microRNA-324-3p通过抑制SMAD7促进成骨细胞分化

IF 0.3 4区 医学 Q4 ENGINEERING, BIOMEDICAL Journal of Hard Tissue Biology Pub Date : 2022-01-01 DOI:10.2485/jhtb.31.263
Wei Xu, Rui Xia, Feng Tian, Lei Liu, Mengmeng Li, Shi-yuan Fang
{"title":"microRNA-324-3p通过抑制SMAD7促进成骨细胞分化","authors":"Wei Xu, Rui Xia, Feng Tian, Lei Liu, Mengmeng Li, Shi-yuan Fang","doi":"10.2485/jhtb.31.263","DOIUrl":null,"url":null,"abstract":": Fracture healing is a complex dynamic process that involves the balance between osteoblasts and osteoclasts. Sev-eral microRNAs (miRNAs) have been shown to participate in fracture healing. In this study, we investigated the role of miR-324-3p in osteoblast differentiation. MC3T3-E1 cell differentiation was induced by icariin, and miR-324-3p expression levels during cell differentiation were measured using qRT-PCR. Cell proliferation and differentiation were assessed to eval uate the function of miR-324-3p. Luciferase activity was used for target gene verification. During MC3T3-E1 differentia tion, miR-324-3p levels gradually increased over time. Further experiments showed that miR-324-3p overexpression significantly promoted cell viability, whereas miR-324-3p downregulation showed the opposite effect. For cells with miR-324-3p mimic, the levels of bone sialoprotein, Runx2, osteocalcin, and alkaline phosphatase activity were significantly elevated. SMAD7 is the target gene of miR-324-3p, and its level is gradually downregulated during MC3T3-E1 cell differentiation. MiR-324-3p may promote MC3T3-E1 cell differentiation by targeting SMAD7.","PeriodicalId":16040,"journal":{"name":"Journal of Hard Tissue Biology","volume":"1 1","pages":""},"PeriodicalIF":0.3000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"microRNA-324-3p Promotes Osteoblasts Differentiation via Suppressing SMAD7\",\"authors\":\"Wei Xu, Rui Xia, Feng Tian, Lei Liu, Mengmeng Li, Shi-yuan Fang\",\"doi\":\"10.2485/jhtb.31.263\",\"DOIUrl\":null,\"url\":null,\"abstract\":\": Fracture healing is a complex dynamic process that involves the balance between osteoblasts and osteoclasts. Sev-eral microRNAs (miRNAs) have been shown to participate in fracture healing. In this study, we investigated the role of miR-324-3p in osteoblast differentiation. MC3T3-E1 cell differentiation was induced by icariin, and miR-324-3p expression levels during cell differentiation were measured using qRT-PCR. Cell proliferation and differentiation were assessed to eval uate the function of miR-324-3p. Luciferase activity was used for target gene verification. During MC3T3-E1 differentia tion, miR-324-3p levels gradually increased over time. Further experiments showed that miR-324-3p overexpression significantly promoted cell viability, whereas miR-324-3p downregulation showed the opposite effect. For cells with miR-324-3p mimic, the levels of bone sialoprotein, Runx2, osteocalcin, and alkaline phosphatase activity were significantly elevated. SMAD7 is the target gene of miR-324-3p, and its level is gradually downregulated during MC3T3-E1 cell differentiation. MiR-324-3p may promote MC3T3-E1 cell differentiation by targeting SMAD7.\",\"PeriodicalId\":16040,\"journal\":{\"name\":\"Journal of Hard Tissue Biology\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.3000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Hard Tissue Biology\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.2485/jhtb.31.263\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"ENGINEERING, BIOMEDICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Hard Tissue Biology","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.2485/jhtb.31.263","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
引用次数: 1

摘要

骨折愈合是一个复杂的动态过程,涉及到成骨细胞和破骨细胞之间的平衡。一些microRNAs (miRNAs)已被证明参与骨折愈合。在这项研究中,我们研究了miR-324-3p在成骨细胞分化中的作用。淫羊藿苷诱导MC3T3-E1细胞分化,采用qRT-PCR检测细胞分化过程中miR-324-3p的表达水平。通过评估细胞增殖和分化来评估miR-324-3p的功能。荧光素酶活性用于靶基因验证。在MC3T3-E1分化过程中,miR-324-3p水平随时间逐渐升高。进一步的实验表明,miR-324-3p过表达可显著提高细胞活力,而miR-324-3p下调则相反。对于含有miR-324-3p模拟物的细胞,骨唾液蛋白、Runx2、骨钙素水平和碱性磷酸酶活性显著升高。SMAD7是miR-324-3p的靶基因,其水平在MC3T3-E1细胞分化过程中逐渐下调。MiR-324-3p可能通过靶向SMAD7促进MC3T3-E1细胞分化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
microRNA-324-3p Promotes Osteoblasts Differentiation via Suppressing SMAD7
: Fracture healing is a complex dynamic process that involves the balance between osteoblasts and osteoclasts. Sev-eral microRNAs (miRNAs) have been shown to participate in fracture healing. In this study, we investigated the role of miR-324-3p in osteoblast differentiation. MC3T3-E1 cell differentiation was induced by icariin, and miR-324-3p expression levels during cell differentiation were measured using qRT-PCR. Cell proliferation and differentiation were assessed to eval uate the function of miR-324-3p. Luciferase activity was used for target gene verification. During MC3T3-E1 differentia tion, miR-324-3p levels gradually increased over time. Further experiments showed that miR-324-3p overexpression significantly promoted cell viability, whereas miR-324-3p downregulation showed the opposite effect. For cells with miR-324-3p mimic, the levels of bone sialoprotein, Runx2, osteocalcin, and alkaline phosphatase activity were significantly elevated. SMAD7 is the target gene of miR-324-3p, and its level is gradually downregulated during MC3T3-E1 cell differentiation. MiR-324-3p may promote MC3T3-E1 cell differentiation by targeting SMAD7.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Hard Tissue Biology
Journal of Hard Tissue Biology ENGINEERING, BIOMEDICAL-
CiteScore
0.90
自引率
0.00%
发文量
28
审稿时长
6-12 weeks
期刊介绍: Information not localized
期刊最新文献
Evaluation of Maxillary First Molar Intrusion Mechanics with Mini-Implant Anchorages Using the Finite Element Method Study on the Effect of Soft-Start Light on Microleakage in Pit and Fissure Closure Upregulation of miR-101-3p Overcomes Ibrutinib Resistance by Targeting ABCC5 in Diffuse Large B-Cell Lymphoma (DLBCL) miR-141 Improve Osteoporosis by Promoting Osteoblast Differentiation through Targeting RICTOR A Study of Submandibular Gland Changes in Mice of a Murine Model of Sjögren’s Syndrome Administered Dental Pulp Stem Cell-Conditioned Medium
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1