Effective repair of articular cartilage using human pluripotent stem cell-derived tissue.

IF 3.2 3区 医学 Q3 CELL & TISSUE ENGINEERING
O F Gardner, S C Juneja, H Whetstone, Y Nartiss, J T Sieker, C Veillette, G M Keller, A M Craft
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引用次数: 8

Abstract

In an effort to develop an effective source of clinically relevant cells and tissues for cartilage repair a directed differentiation method was used to generate articular chondrocytes and cartilage tissues from human embryonic stem cells (hESCs). It has previously been demonstrated that chondrocytes derived from hESCs retain a stable cartilage-forming phenotype following subcutaneous implantation in mice. In this report, the potential of hESC-derived articular-like cartilage to repair osteochondral defects created in the rat trochlea was evaluated. Articular cartilage-like tissues were generated from hESCs and implanted into the defects. After 6 and 12 weeks, the defects were evaluated histologically and immunohistochemically, and the quality of repair was assessed using a modified ICRS II scoring system. Following 6 and 12 weeks after implantation, hESC-derived cartilage tissues maintained their proteoglycan and type II collagen-rich matrix and scored significantly higher than control defects, which had been filled with fibrin glue alone. Implants were found to be well integrated with native host tissue at the basal and lateral surfaces, although implanted human cells and host cells remained regionally separated. A subset of implants underwent a process of remodeling similar to endochondral ossification, suggesting the potential for a single cartilaginous implant to promote the generation of new subchondral bone in addition to repair of the articular cartilage. The ability to create cartilage tissues with integrative and reparative properties from an unlimited and robust cell source represents a significant advance for cartilage repair that can be further developed in large animal models before clinical- setting application.

利用人多能干细胞衍生组织有效修复关节软骨。
为了开发软骨修复临床相关细胞和组织的有效来源,采用定向分化方法从人胚胎干细胞(hESCs)中生成关节软骨细胞和软骨组织。先前已经证明,hESCs衍生的软骨细胞在小鼠皮下植入后保持稳定的软骨形成表型。在本报告中,我们评估了hesc衍生的关节样软骨修复大鼠滑车骨软骨缺损的潜力。利用hESCs生成关节软骨样组织并植入缺损。6周和12周后,对缺损进行组织学和免疫组织化学评估,并使用改进的ICRS II评分系统评估修复质量。植入后6周和12周,hesc来源的软骨组织保持其蛋白多糖和II型胶原丰富基质,得分明显高于单独填充纤维蛋白胶的对照缺陷。虽然植入的人类细胞和宿主细胞仍然存在区域分离,但植入物在基底和外侧表面与宿主组织结合良好。一小部分植入物经历了类似软骨内成骨的重塑过程,这表明单个软骨植入物除了修复关节软骨外,还可能促进新的软骨下骨的生成。从无限和强大的细胞来源中创造具有整合和修复特性的软骨组织的能力代表了软骨修复的重大进步,可以在临床应用之前在大型动物模型中进一步发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European cells & materials
European cells & materials 生物-材料科学:生物材料
CiteScore
6.00
自引率
6.50%
发文量
55
审稿时长
1.5 months
期刊介绍: eCM provides an interdisciplinary forum for publication of preclinical research in the musculoskeletal field (Trauma, Maxillofacial (including dental), Spine and Orthopaedics). The clinical relevance of the work must be briefly mentioned within the abstract, and in more detail in the paper. Poor abstracts which do not concisely cover the paper contents will not be sent for review. Incremental steps in research will not be entertained by eCM journal.Cross-disciplinary papers that go across our scope areas are welcomed.
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