研究人体软骨修复中新软骨和整合的动态加载体外模型。

IF 4.6 2区 生物学 Q2 CELL BIOLOGY
Frontiers in Cell and Developmental Biology Pub Date : 2024-09-30 eCollection Date: 2024-01-01 DOI:10.3389/fcell.2024.1449015
Anna Trengove, Lilith M Caballero Aguilar, Claudia Di Bella, Carmine Onofrillo, Serena Duchi, Andrea J O'Connor
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引用次数: 0

摘要

膝关节软骨损伤如不及时治疗,可能会导致创伤后骨关节炎,给患者日后的生活带来严重影响。标准的手术治疗无法确保对受损软骨进行长期持久的修复,往往会导致纤维组织的形成。虽然对软骨再生进行了大量研究,但将工程植入物与软骨结合仍是一项挑战。软骨是一种承重组织,因此必须评估组织修复策略及其在机械负荷下的整合能力。这项研究利用人体软骨外植体建立了动态加载的软骨修复体外模型。该模型用于评估干细胞疗法在由光交联甲基丙烯酰明胶(GelMA)和微生物转谷氨酰胺酶组成的生物粘性水凝胶中的疗效,以修复模型缺损。经过 28 天的软骨培养后,通过组织学和免疫组化观察到了广泛的新软骨生成和整合。通过对培养基的分析,可以监测糖胺聚糖和 II 型胶原蛋白随时间推移的生成情况。通过推出试验对整合进行的力学评估显示,在培养期间,推出强度增加了 15 倍。无论是否使用转谷氨酰胺酶,在两种培养条件下,该模型都能成功地表现出稳健的软骨生成。这项工作还强调了体内外模型的一些局限性以及使用生物反应器工作所面临的挑战,要提高这些模型的实用性,就必须克服这些挑战。这种体外模型有可能推迟昂贵的临床前研究,并对软骨修复策略进行比体内更细致的评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A dynamically loaded ex vivo model to study neocartilage and integration in human cartilage repair.

Articular cartilage injuries in the knee can lead to post-traumatic osteoarthritis if untreated, causing debilitating problems later in life. Standard surgical treatments fail to ensure long lasting repair of damaged cartilage, often resulting in fibrotic tissue. While there is a vast amount of research into cartilage regeneration, integrating engineered implants with cartilage remains a challenge. As cartilage is a load bearing tissue, it is imperative to evaluate tissue repair strategies and their ability to integrate under mechanical loading. This work established a dynamically loaded ex vivo model of cartilage repair using human cartilage explants. The model was used to assess the efficacy of a stem cell therapy delivered in a bioadhesive hydrogel comprised of photocrosslinkable gelatin methacryloyl (GelMA) and microbial transglutaminase to repair the model defect. Extensive neocartilage production and integration were observed via histology and immunohistochemistry after 28 days chondrogenic culture. Analysis of culture media allowed monitoring of glycosaminoglycan and type II collagen production over time. A mechanical assessment of integration via a push out test showed a 15-fold increase in push out strength over the culture duration. The model was successful in exhibiting robust chondrogenesis with transglutaminase or without, and under both culture conditions. The work also highlights several limitations of ex vivo models and challenges of working with bioreactors that must be overcome to increase their utility. This ex vivo model has the potential to delay the need for costly pre-clinical studies and provide a more nuanced assessment of cartilage repair strategies than is possible in vivo.

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来源期刊
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
9.70
自引率
3.60%
发文量
2531
审稿时长
12 weeks
期刊介绍: Frontiers in Cell and Developmental Biology is a broad-scope, interdisciplinary open-access journal, focusing on the fundamental processes of life, led by Prof Amanda Fisher and supported by a geographically diverse, high-quality editorial board. The journal welcomes submissions on a wide spectrum of cell and developmental biology, covering intracellular and extracellular dynamics, with sections focusing on signaling, adhesion, migration, cell death and survival and membrane trafficking. Additionally, the journal offers sections dedicated to the cutting edge of fundamental and translational research in molecular medicine and stem cell biology. With a collaborative, rigorous and transparent peer-review, the journal produces the highest scientific quality in both fundamental and applied research, and advanced article level metrics measure the real-time impact and influence of each publication.
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