电诱导人间充质干细胞促进骨软骨缺损再生的成软骨分化。

IF 8.1 Q1 ENGINEERING, BIOMEDICAL
Biomaterials research Pub Date : 2024-12-18 eCollection Date: 2024-01-01 DOI:10.34133/bmr.0109
Jongdarm Yi, Yujin Byun, Seong Soo Kang, Kyung Mi Shim, Kwangsik Jang, Jae Young Lee
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引用次数: 0

摘要

背景:间充质干细胞(MSCs)为软骨再生提供了一条很有前途的途径;然而,它们的治疗效果需要大幅度提高。使用电刺激(ES)的细胞启动是一种很有前途的方法来增强间充质干细胞的治疗潜力,并显示出各种再生应用的潜力。本研究旨在促进es介导的人间充质干细胞成软骨分化,促进损伤关节软骨的修复。方法:对MSCs在不同条件下(如电压、频率、重复次数)进行ES培养,增强其软骨形成和软骨再生能力。通过基因表达和硫代糖胺聚糖生成来评估电诱导的间充质干细胞(epMSCs)的成软骨分化,并将加入透明质酸的epMSCs移植到大鼠骨软骨缺损模型中。通过ES进行转录组学分析以确定基因表达的变化。结果:与未受刺激的对照组相比,epMSCs表现出显著增加的软骨基因表达和硫酸糖胺聚糖的产生。肉眼和组织学结果显示,epMSC在体内移植可显著促进软骨再生。此外,ES显著改变了MSCs中许多基因的表达,包括与细胞外基质、Wnt信号通路和软骨发育相关的基因。结论:ES能有效激活MSCs促进关节软骨修复,为提高各种MSCs治疗的疗效提供了一种有希望的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhanced Chondrogenic Differentiation of Electrically Primed Human Mesenchymal Stem Cells for the Regeneration of Osteochondral Defects.

Background: 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. Methods: 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. Results: 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. Conclusion: ES can effectively prime MSCs to improve articular cartilage repair, offering a promising strategy for enhancing the efficacy of various MSC-based therapies.

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