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在具有免疫活性的实验动物模型中,由广泛扩增的软骨细胞构建的耳状稳定耳廓软骨

Ear-Shaped Stable Auricular Cartilage Engineered from Extensively Expanded Chondrocytes in an Immunocompetent Experimental Animal Model.

作者信息

Pomerantseva Irina, Bichara David A, Tseng Alan, Cronce Michael J, Cervantes Thomas M, Kimura Anya M, Neville Craig M, Roscioli Nick, Vacanti Joseph P, Randolph Mark A, Sundback Cathryn A

机构信息

1 Department of Surgery, Massachusetts General Hospital , Boston, Massachusetts.

2 Harvard Medical School , Boston, Massachusetts.

出版信息

Tissue Eng Part A. 2016 Feb;22(3-4):197-207. doi: 10.1089/ten.TEA.2015.0173. Epub 2015 Dec 15.

Abstract

Advancement of engineered ear in clinical practice is limited by several challenges. The complex, largely unsupported, three-dimensional auricular neocartilage structure is difficult to maintain. Neocartilage formation is challenging in an immunocompetent host due to active inflammatory and immunological responses. The large number of autologous chondrogenic cells required for engineering an adult human-sized ear presents an additional challenge because primary chondrocytes rapidly dedifferentiate during in vitro culture. The objective of this study was to engineer a stable, human ear-shaped cartilage in an immunocompetent animal model using expanded chondrocytes. The impact of basic fibroblast growth factor (bFGF) supplementation on achieving clinically relevant expansion of primary sheep chondrocytes by in vitro culture was determined. Chondrocytes expanded in standard medium were either combined with cryopreserved, primary passage 0 chondrocytes at the time of scaffold seeding or used alone as control. Disk and human ear-shaped scaffolds were made from porous collagen; ear scaffolds had an embedded, supporting titanium wire framework. Autologous chondrocyte-seeded scaffolds were implanted subcutaneously in sheep after 2 weeks of in vitro incubation. The quality of the resulting neocartilage and its stability and retention of the original ear size and shape were evaluated at 6, 12, and 20 weeks postimplantation. Neocartilage produced from chondrocytes that were expanded in the presence of bFGF was superior, and its quality improved with increased implantation time. In addition to characteristic morphological cartilage features, its glycosaminoglycan content was high and marked elastin fiber formation was present. The overall shape of engineered ears was preserved at 20 weeks postimplantation, and the dimensional changes did not exceed 10%. The wire frame within the engineered ear was able to withstand mechanical forces during wound healing and neocartilage maturation and prevented shrinkage and distortion. This is the first demonstration of a stable, ear-shaped elastic cartilage engineered from auricular chondrocytes that underwent clinical-scale expansion in an immunocompetent animal over an extended period of time.

摘要

工程化耳朵在临床实践中的进展受到若干挑战的限制。复杂的、大多无支撑的三维耳廓新软骨结构难以维持。由于活跃的炎症和免疫反应,在具有免疫活性的宿主体内形成新软骨具有挑战性。构建成人尺寸耳朵所需的大量自体软骨生成细胞带来了额外挑战,因为原代软骨细胞在体外培养过程中会迅速去分化。本研究的目的是在具有免疫活性的动物模型中,使用扩增的软骨细胞构建稳定的人耳形状软骨。确定了补充碱性成纤维细胞生长因子(bFGF)对通过体外培养实现原代绵羊软骨细胞临床相关扩增的影响。在支架接种时,将在标准培养基中扩增的软骨细胞与冷冻保存的原代第0代传代软骨细胞混合,或单独用作对照。圆盘和人耳形状的支架由多孔胶原蛋白制成;耳支架有一个嵌入的支撑钛丝框架。体外培养2周后,将自体软骨细胞接种的支架皮下植入绵羊体内。在植入后6周、12周和20周评估所得新软骨的质量及其稳定性以及原始耳朵大小和形状的保持情况。在bFGF存在下扩增的软骨细胞产生的新软骨更优,其质量随植入时间增加而改善。除了具有特征性的形态学软骨特征外,其糖胺聚糖含量高且有明显的弹性纤维形成。工程化耳朵的整体形状在植入后20周得以保留,尺寸变化不超过10%。工程化耳朵内的金属丝框架能够在伤口愈合和新软骨成熟过程中承受机械力,并防止收缩和变形。这是首次证明从耳廓软骨细胞构建的稳定的耳状弹性软骨在具有免疫活性的动物体内经过临床规模的扩增并持续了较长时间。

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