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克服工程大尺寸、无支架神经软骨的挑战,以获得功能性特性。

Overcoming Challenges in Engineering Large, Scaffold-Free Neocartilage with Functional Properties.

机构信息

1 Integrative Stem Cell Center, China Medical University Hospital , Taichung, Taiwan .

2 Institute of New Drug Development, China Medical University , Taichung, Taiwan .

出版信息

Tissue Eng Part A. 2018 Nov;24(21-22):1652-1662. doi: 10.1089/ten.TEA.2017.0495. Epub 2018 Jun 29.

DOI:10.1089/ten.TEA.2017.0495
PMID:29766751
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6238610/
Abstract

Although numerous cartilage engineering methods have been described, few report generation of constructs greater than 4 cm, which is the typical lesion size considered for cell-based therapies. Furthermore, current cell-based therapies only target focal lesions, while treatment of large nonisolated lesions remains an area of great demand. The objective of this study was to scale up fabrication of self-assembled neocartilage from standard sizes of 0.2 cm to greater than 8 cm. Passaged sheep articular chondrocytes were self-assembled into 5 or 25-mm-diameter scaffoldless neocartilage constructs. The 25-mm-diameter constructs grew up to 9.3 cm (areal scale-up of 23) and possessed properties similar to those of the 5-mm-diameter constructs; unfortunately, these large constructs were deformed and are unusable as a potential implant. A novel neocartilage fabrication strategy-employing mechanical confinement, a minute deadweight, and chemical stimulation (cytochalasin D, TGF-β1, chondroitinase-ABC, and lysyl oxidase-like 2 protein)-was found to successfully generate large (25-mm diameter) constructs with flat, homogeneous morphologies. Chemical stimulation increased collagen content and tensile Young's modulus 140% and 240% in the 25-mm-diameter constructs and 30% and 70% in the 5-mm-diameter constructs, respectively. This study not only demonstrated that exceedingly large self-assembled neocartilage can be generated with the appropriate combination of mechanical and chemical stimuli but also that its properties were maintained or even enhanced.

摘要

尽管已经描述了许多软骨工程方法,但很少有报道生成大于 4cm 的构建体,而这是细胞治疗中考虑的典型病变大小。此外,目前的基于细胞的治疗方法仅针对局灶性病变,而治疗大的非孤立性病变仍然是一个巨大的需求领域。本研究的目的是扩大自组装新软骨的制造规模,从标准的 0.2cm 增加到大于 8cm。传代的羊关节软骨细胞自组装成 5 或 25mm 直径无支架的新软骨构建体。25mm 直径的构建体生长到 9.3cm(面积放大 23 倍),并具有与 5mm 直径构建体相似的特性;不幸的是,这些大的构建体变形了,不能用作潜在的植入物。一种新的软骨制造策略——采用机械限制、微小的死重和化学刺激(细胞松弛素 D、TGF-β1、软骨素酶 ABC 和赖氨酰氧化酶样 2 蛋白)——被发现可以成功地制造出具有平坦、均匀形态的大(25mm 直径)构建体。化学刺激分别使 25mm 直径构建体中的胶原含量和拉伸杨氏模量增加了 140%和 240%,使 5mm 直径构建体中的胶原含量和拉伸杨氏模量增加了 30%和 70%。本研究不仅证明了通过适当的机械和化学刺激组合可以产生非常大的自组装新软骨,而且其性能得到了保持甚至增强。

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本文引用的文献

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A puzzle assembly strategy for fabrication of large engineered cartilage tissue constructs.一种用于制造大型工程化软骨组织构建体的拼图组装策略。
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