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Chondrocytes-derived exosomal miR-8485 regulated the Wnt/beta-catenin pathways to promote chondrogenic differentiation of BMSCs

机译:软骨细胞衍生的外泌体miR-8485调节WNT /β-连环蛋白途径,以促进BMSC的软骨形成分化

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In indirect co-culture system, chondrocytes can induce differentiation of bone marrow mesenchymal stem cells (BMSCs) to chondrocytes without additional inducer. The participation of microRNAs (miRNAs) may take part in the chondrogenic differentiation. Present study aimed to investigate the effect and mechanism of chondrocytes-derived exosomal miRNA in BMSCs chondrogenic differentiation. Our data showed that miR-8485 was the exosomal miRNA derived from chondrocytes and transmitted to BMSCs. Functionally, miR-8485 silence in chondrocytes impaired exosome-induced chondrogenic differentiation of BMSCs. Mechanistically, exosomal miR-8485 targeted GSK3B to repress GSK-3 beta expression and targeted DACT1 to induce p-GSK-3 beta (Ser9), activating Wnt/beta catenin pathways. Our study firstly showed that chondrocytes-derived exosomal miR-8485 regulated the Wnt/beta-catenin pathways to promote chondrogenic differentiation of BMSCs, providing innovative thoughts for cartilage reconstruction. (C) 2019 Elsevier Inc. All rights reserved.
机译:在间接共培养系统中,软骨细胞可以诱导骨髓间充质干细胞(BMSCs)对软骨细胞的分化,而无需额外的诱导剂。 MicroRNAS(miRNA)的参与可能参与有软骨生分化。目前的研究旨在探讨软骨细胞衍生的新甲蛋白酶体MiRNA在BMSCs软骨形成分化中的效果和机制。我们的数据显示miR-8485是衍生自软骨细胞并传递给BMSCs的外泌体miRNA。在功能上,MIR-8485在软骨细胞中沉默受到BMSCs的外科诱导的软骨内分化。机械上,外泌体miR-8485靶向GSK3B,以压制GSK-3β表达和靶向DACT1以诱导P-GSK-3β(SER9),激活WNT /βCatenin途径。我们的研究首先表明,软骨细胞衍生的外泌胞miR-8485调节了WNT /β-连环蛋白途径,以促进BMSC的软骨性分化,为软骨重建提供创新思想。 (c)2019 Elsevier Inc.保留所有权利。

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