSC-AS1促进成骨分化,并通过海绵微小-140-5P来缓解骨质疏松症,以上调BMP2

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摘要

This study aims to explore the role of lncRNA MSC-AS1/microRNA-140-5p/BMP2 regulatory loop in promoting osteogenic differentiation of BMSCs. BMSCs were isolated from bone marrow of mice. Expression levels of MSC-AS1, microRNA-140-5p and BMP2 during osteogenic differentiation were detected by qRT-PCR. Meanwhile, regulatory effect of MSC-AS1 on osteogenic differentiation was detected through ALP staining and alizarin red staining. The binding sites between microRNA-140-5p and MSC-AS1 as well as between microRNA-140-5p and BMP2 were predicted by TargetScan, which were further confirmed by dual-luciferase reporter gene assay. In addition, protein levels of MSC-AS1/ microRNA-140-5p/BMP2 were detected by Western blot. Finally, rescue experiments were conducted to clarify the regulatory effects of MSC-AS1/microRNA-140-5p/BMP2 axis on osteogenic differentiation. MSC-AS1 and BMP2 were found to be remarkably up-regulated during osteogenic differentiation, while microRNA-140-5p was conversely down-regulated. Meanwhile, knockdown of MSC-AS down-regulated expression levels of osteogenesis-associated genes and weakened the mineralization capacity of BMSCs. MicroRNA-140-5p was verified to bind to the 3'UTR of MSC-AS1 and BMP2 genes. Knockdown of MSC-AS1 in BMSCs could reduce the expression of microRNA-140-5p, while knockdown of microRNA-140 -5p also down-regulated BMP2 level. In addition, co-silence of MSC-AS1 and microRNA-140-5p reversed the inhibitory effect of MSC-AS1 knockdown on osteogenic differentiation and protein levels of p-Smad1/5/8, RUNX2 and Osterix. MSC-AS1 might promote the osteogenic differentiation of BMSCs through sponging microRNA-140-5p to up-regulate BMP2, thus alleviating the progression of osteoporosis. (C) 2019 Elsevier Inc. All rights reserved.
机译:本研究旨在探讨LNCRNA MSC-AS1 / microRNA-140-5P / BMP2调节因子在促进BMSCs的骨质发生分化方面的作用。 BMSCs与小鼠的骨髓中分离出来。通过QRT-PCR检测骨质发生分化期间MSC-AS1,MicroRNA-140-5P和BMP2的表达水平。同时,通过Alp染色和茜素红染色来检测MSC-AS1对骨质发生分化的调节作用。通过TargetScan预测MicroRNA-140-5P和MSC-AS1和MICRNA-140-5P和BMP2之间的结合位点,其通过双荧光素酶报告基因测定进一步证实。此外,通过Western印迹检测MSC-AS1 / microRNA-140-5P / BMP2的蛋白质水平。最后,进行了救援实验,以阐明MSC-AS1 / microRNA-140-5P / BMP2轴对成骨分化的调节作用。发现MSC-AS1和BMP2在成骨分化期间显着上调,而MicroRNA-140-5P相反调节。同时,MSC - 作为骨质发生相关基因的下调表达水平,削弱了BMSC的矿化能力。验证MicroRNA-140-5P以结合MSC-AS1和BMP2基因的3'UTR。 BMSC中MSC-AS1的敲低可以减少MicroRNA-140-5P的表达,而MicroRNA-140 -5P的敲低也会下调BMP2水平。此外,MSC-AS1和MicroRNA-140-5P的共静脉反转MSC-AS1敲低对P-Smad1 / 5/8,Runx2和Osterix的骨质发生分化和蛋白质水平的抑制作用。 MSC-AS1可以通过海绵微润罗纳-140-5P来促进BMSC的成骨分化为上调BMP2,从而减轻骨质疏松症的进展。 (c)2019 Elsevier Inc.保留所有权利。

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    First Peoples Hosp Changzhou Dept Traumat Orthoped 183 Jvqian St Changzhou 213003 Jiangsu;

    First Peoples Hosp Changzhou Dept Traumat Orthoped 183 Jvqian St Changzhou 213003 Jiangsu;

    First Peoples Hosp Changzhou Dept Traumat Orthoped 183 Jvqian St Changzhou 213003 Jiangsu;

    First Peoples Hosp Changzhou Dept Traumat Orthoped 183 Jvqian St Changzhou 213003 Jiangsu;

    First Peoples Hosp Changzhou Dept Traumat Orthoped 183 Jvqian St Changzhou 213003 Jiangsu;

    First Peoples Hosp Changzhou Dept Traumat Orthoped 183 Jvqian St Changzhou 213003 Jiangsu;

    First Peoples Hosp Changzhou Dept Traumat Orthoped 183 Jvqian St Changzhou 213003 Jiangsu;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

    osteoporosis; MSC-AS1; MicroRNA-140-5p; BMP2;

    机译:骨质疏松症;MSC-AS1;microRNA-140-5P;BMP2;

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