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miRNA-211-5p 通过靶向双特异性磷酸酶 6 预测绝经后骨质疏松症的进展并抑制成骨作用。

microRNA-211-5p predicts the progression of postmenopausal osteoporosis and attenuates osteogenesis by targeting dual specific phosphatase 6.

机构信息

Department of Orthopaedics, Second Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.

Department of Orthopaedics, West Hospital of Second Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.

出版信息

Bioengineered. 2022 Mar;13(3):5709-5723. doi: 10.1080/21655979.2021.2017626.

Abstract

Postmenopausal osteoporosis (PMOP) is known as one of the prevalent diseases among middle-aged and elderly women. This paper revolves around the alteration of miR-211-5p in PMOP patients and its function in osteogenic differentiation. Quantitative real-time polymerase chain reaction (qRT-PCR) was implemented to check the miR-211-5p level in the plasma of PMOP patients. Knockdown and overexpression experiments were done to verify the influence of miR-211-5p on human-derived mesenchymal stem cell (hMSC) osteogenic differentiation and osteogenesis. The alkaline phosphatase (ALP) assay kit was taken to test ALP activity. Alizarin red staining monitored osteogenic differentiation, while oil red O staining examined adipogenesis. Western blot confirmed the profiles of osteoclastogenesis-concerned factors (TRAP, NFAT2, c-FOS, Runx2, OCN, CTSK), dual specific phosphatase 6 (DUSP6), ERK, SMAD, and β-catenin. Dual-luciferase reporter and RNA immunoprecipitation assays were implemented to identify the association between miR-211-5p and DUSP6. Our data displayed that miR-211-5p was down-regulated in the PMOP patients' plasma (in contrast with the healthy controls), and it was positively correlated with Vit-D and BMD levels. miR-211-5p overexpression vigorously facilitated hMSC osteogenic differentiation, while miR-211-5p inhibition contributed to the opposite situation. miR-211-5p initiated the ERK/SMAD/β-catenin pathway and repressed DUSP6's expression. Overexpression of DUSP6 counteracted the miR-211-5p-mediated function to a great extent and inactivated ERK/SMAD/β-catenin, whereas enhancing ERK phosphorylation weakened the DUSP6 overexpression-induced function. Consequently, this research unveiled that miR-211-5p promotes osteogenic differentiation by interfering with the DUSP6-mediated ERK/SMAD/β-catenin pathway.

摘要

绝经后骨质疏松症 (PMOP) 是中老年女性中常见的疾病之一。本文围绕 PMOP 患者中 miR-211-5p 的变化及其在成骨分化中的功能展开。采用实时定量聚合酶链反应 (qRT-PCR) 检测 PMOP 患者血浆中的 miR-211-5p 水平。通过敲低和过表达实验验证 miR-211-5p 对人源性间充质干细胞 (hMSC) 成骨分化和成骨的影响。采用碱性磷酸酶 (ALP) 试剂盒检测 ALP 活性。茜素红染色监测成骨分化,油红 O 染色检测脂肪生成。Western blot 证实破骨细胞生成相关因子 (TRAP、NFAT2、c-FOS、Runx2、OCN、CTSK)、双特异性磷酸酶 6 (DUSP6)、ERK、SMAD 和 β-连环蛋白的特征。实施双荧光素酶报告和 RNA 免疫沉淀测定以鉴定 miR-211-5p 与 DUSP6 之间的关联。我们的数据显示,PMOP 患者血浆中的 miR-211-5p 下调(与健康对照组相比),并且与 Vit-D 和 BMD 水平呈正相关。miR-211-5p 过表达有力地促进 hMSC 成骨分化,而 miR-211-5p 抑制则导致相反的情况。miR-211-5p 启动 ERK/SMAD/β-连环蛋白通路并抑制 DUSP6 的表达。DUSP6 的过表达在很大程度上抵消了 miR-211-5p 介导的功能,并使 ERK/SMAD/β-连环蛋白失活,而增强 ERK 磷酸化则削弱了 DUSP6 过表达诱导的功能。因此,这项研究揭示了 miR-211-5p 通过干扰 DUSP6 介导的 ERK/SMAD/β-连环蛋白通路促进成骨分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ec6/8973771/715b7d71bf60/KBIE_A_2017626_F0001_OC.jpg

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