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肿瘤坏死因子-α通过下调微小RNA-34a的表达抑制骨髓干细胞向成骨细胞分化。

Tumor Necrosis Factor-α Inhibits Bone Marrow Stem Cell Differentiation into Osteoblasts by Downregulating microRNA-34a Expression.

作者信息

Xin Wei, Wang Xuxia, Zhang Wenjuan, Zhu Haiyan, Dong Rui, Zhang Jun

机构信息

Shandong Provincial Key Laboratory of Oral Tissue Regeneration, School of Stomatology, Shandong University, Jinan, Shandong Province, China.

Department of Orthodontics, Faculty of Stomatology, Shandong University, Jinan, China.

出版信息

Ann Clin Lab Sci. 2019 May;49(3):324-329.

Abstract

OBJECTIVE

In this study, we aimed to investigate the role of microRNAs in modulating osteogenesis in the inflammatory milieu.

METHODS

Bone marrow stem cells were isolated from C57/BL mice. Tumor necrosis factor-alpha (TNF-α) (0-10 ng/ml) was added to the cell medium to mimic an inflammatory reaction. Cell apoptosis and proliferation were evaluated by flow cytometry and CyQUANT direct cell proliferation assay respectively. MicroRNA expression was measured by real-time PCR. Then miR-34a precursors were transfected into BMSCs to evaluate the influence of miR-34a on TNF-α induced suppression.

RESULTS

Our results indicated that TNF-α significantly inhibited BMSC proliferation and differentiation in a dose-dependent manner. In addition, TNF-α significantly decreased mRNA expression level of osteocalcin (OC) and alkaline phosphatase (ALP). TNF-α treatment decreased miR-34a levels, and miR-34a precursors reversed the impact of TNF-α on BMSC proliferation and differentiation.

CONCLUSIONS

Importantly, miR-34a promotes osteogenic differentiation and reverses proinflammatory cytokine influence, indicating that a miR-34a-targeted therapy could be a promising approach to promote bone regeneration.

摘要

目的

在本研究中,我们旨在探究微小RNA在炎症环境中对骨生成调节作用。

方法

从C57/BL小鼠中分离骨髓干细胞。将肿瘤坏死因子-α(TNF-α)(0 - 10纳克/毫升)添加到细胞培养基中以模拟炎症反应。分别通过流式细胞术和CyQUANT直接细胞增殖测定法评估细胞凋亡和增殖。通过实时聚合酶链反应测量微小RNA表达。然后将miR-34a前体转染到骨髓间充质干细胞中,以评估miR-34a对TNF-α诱导的抑制作用的影响。

结果

我们的结果表明,TNF-α以剂量依赖性方式显著抑制骨髓间充质干细胞增殖和分化。此外,TNF-α显著降低骨钙素(OC)和碱性磷酸酶(ALP)的信使核糖核酸表达水平。TNF-α处理降低了miR-34a水平,并且miR-34a前体逆转了TNF-α对骨髓间充质干细胞增殖和分化的影响。

结论

重要的是,miR-34a促进成骨分化并逆转促炎细胞因子的影响,表明以miR-34a为靶点的治疗可能是促进骨再生的一种有前景的方法。

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