人类软骨微组织的成熟状态和密度影响了它们的融合和发展成为扩大规模的移植
Francesca D Spagnuolo1, Gabriela S Kronemberger1, Kyle J Storey1
1Trinity Centre for Biomedical Engineering, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin, Ireland; Department of Mechanical, Manufacturing and Biomedical Engineering, School of Engineering, Trinity College Dublin, Dublin, Ireland.
Acta biomaterialia
|January 16, 2025
概括
使用不太成熟的软骨微组织 (μTs) 促进更快的融合和更好的细胞外基质发育工程移植. 缩放到4000μTs显示强大的融合,支持大规模的软骨组织工程.
科学领域:
- 生物材料科学 生物材料科学
- 组织工程是组织工程.
- 再生医学是一种再生医学.
背景情况:
- 微组织 (μT) 是工程功能性软骨组织的关键组成部分.
- 微晶体的成熟程度会影响其融合能力,但对工程组织的长期影响尚不清楚.
研究的目的:
- 研究人类骨髓介质干细胞/骨干细胞 (hBM-MSCs) 微组织成熟如何影响融合和工程组织表型.
- 优化扩大微组织融合的策略,以促进大软骨移植的发展.
主要方法:
- 较为成熟的hBM-MSC微组织与较为成熟的hBM-MSC微组织相比,较不成熟 (2日) 的融合和矩阵发育.
- 使用不同数量的 (50-300) 较不成熟的微组织,设计了更大的结构.
- 缩放到4000个微组织,并在静态或动态条件下培养.
主要成果:
- 较不成熟的微组织更快地融合,产生富含硫酸氨基甘油 (sGAG) 和较少的原的矩阵.
- 增加微组织密度增强了sGAG合成.
- 4000个微组织强烈融合;动态培养对矩阵积累或拉伸模量没有明显的优势.
结论:
- 较不成熟的hBM-MSCs微组织是工程软骨中强大的融合和基生成的最佳选择.
- 使用微组织融合的生物制造可扩展到临床相关的软骨移植大小.
- 这一策略支持大规模功能性软骨移植的发展.
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