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褪黑素介导的 miR-526b-3p 和 miR-590-5p 的上调促进了人骨髓间充质干细胞的软骨分化。

Melatonin-mediated miR-526b-3p and miR-590-5p upregulation promotes chondrogenic differentiation of human mesenchymal stem cells.

机构信息

Department of Orthopedics, Sun Yat-sen Memorial Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China.

Department of Orthopedics, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China.

出版信息

J Pineal Res. 2018 Aug;65(1):e12483. doi: 10.1111/jpi.12483. Epub 2018 Mar 25.

Abstract

Bone marrow-derived mesenchymal stem cells (BMSCs), with inherent chondrogenic differentiation potential appear to be ideally suited for therapeutic use in cartilage regeneration. Accumulating evidence has demonstrated that melatonin can promote chondrogenic differentiation in human BMSCs. However, little is known about the mechanism. MicroRNAs (miRNAs) have been shown to regulate the differentiation of BMSCs, but their roles in melatonin-promoted chondrogenic differentiation have not been characterized. Here, we demonstrate that melatonin promoted chondrogenic differentiation of human BMSCs via upregulation of miR-526b-3p and miR-590-5p. Mechanistically, the elevated miR-526b-3p and miR-590-5p enhanced SMAD1 phosphorylation by targeting SMAD7. Additionally, administration of miR-526b-3p mimics or miR-590-5p mimics successfully promoted the chondrogenic differentiation of human BMSCs. Collectively, our study suggests that modification of BMSCs using melatonin or miRNA transduction could be an effective therapy for cartilage damage and degeneration.

摘要

骨髓间充质干细胞(BMSCs)具有内在的软骨分化潜能,似乎非常适合用于软骨再生的治疗。越来越多的证据表明褪黑素可以促进人 BMSCs 的软骨分化。然而,其机制知之甚少。microRNAs(miRNAs)已被证明可以调节 BMSCs 的分化,但它们在褪黑素促进软骨分化中的作用尚未得到描述。在这里,我们证明褪黑素通过上调 miR-526b-3p 和 miR-590-5p 促进人 BMSCs 的软骨分化。在机制上,升高的 miR-526b-3p 和 miR-590-5p 通过靶向 SMAD7 增强 SMAD1 的磷酸化。此外,miR-526b-3p 模拟物或 miR-590-5p 模拟物的给药成功地促进了人 BMSCs 的软骨分化。总之,我们的研究表明,使用褪黑素或 miRNA 转导修饰 BMSCs 可能是治疗软骨损伤和退变的有效方法。

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