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miR-203 对于绝经后骨质疏松症骨髓间充质干细胞从成骨分化向成脂分化的转变是必需的。

MiR-203 is essential for the shift from osteogenic differentiation to adipogenic differentiation of mesenchymal stem cells in postmenopausal osteoporosis.

机构信息

Department of Arthropodidae, Shanghai Guanghua Hospitals of Traditional Chinese and Western Medicine, Shanghai, China.

出版信息

Eur Rev Med Pharmacol Sci. 2018 Sep;22(18):5804-5814. doi: 10.26355/eurrev_201809_15906.

Abstract

OBJECTIVE

The purpose of this study was to investigate how miR-203 promotes osteogenic differentiation of bone marrow mesenchymal cells (BMSCs) by regulating its target gene DKK1, thereby inhibiting the occurrence of osteoporosis.

PATIENTS AND METHODS

A total of 60 cases with postmenopausal osteoporosis and 40 cases of normal individuals were recruited. The expression of miR-203 in serum of all cases was detected by quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR). The capacity of osteogenesis and adipogenic differentiation of MSCs was determined by alizarin red staining and oil red staining, respectively. Transfection of miR-203 mimics and miR-203 inhibitor were mediated by Liposomes, and then the MSCs were induced osteogenic and adipogenic differentiation. MiR-203 mimic was co-transfected with wild-type or mutant DKK1 for luciferase reporter gene detection. In the osteoporosis model of rats, the tibia was taken for micro-CT examination of bone mineral density (BMD) and bone volume/structural parameters (BV/TV), while the femur was taken for the measurement of absorption parameters (Ob.S)./BS) and the number of osteoclasts per circumference of bone (N.Oc/B.Pm).

RESULTS

The expression level of miR-203 was significantly lower in patients with postmenopausal osteoporosis than that in normal individuals. The osteogenic capacity of BMSCs in these patients was reduced, while their adipogenic capacity was enhanced. MiR-203 promoted the expression of osteogenic genes and inhibited that of adipogenic genes. Knockdown of miR-203 decreased the level of osteogenic related genes but increased that of adipogenic related genes, while overexpression of miR-203 led to the opposite results. Furthermore, miR-203 inhibited the protein expression of DKK1. In addition, bone density and bone volume/structural parameters were lower in ovariectomized rats than those in normal rats. Meanwhile, bone resorption parameters and the number of osteoclasts per bone circumference in ovariectomized rats were higher than those in normal rats.

CONCLUSIONS

MiR-203 can promote osteogenic differentiation of mesenchymal stem cells by downregulating the gene expression of DKK1.

摘要

目的

本研究旨在通过调节其靶基因 DKK1 来研究 miR-203 如何促进骨髓间充质细胞(BMSCs)的成骨分化,从而抑制骨质疏松症的发生。

方法

共纳入 60 例绝经后骨质疏松症患者和 40 例正常个体。采用实时定量逆转录聚合酶链反应(qRT-PCR)检测所有患者血清中 miR-203 的表达。通过茜素红染色和油红染色分别测定 MSC 的成骨和成脂分化能力。通过脂质体介导 miR-203 模拟物和 miR-203 抑制剂的转染,然后诱导 MSC 成骨和成脂分化。miR-203 模拟物与野生型或突变型 DKK1 共转染用于荧光素酶报告基因检测。在大鼠骨质疏松模型中,取胫骨进行骨矿物质密度(BMD)和骨体积/结构参数(BV/TV)的 micro-CT 检查,取股骨进行吸收参数(Ob.S)/BS)和骨周破骨细胞数(N.Oc/B.Pm)的测量。

结果

绝经后骨质疏松症患者 miR-203 的表达水平明显低于正常个体。这些患者的 BMSCs 成骨能力降低,而成脂能力增强。miR-203 促进成骨基因的表达,抑制成脂基因的表达。miR-203 敲低降低了成骨相关基因的水平,但增加了成脂相关基因的水平,而过表达 miR-203 则导致相反的结果。此外,miR-203 抑制了 DKK1 蛋白的表达。此外,去卵巢大鼠的骨密度和骨体积/结构参数低于正常大鼠。同时,去卵巢大鼠的骨吸收参数和每骨周破骨细胞数高于正常大鼠。

结论

miR-203 可通过下调 DKK1 基因表达促进间充质干细胞的成骨分化。

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