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