Abstract

Cartilage injury of the knee joint is very common. Due to the limited self-healing ability of articular cartilage, osteoarthritis is very likely to occur if left untreated. Bone marrow mesenchymal stem cells (BMMSCs) are widely used in the study of cartilage injury due to their low immunity and good amplification ability, but they still have disadvantages, such as heterogeneous undifferentiated cells. MicroRNAs can regulate the chondrogenic differentiation ability of MSCs by inhibiting or promoting mRNA translation and degradation. In this research, we primarily investigated the effect of microRNA-210-3p (miR-210-3p) on chondrogenic and adipogenic differentiation of BMMSCs in vitro. Our results demonstrate that miR-210-3p promoted chondrogenic differentiation and inhibited adipogenic differentiation of rat BMMSCs, which was related to the HIF-3α signalling pathway. Additionally, miR-210-3p promotes mRNA and protein levels of the chondrogenic expression genes COLII and SOX9 and inhibits mRNA and protein levels of the adipogenic expression genes PPARγ and LPL. Thus, miR-210-3p combined with BMMSCs is a candidate for future clinical applications in cartilage regeneration and could represent a promising new therapeutic target for OA.

Highlights

  • Articular cartilage injury caused by trauma and arthritic diseases is one of the main causes of disability in middle-aged and elderly people [1]

  • We examined how miR-210 regulates chondrogenic differentiation of Bone marrow mesenchymal stem cells (BMMSCs)

  • We found that miR210 mimics actively promoted chondrogenic differentiation of BMMSCs

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Summary

Introduction

Articular cartilage injury caused by trauma and arthritic diseases is one of the main causes of disability in middle-aged and elderly people [1]. There are many ways to treat articular cartilage injury, and mesenchymal stem cells (MSCs) are widely studied due to their low immunogenicity, rapid amplification, and multidirectional differentiation. Many experimental data have indicated that miRNAs play a crucial regulatory role in the chondrogenic differentiation of MSCs [9,10,11]. By the regulation of specific genes, several miRNAs (miR-145 [12], miR-365 [13], and miR-218 [14]) have been shown to modulate chondrogenic differentiation of MSCs. miR-210 has been extensively studied and has many confirmed functional targets, such as cell proliferation, DNA damage response, angiogenesis, and apoptosis [15,16,17]. The participation of miR-2103p in BMMSC chondrogenic differentiation remains unclear. We investigated the effect of miR-210-3p on MSC chondrogenic and adipogenic differentiation

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