LncRNA SNHG14 Delivered by Bone Marrow Mesenchymal Stem Cells-Secreted Exosomes Regulates Osteogenesis and Adipogenesis in Osteoporosis by Mediating the miR-27a-3p/LMNB1 Axis.

IF 3.1 The Kaohsiung journal of medical sciences Pub Date : 2025-05-01 Epub Date: 2025-03-07 DOI:10.1002/kjm2.70004
Jin-Shan Tang, Huai-Xi Yu, Ru-Xin Ruan, Rui Chen, Zi-Qiang Zhu
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Abstract

The purpose of this study was to investigate the role of LncRNA SNHG14 delivered by bone marrow mesenchymal stem cells-secreted exosomes (BMSC-Exos) in osteoporosis (OP). BMSCs and BMSCs-Exos were isolated and identified. BMSCs were transfected, from which BMSCs-Exos were collected. The treated BMSCs-Exos were co-cultured with BMSCs. After osteogenic induction of BMSCs, the calcification was analyzed by alizarin red S staining. After adipogenic induction of BMSCs, lipid droplets were detected by oil red O staining. Glycerol-3-phosphate dehydrogenase activity was measured in BMSCs. OVX mouse models were established and treated with BMSC-EXOs. HE staining and IHC staining were performed on the femurs of mice. The interaction between SNHG14, miR-27a-3p, and LMNB1 was evaluated by luciferase reporter gene assay and RIP assay. Gene levels were assessed using RT-qPCR and Western blot, respectively. BMSC-Exos promoted osteogenic-adipogenic balance of BMSCs. SNHG14 enhanced the promoting effect of BMSCs-Exos on the balance of osteogenesis and adipogenesis of BMSCs. SNHG14 directly bound miR-27a-3p. SNHG1 mediated osteogenic-adipogenic balance in BMSCs via miR-27a-3p. LMNB1 was a target gene of miR-27a-3p. LMNB1 was involved in the process of SNHG14 regulating osteogenic-adipogenic balance in BMSCs. SNHG14 overexpression promoted bone formation and alleviated OP in vivo. SNHG14 delivered by BMSCs-Exos regulates osteogenesis and adipogenesis in OP by mediating the miR-27a-3p/LMNB1 axis.

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骨髓间充质干细胞分泌外泌体传递的LncRNA SNHG14通过介导miR-27a-3p/LMNB1轴调控骨质疏松症的成骨和脂肪发生。
本研究的目的是探讨骨髓间充质干细胞分泌外泌体(BMSC-Exos)传递的LncRNA SNHG14在骨质疏松症(OP)中的作用。分离鉴定BMSCs和BMSCs- exos。转染骨髓间充质干细胞,收集BMSCs- exos。处理后的BMSCs- exos与BMSCs共培养。诱导骨髓间充质干细胞成骨后,茜素红S染色分析其钙化情况。诱导骨髓间充质干细胞成脂后,油红O染色检测脂滴。测定骨髓间充质干细胞中甘油-3-磷酸脱氢酶活性。建立OVX小鼠模型并给予bmscs - exos处理。小鼠股骨进行HE染色和免疫组化染色。通过荧光素酶报告基因实验和RIP实验评估SNHG14、miR-27a-3p和LMNB1之间的相互作用。分别采用RT-qPCR和Western blot检测基因水平。BMSCs - exos促进BMSCs成骨-脂肪平衡。SNHG14增强了BMSCs- exos对BMSCs成骨和脂肪生成平衡的促进作用。SNHG14直接结合miR-27a-3p。SNHG1通过miR-27a-3p介导BMSCs成骨-脂肪平衡。LMNB1是miR-27a-3p的靶基因。LMNB1参与了SNHG14调节BMSCs成骨-脂肪平衡的过程。SNHG14过表达促进骨形成,减轻OP。由BMSCs-Exos传递的SNHG14通过介导miR-27a-3p/LMNB1轴调控OP的成骨和脂肪生成。
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