Jang Jeongho, Lee Jungsun, Lee Eunkyung, Lee EunAh, Son Youngsook
Department of Genetic Engineering, College of Life Science, Kyung Hee University Global Campus, Yongin, Korea.
R&D Institute, MCTT Bio Inc., Seoul, Korea.
Tissue Eng Regen Med. 2016 Aug 5;13(4):352-363. doi: 10.1007/s13770-016-9065-6. eCollection 2016 Aug.
In this study, we developed the disc-type bio-cartilage reconstruction strategies for transplantable hyaline cartilage for reconstructive surgery using 3D-cell sheet culture of human bone marrow stromal cells and human costal chondrocytes. We compared chondrogenesis efficiency between different chondrogenic-induction methods such as micromass culture, pellet culture, and 3D-cell sheet culture. Among them, the 3D-cell sheet culture resulted in the best chondrogenesis with the disc-type bio-cartilage (>12 mm diameter in size) , but sometimes spontaneous curling and contraction of 3D-cell sheet culture resulted in the formation of bead-type cartilage, which was prevented by type I collagen coating or by culturing on amniotic membrane. Previously, it was reported that tissue-engineered cartilage reconstructed does not maintain its cartilage phenotype after transplantation but tends to transform to other tissue type such as bone or connective tissue. However, the disc-type bio-cartilage of 3D-cell sheet culture maintained its hyaline cartilage phenotype even after exposure to the osteogenic-induction condition for 3 weeks or after the transplantation for 4 weeks in mouse subcutaneous. Collectively, the disc-type bio-cartilage with 12 mm diameter can be reproducibly reconstructed by the 3D-cell sheet culture, whose hyaline cartilage phenotype and shape can be maintained under the osteogenic-induction condition as well as after the transplantation. This disc-type bio-cartilage can be proposed for the application to reconstructive surgery and repair of disc-type cartilage such as mandibular cartilage and digits.
Supplementary material is available for this article at 10.1007/s13770-016-9065-6 and is accessible for authorized users.
在本研究中,我们利用人骨髓基质细胞和人肋软骨细胞的三维细胞片层培养技术,开发了用于重建手术的可移植透明软骨的盘状生物软骨重建策略。我们比较了不同软骨诱导方法(如微团培养、颗粒培养和三维细胞片层培养)之间的软骨生成效率。其中,三维细胞片层培养法能生成最佳的软骨生成效果,形成直径大于12毫米的盘状生物软骨,但三维细胞片层培养有时会自发卷曲和收缩,导致形成珠状软骨,而通过I型胶原包被或在羊膜上培养可防止这种情况发生。此前有报道称,组织工程重建的软骨在移植后不能维持其软骨表型,而是倾向于转变为其他组织类型,如骨或结缔组织。然而,三维细胞片层培养的盘状生物软骨即使在成骨诱导条件下暴露3周或在小鼠皮下移植4周后,仍能维持其透明软骨表型。总体而言,直径为12毫米的盘状生物软骨可通过三维细胞片层培养可重复性重建,其透明软骨表型和形状在成骨诱导条件下以及移植后均可维持。这种盘状生物软骨可用于重建手术以及下颌软骨和手指等盘状软骨的修复。
本文的补充材料可在10.1007/s13770-016-9065-6获取,授权用户可访问。