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首页> 外文期刊>Bone >Long non-coding RNA H19 mediates mechanical tension-induced osteogenesis of bone marrow mesenchymal stem cells via FAK by sponging miR-138
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Long non-coding RNA H19 mediates mechanical tension-induced osteogenesis of bone marrow mesenchymal stem cells via FAK by sponging miR-138

机译:长期非编码RNA H19通过冲把MIR-138通过FAK介导机械张力诱导的骨髓间充质干细胞的骨质发生。

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摘要

Abstract Bone marrow mesenchymal stem cells (BMMSCs) provide the biological basis for bone reconstruction. Mechanical tension stimulation as a potent modulator is able to promote osteogenic capability of BMMSCs. Long non-coding RNAs (LncRNAs) as competing endogenous RNAs (ceRNAs) for microRNAs, are postulated to regulate the osteogenic differentiation of stem cells. However, the mechanism how (whether) lncRNAs mediates tension-induced osteogenesis of BMSCs still remains poor understood. Here, human BMMSCs (hBMMSCs) were subjected to mechanical tension (10%, 0.5Hz). Results showed that mechanical tension could enhance osteogenic differentiation and increase H19 expression. H19 deficiency suppressed tension-induced osteogenic differentiation, demonstrating that H19 could mediate tension-induced osteogenesis in hBMMSCs. Besides, mechanical tension could suppress miR-138 expression, and down-regulated miR-138 promoted tension-induced osteogenesis in hBMMSCs. Luciferase reporter assays illustrated that H19 had binding sites with miR-138, and H19 deficiency increased miR-138 level, demonstrating that H19 may act as a ceRNA for miR-138 in hBMMSCs. Luciferase reporter assays also showed that miR-138 could target PTK2,a gene encoding focal adhesion kinase (FAK). Up-regulated miR-138 impaired increased FAK expression induced by mechanical tension. The relationship among H19, miR-138 and FAK under tension condition was further studied. H19 deficiency inhibited FAK expression, which could be partly rescued by knock-downing miR-138. In addition, suppressed tension-induced osteogenic differentiation in H19 defective cells was partly rescued by miR-138 knockdown. Taken together, this study indicated that H19 is a positive regulator in tension-induced osteogenesis of hBMMSCs through acting as a ceRNA for miR-138 and then up-regulating downstream FAK. Highlights ? Mechanical tension could enhance osteogenesis of hBMMSCs. ? Long non-coding RNA H19 mediates mechanical tension-induced osteogenesis. ? H19 acts as a sponge to hijack miR-138 under tension strain. ? H19 as ceRNA for miR-138 regulates tension-induced osteogenesis via downstream FAK.
机译:摘要骨髓间充质干细胞(BMMSCs)为骨重建提供生物学依据。作为有效调节剂的机械张力刺激能够促进BMMSCs的成骨能力。长期非编码RNA(LNCRNA)作为MicroRNA的竞争内源RNA(CERNAS),假设用于调节干细胞的成骨分化。然而,如何(无论是否)介导张力诱导的BMSC的骨质发生仍然仍然较差。这里,人体BMMSCs(HBMMSCs)受到机械张力(10%,0.5Hz)。结果表明,机械张力可提高成骨分化和增加H19表达。 H19缺乏抑制张力诱导的成骨分化,表明H19可以在HBMMSCs中介导张力诱导的骨质发生。此外,机械张力可以抑制miR-138表达,下调的miR-138在HBMMSC中促进张力诱导的骨质发生。荧光素酶报告者分析说明H19具有MiR-138的结合位点,H19缺乏增加miR-138水平,表明H19可以作为MiR-138的Cerna在HBMMSCS中充当Cerna。荧光素酶报告器分析还显示MIR-138可以靶向PTK2,该基因编码局灶性粘附激酶(FAK)。上调的miR-138受到机械张力诱导的增加的FAK表达增加。进一步研究了H19,MIR-138和FAK之间的关系。 H19缺乏症抑制了FAK表达,可以通过击倒miR-138部分救出。此外,抑制H19缺陷细胞中的张力诱导的骨质发生分化部分通过miR-138敲低来抵押。在一起,本研究表明,H19是张力诱导的HBMMSCS的阳性调节剂,通过作为MIR-138的CERNA,然后用作下游FAK的CERNA。强调 ?机械张力可以增强HBMMSCS的骨质发生。还长期非编码RNA H19介导机械张力诱导的成骨发生。还H19在张力应变下充当劫持miR-138的海绵。还作为miR-138的Cerna作为MiR-138的Cerna通过下游FAK调节紧张诱导的成骨。

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