Injectable cartilage microtissues based on 3D culture using porous gelatin microcarriers for cartilage defect treatment.

IF 5.6 1区 医学 Q1 MATERIALS SCIENCE, BIOMATERIALS
Regenerative Biomaterials Pub Date : 2024-06-04 eCollection Date: 2024-01-01 DOI:10.1093/rb/rbae064
Jing Zhu, Qiuchen Luo, Tiefeng Cao, Guang Yang, Lin Xiao
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引用次数: 0

Abstract

Cartilage tissues possess an extremely limited capacity for self-repair, and current clinical surgical approaches for treating articular cartilage defects can only provide short-term relief. Despite significant advances in the field of cartilage tissue engineering, avoiding secondary damage caused by invasive surgical procedures remains a challenge. In this study, injectable cartilage microtissues were developed through 3D culture of rat bone marrow mesenchymal stem cells (BMSCs) within porous gelatin microcarriers (GMs) and induced differentiation. These microtissues were then injected for the purpose of treating cartilage defects in vivo, via a minimally invasive approach. GMs were found to be noncytotoxic and favorable for cell attachment, proliferation and migration evaluated with BMSCs. Moreover, cartilage microtissues with a considerable number of cells and abundant extracellular matrix components were obtained from BMSC-laden GMs after induction differentiation culture for 28 days. Notably, ATDC5 cells were complementally tested to verify that the GMs were conducive to cell attachment, proliferation, migration and chondrogenic differentiation. The microtissues obtained from BMSC-laden GMs were then injected into articular cartilage defect areas in rats and achieved superior performance in alleviating inflammation and repairing cartilage. These findings suggest that the use of injectable cartilage microtissues in this study may hold promise for enhancing the long-term outcomes of cartilage defect treatments while minimizing the risk of secondary damage associated with traditional surgical techniques.

基于多孔明胶微载体三维培养的可注射软骨微组织,用于软骨缺损治疗。
软骨组织的自我修复能力极其有限,目前治疗关节软骨缺损的临床手术方法只能提供短期缓解。尽管软骨组织工程领域取得了重大进展,但避免侵入性手术造成二次损伤仍是一项挑战。在这项研究中,通过在多孔明胶微载体(GMs)中对大鼠骨髓间充质干细胞(BMSCs)进行三维培养并诱导分化,开发出了可注射的软骨微组织。然后将这些微组织注入体内,通过微创方法治疗软骨缺损。通过对 BMSCs 的评估发现,GMs 无细胞毒性,有利于细胞附着、增殖和迁移。此外,经过 28 天的诱导分化培养后,含有大量细胞和丰富细胞外基质成分的 BMSC 基因改造体获得了软骨微组织。值得注意的是,对 ATDC5 细胞进行了互补测试,以验证转基因有利于细胞的附着、增殖、迁移和软骨分化。然后,将从含有 BMSC 的基因改造体中获得的微组织注射到大鼠的关节软骨缺损区,在缓解炎症和修复软骨方面取得了卓越的效果。这些发现表明,本研究中使用的可注射软骨微组织有望提高软骨缺损治疗的长期效果,同时最大限度地降低传统手术技术带来的二次损伤风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Regenerative Biomaterials
Regenerative Biomaterials Materials Science-Biomaterials
CiteScore
7.90
自引率
16.40%
发文量
92
审稿时长
10 weeks
期刊介绍: Regenerative Biomaterials is an international, interdisciplinary, peer-reviewed journal publishing the latest advances in biomaterials and regenerative medicine. The journal provides a forum for the publication of original research papers, reviews, clinical case reports, and commentaries on the topics relevant to the development of advanced regenerative biomaterials concerning novel regenerative technologies and therapeutic approaches for the regeneration and repair of damaged tissues and organs. The interactions of biomaterials with cells and tissue, especially with stem cells, will be of particular focus.
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