Abstract

BackgroundIt is reported that miR-596 has a potential diagnostic value for non-traumatic osteonecrosis of the femoral head (NOFH), but its underlying mechanisms in NOFH is unclear.MethodsThe expression of miR-596 and Smad3 was detected by western blot and quantitative real-time PCR. The relationship between the two molecules was explored using Dual-Luciferase Reporter Assay. Glucocorticoid (GC)—dexamethasone, was used to induce bone marrow mesenchymal stem cell (BMSC) osteogenic differentiation, and the effects of miR-596 on BMSC osteogenic differentiation and proliferation were determined.ResultsMiR-596 expression was upregulated, while Smad3 expression was inhibited in the bone marrow samples of patients with steroid-induced osteonecrosis of femoral head (SANFH). Overexpression of miR-596 inhibited the proliferation and osteogenic differentiation of BMSCs induced by GC. Meanwhile, the opposite results were observed in the miR-596 inhibitor group. In addition, Smad3 was a target gene of miR-596, and negatively regulated by miR-596. The promotion effect of the miR-596 inhibitor on BMSC proliferation and osteogenic differentiation was reversed by si-Smad3.ConclusionMiR-596 can suppress GC-BMSC osteoblastic differentiation and proliferation by regulating Smad3 expression.

Highlights

  • It is reported that miR-596 has a potential diagnostic value for non-traumatic osteonecrosis of the femoral head (NOFH), but its underlying mechanisms in NOFH is unclear

  • These results indicated that miR-596 and Smad3 might be related with SANFH

  • MiR-596 expression was increased in GC-bone marrow mesenchymal stem cell (BMSC) we tested the expression of miR-596 in GCBMSCs

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Summary

Introduction

It is reported that miR-596 has a potential diagnostic value for non-traumatic osteonecrosis of the femoral head (NOFH), but its underlying mechanisms in NOFH is unclear. Bone marrow mesenchymal stem cells (BMSCs) are a group of stem cells with self-renewal and differentiation capabilities, which can differentiate into various cells, Fu et al Journal of Orthopaedic Surgery and Research (2020) 15:173 including adipocytes, chondrocytes, and osteoblasts [6]. It has been proved that the osteoblastic differentiation of BMSCs in SANFH is alleviated, but the fat differentiation is promoted [9]. The proliferation ability of BMSCs is reduced in patients with SANFH [10].

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