Department of Orthopaedics, The Affiliated Jiangning Hospital with Nanjing Medical University.
Department of Clinical Laboratory, The Affiliated Jiangning Hospital with Nanjing Medical University.
Biol Pharm Bull. 2022 Oct 1;45(10):1444-1451. doi: 10.1248/bpb.b22-00206. Epub 2022 Jul 20.
Cartilage regenerative medicine, wherein the stem cells from adults exert a crucial role, has high potential in the treatment of defective articular cartilage. Recently, Bone marrow mesenchymal stem cells (BMSCs) are being increasingly recognized as an alternative source of adult stem cells, which are capable of differentiating into several cell types (e.g., adipocytes, chondrocytes, and osteoblasts). However, their proliferative properties and tendency to dedifferentiate restrict their use in clinical settings. Recently, a possible bioactive material PRP-exos (exosomes derived from platelet-rich plasma), has emerged, which can effectively facilitate the differentiation and proliferation of cells. Recent studies have reported that berberine (Ber), known to have anti-inflammatory properties, plays a role in osteogenesis. Since biological molecules are used in combinations, we attempted to assess the effect of Exos-Ber (PRP-exos in combination with Ber) on the chondrogenic differentiation of BMSCs in vitro. In this study, Exos-Ber was observed to promote the proliferation of BMSCs and cause their chondrogenic differentiation in vitro. Additionally, Exos-Ber could promote the migration of BMSCs and increase the protein expression of the chondrogenic genes (Collagen II, SOX9, Aggrecan). After treatment with Exos-Ber, significant induction of β-catenin expression was observed, which could be repressed successfully by adding β-catenin inhibitor XAV-939. Interestingly, the repression of the Wnt/β-catenin axis also resulted in reduced gene expression levels of Collagen II, SOX9, and Aggrecan. These observations indicated that Exos-Ber facilitated the differentiation of chondrogenic BMSCs by modulating the Wnt/β-catenin axis, which offers innovative insights into the reconstruction of cartilage.
软骨再生医学中,成体干细胞起着至关重要的作用,在治疗有缺陷的关节软骨方面具有很大的潜力。最近,骨髓间充质干细胞(BMSCs)作为成体干细胞的另一种来源,越来越受到关注,它们能够分化为多种细胞类型(如脂肪细胞、软骨细胞和成骨细胞)。然而,其增殖特性和去分化倾向限制了其在临床中的应用。最近,一种可能的生物活性物质 PRP-exos(富含血小板的血浆衍生的外泌体)出现了,它可以有效地促进细胞的分化和增殖。最近的研究表明,具有抗炎特性的小檗碱(Ber)在成骨过程中发挥作用。由于生物分子是组合使用的,我们试图评估 Exos-Ber(PRP-exos 与 Ber 的组合)对 BMSCs 体外软骨分化的影响。在这项研究中,Exos-Ber 被观察到促进 BMSCs 的增殖,并在体外诱导其软骨分化。此外,Exos-Ber 可以促进 BMSCs 的迁移,并增加软骨基因(Collagen II、SOX9、Aggrecan)的蛋白表达。用 Exos-Ber 处理后,观察到β-catenin 的表达明显诱导,加入β-catenin 抑制剂 XAV-939 可成功抑制其表达。有趣的是,Wnt/β-catenin 轴的抑制也导致 Collagen II、SOX9 和 Aggrecan 的基因表达水平降低。这些观察结果表明,Exos-Ber 通过调节 Wnt/β-catenin 轴促进软骨源性 BMSCs 的分化,为软骨重建提供了新的见解。