Yi Jongdarm, Byun Yujin, Kang Seong Soo, Shim Kyung Mi, Jang Kwangsik, Lee Jae Young
School of Materials Science and Engineering, Gwangju Institute of Science and Technology, Gwangju 61005, Republic of Korea.
Department of Veterinary Surgery, College of Veterinary Medicine and BK21 FOUR Program, Chonnam National University, Gwangju 61186, Republic of Korea.
Biomater Res. 2024 Dec 18;28:0109. doi: 10.34133/bmr.0109. eCollection 2024.
Mesenchymal stem cells (MSCs) offer a promising avenue for cartilage regeneration; however, their therapeutic efficacy requires substantial improvement. Cell priming using electrical stimulation (ES) is a promising approach to augmenting the therapeutic potential of MSCs and has shown potential for various regenerative applications. This study aimed to promote the ES-mediated chondrogenic differentiation of human MSCs and facilitate the repair of injured articular cartilage. MSCs were subjected to ES under various conditions (e.g., voltage, frequency, and number of repetitions) to enhance their capability of chondrogenesis and cartilage regeneration. Chondrogenic differentiation of electrically primed MSCs (epMSCs) was assessed based on gene expression and sulfated glycosaminoglycan production, and epMSCs with hyaluronic acid were transplanted into a rat osteochondral defect model. Transcriptomic analysis was performed to determine changes in gene expression by ES. epMSCs exhibited significantly increased chondrogenic gene expression and sulfated glycosaminoglycan production compared with those in unstimulated controls. Macroscopic and histological results showed that in vivo epMSC transplantation considerably enhanced cartilage regeneration. Furthermore, ES markedly altered the expression of numerous genes of MSCs, including those associated with the extracellular matrix, the Wnt signaling pathway, and cartilage development. ES can effectively prime MSCs to improve articular cartilage repair, offering a promising strategy for enhancing the efficacy of various MSC-based therapies.
间充质干细胞(MSCs)为软骨再生提供了一条有前景的途径;然而,它们的治疗效果需要大幅提高。使用电刺激(ES)对细胞进行预处理是增强MSCs治疗潜力的一种有前景的方法,并且已显示出在各种再生应用中的潜力。本研究旨在促进ES介导的人MSCs向软骨细胞分化,并促进受损关节软骨的修复。在各种条件(例如电压、频率和重复次数)下对MSCs进行ES处理,以增强其软骨形成和软骨再生能力。基于基因表达和硫酸化糖胺聚糖的产生来评估经电预处理的MSCs(epMSCs)的软骨形成分化,并将含有透明质酸的epMSCs移植到大鼠骨软骨缺损模型中。进行转录组分析以确定ES引起的基因表达变化。与未刺激的对照组相比,epMSCs表现出显著增加的软骨形成基因表达和硫酸化糖胺聚糖产生。宏观和组织学结果表明,体内epMSC移植显著增强了软骨再生。此外,ES显著改变了MSCs众多基因的表达,包括那些与细胞外基质、Wnt信号通路和软骨发育相关的基因。ES可以有效地预处理MSCs以改善关节软骨修复,为提高各种基于MSCs的治疗效果提供了一种有前景的策略。