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长链非编码 RNA TUG 通过 miRNA-204/SIRT1 调节骨髓间充质干细胞的成骨分化。

LncRNA TUG regulates osteogenic differentiation of bone marrow mesenchymal stem cells via miRNA-204/SIRT 1.

机构信息

Department of Orthopedic Surgery, Xuzhou Third People's Hospital, Affiliated Xuzhou Hospital of Jiangsu University, China.

出版信息

J Musculoskelet Neuronal Interact. 2022 Sep 1;22(3):401-410.

Abstract

OBJECTIVE

To explore the regulation of LncRNA TUG /miRNA-204/SIRT1 pathway on osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs), so as to provide a new theoretical basis for the clinical treatment of osteoporosis.

METHODS

Detect changes of LncRNA and miRNA expression predicted in post-differentiation BMSCs with Western blot and qPCR tests. Verify the regulatory relationship between LncRNA and miRNA, miRNA and SIRT1 through the luciferase reporter assay. Transfect recombinant plasmids with LncRNA and their shRNA or transfected miRNA mimics and inhibitors.

RESULTS

According to the bioinformatic prediction, LncRNA TUG/miR-204 affected the regulation of SIRT1 on osteogenic differentiation of BMSCs, which were consistent with the results of luciferase reporter assay, namely, there are direct regulation targets between LncRNA TUG and miR-204, miR-204 and SIRT1. Overexpression and knockdown experiments revealed that LncRNA TUG overexpression/knockdown down/up-regulated miR-204 expression, which otherwise increased/decreased SIRT1 levels, and was positively correlated with osteogenic differentiation of BMSCs. Conversely, miR-204 was negatively correlated with LncRNA TUG and SIRT1, and negatively regulated osteogenic differentiation.

CONCLUSION

This study found the direct regulatory relationship of LncRNA TUG/miR-204/SIRT1 during the osteogenic differentiation of BMSCs, and revealed that SIRT1 positively regulates the osteogenic differentiation of BMSCs, which provides a theoretical basis and potential therapeutic targets for a series of osteogenic differentiation-related diseases including osteoporosis.

摘要

目的

探讨长链非编码 RNA(LncRNA)TUG/miRNA-204/SIRT1 通路对骨髓间充质干细胞(BMSCs)成骨分化的调控作用,为骨质疏松症的临床治疗提供新的理论依据。

方法

采用 Western blot 和 qPCR 检测分化后 BMSCs 中预测的 LncRNA 和 miRNA 表达变化。通过荧光素酶报告基因检测验证 LncRNA 和 miRNA、miRNA 和 SIRT1 之间的调控关系。转染 LncRNA 及其 shRNA 或转染 miRNA 模拟物和抑制剂的重组质粒。

结果

根据生物信息学预测,LncRNA TUG/miR-204 影响 SIRT1 对 BMSCs 成骨分化的调节,与荧光素酶报告基因检测结果一致,即 LncRNA TUG 和 miR-204、miR-204 和 SIRT1 之间存在直接调节靶点。过表达和敲低实验表明,LncRNA TUG 过表达/敲低上调/下调 miR-204 表达,反之增加/减少 SIRT1 水平,与 BMSCs 成骨分化呈正相关。相反,miR-204 与 LncRNA TUG 和 SIRT1 呈负相关,负调控成骨分化。

结论

本研究发现了 LncRNA TUG/miR-204/SIRT1 在 BMSCs 成骨分化过程中的直接调节关系,并揭示了 SIRT1 正向调节 BMSCs 的成骨分化,为包括骨质疏松症在内的一系列与成骨分化相关的疾病提供了理论依据和潜在的治疗靶点。

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