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miR-133a-3p inhibits the osteogenic differentiation of bone marrow mesenchymal stem cells by regulating ankyrin repeat domain 44

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机构: [1]Capital Med Univ, Beijing Tongren Hosp, Dept Orthoped, Beijing, Peoples R China [2]Capital Med Univ, Beijing Stomatol Hosp & Sch Stomatol, Beijing Key Lab, Beijing Inst Dent Res, Beijing, Peoples R China [3]Wenxi People Hosp Shanxi Prov, Dept Neurosurg, Wenxi, Peoples R China [4]Shanghai Yapeng Biotechnol Co LTD, Shanghai Yapeng Biol Technol Co LTD, Res & Invent Ctr, Shanghai, Peoples R China [5]Dalian Med Univ, Affiliated Hosp 1, Dept Orthoped, 5 Longbin Rd, Dalian, Liaoning, Peoples R China
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关键词: miR-133a-3p Osteogenic differentiation BMSCs ANKRD44

摘要:
In this study, we aimed to identify the specific microRNAs (miRNAs) that are involved in the osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) from ovariectomized (OVX) mice, and to further explore the mechanism by which these miRNAs regulate osteogenic differentiation. Based on the existing studies, the expression of seven miRNAs in BMSCs from OVX mice was evaluated using quantitative reverse transcription polymerase chain reaction (qRT-PCR). The expression of miR-133a-3p and osteogenesis-related genes (runt-related transcription factor 2 (Runx2), Osterix, alkaline phosphatase (ALP), and osteopontin) in BMSCs treated with miR-133a-3p mimics or inhibitors was detected by qRT-PCR or Western blotting. Osteogenesis efficiency was determined using ALP and alizarin red staining. The effector-target relationship between miR-133a-3p and ankyrin repeat domain 44 (ANKRD44) was confirmed by bioinformatics and a dual luciferase assay. Among the seven selected miRNAs, miR-133a-3p expression was significantly increased in BMSCs from OVX mice. Overexpression of miR-133a-3p dramatically inhibited the expression of osteogenesis-related genes in BMSCs and reduced ALP activity and mineralization. However, these processes were markedly ameliorated upon miR-133a-3p inhibition. Moreover, miR-133a-3p appeared to target ANKRD44, and the ANKRD44 expression was negatively regulated by miR-133a3p. Furthermore, ANKRD44 upregulation eliminated the anti-osteogenic differentiation effects of miR-133a-3p in BMSCs. Thus, our results indicated that miR-133a-3p inhibits the osteogenic differentiation of BMSCs by suppressing ANKRD44.

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出版当年[2020]版:
大类 | 4 区 生物
小类 | 4 区 生化与分子生物学 4 区 生物物理 4 区 生理学
最新[2023]版:
大类 | 4 区 生物学
小类 | 4 区 生化与分子生物学 4 区 生物物理 4 区 生理学
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出版当年[2019]版:
Q4 BIOPHYSICS Q4 PHYSIOLOGY Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
最新[2023]版:
Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Q4 BIOPHYSICS Q4 PHYSIOLOGY

影响因子: 最新[2023版] 最新五年平均 出版当年[2019版] 出版当年五年平均 出版前一年[2018版] 出版后一年[2020版]

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第一作者机构: [1]Capital Med Univ, Beijing Tongren Hosp, Dept Orthoped, Beijing, Peoples R China
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通讯机构: [5]Dalian Med Univ, Affiliated Hosp 1, Dept Orthoped, 5 Longbin Rd, Dalian, Liaoning, Peoples R China [*1]Department of Orthopedics, The First Affiliated Hospital of Dalian Medical University, No. 5, Longbin Road, Dalian Development Zone, Dalian, Liaoning Province, China
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