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A Puzzle Assembly Strategy for Fabrication of Large Engineered Cartilage Tissue Constructs

机译:大型工程软骨组织构造的拼图组装策略。

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摘要

Engineering of large articular cartilage tissue constructs remains a challenge as tissue growth is limited by nutrient diffusion. Here, a novel strategy is investigated, generating large constructs through the assembly of individually cultured, interlocking, smaller puzzle-shaped subunits. These constructs can be engineered consistently with more desirable mechanical and biochemical properties than larger constructs (~4-fold greater Young's modulus). A failure testing technique was developed to evaluate the physiologic functionality of constructs, which were cultured as individual subunits for 28 days, then assembled and cultured for an additional 21-35 days. Assembled puzzle constructs withstood large deformations (40-50% compressive strain) prior to failure. Their ability to withstand physiologic loads may be enhanced by increases in subunit strength and assembled culture time. A nude mouse model was utilized to show biocompatibility and fusion of assembled puzzle pieces in vivo. Overall, the technique offers a novel, effective approach to scaling up engineered tissues and may be combined with other techniques and/or applied to the engineering of other tissues. Future studies will aim to optimize this system in an effort to engineer and integrate robust subunits to fill large defects.
机译:大组织软骨组织构造的工程化仍然是一个挑战,因为组织的生长受到养分扩散的限制。在这里,研究了一种新颖的策略,通过单独培养的,互锁的,较小的拼图形状的亚基的组装来生成大型构建体。与更大的构建体(约4倍的杨氏模量)相比,可以对这些构建体进行一致的工程改造,使其具有更理想的机械和生化特性。开发了一种故障测试技术以评估构建体的生理功能,将其作为单个亚基培养28天,然后组装并培养21-35天。组装后的拼图结构在发生故障之前可以承受较大的变形(40-50%的压缩应变)。通过增加亚基强度和组装培养时间,可以提高它们承受生理负荷的能力。利用裸鼠模型显示生物相容性和体内组装拼图块的融合。总体而言,该技术提供了一种新颖,有效的方法来放大工程组织,并且可以与其他技术结合和/或应用于其他组织的工程。未来的研究将致力于优化该系统,以设计和集成强大的子单元来弥补大的缺陷。

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