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使用传代猪软骨细胞和碱性成纤维细胞生长因子的无支架软骨制造系统

Scaffold-free cartilage fabrication system using passaged porcine chondrocytes and basic fibroblast growth factor.

作者信息

Jin Ri Long, Park So Ra, Choi Byung Hyune, Min Byoung-Hyun

机构信息

Department of Orthopaedic Surgery, School of Medicine, Ajou University , Suwon, Republic of Korea .

出版信息

Tissue Eng Part A. 2009 Aug;15(8):1887-95. doi: 10.1089/ten.tea.2008.0349.

DOI:10.1089/ten.tea.2008.0349
PMID:19132891
Abstract

The scaffold-free cartilage fabrication system we have reported previously for human application with nonpassaged cells has a big limitation in securing the enough cell number. Therefore, autologous chondrocytes from small biopsy of cartilage tissue inevitably have to be expanded through multiple passages, which result in poor engineered cartilage in terms of quality and quantity. This study applied basic fibroblast growth factor (bFGF) to overcome the limitation and produce an engineered cartilage tissue with clinically applicable size and quality. Porcine articular chondrocytes were expanded until passage 2 in the absence or presence of 5 ng/mL bFGF, and then subjected to the two-stage scaffold-free cultures for 21 days again in the absence or presence of 5 ng/mL bFGF. The fabrication of cartilage tissues was evaluated along with time in comparison with the constructs from unpassaged chondrocytes. Expansion of chondrocytes in the presence of bFGF increased accumulation of cartilage extracellular matrices and resultantly fabricated the larger size of cartilage tissues in the subsequent stages, being comparable to those of unpassaged cells. In contrast, bFGF showed no positive, but adverse, effects on the cartilage tissue formation, when treated additionally during the scaffold-free fabrication stages. These results suggested that use of bFGF during the expansion stage of chondrocytes could overcome the limitation of previous two-stage scaffold-free cartilage fabrication system, and provided a novel three-stage system to construct a clinically applicable quality of cartilage tissues.

摘要

我们之前报道的用于人体应用的无支架软骨制造系统,使用未传代细胞时在确保足够细胞数量方面存在很大局限性。因此,从软骨组织小块活检中获取的自体软骨细胞不可避免地要经过多次传代扩增,这导致工程化软骨在质量和数量方面都很差。本研究应用碱性成纤维细胞生长因子(bFGF)来克服这一局限性,并制造出具有临床适用尺寸和质量的工程化软骨组织。将猪关节软骨细胞在不存在或存在5 ng/mL bFGF的情况下扩增至第2代,然后在不存在或存在5 ng/mL bFGF的情况下再次进行两阶段无支架培养21天。与未传代软骨细胞构建的组织相比,随时间评估软骨组织的制造情况。在bFGF存在下软骨细胞的扩增增加了软骨细胞外基质的积累,从而在后续阶段制造出更大尺寸的软骨组织,与未传代细胞的组织相当。相比之下,在无支架制造阶段额外添加bFGF时,对软骨组织形成没有积极作用,反而有不利影响。这些结果表明,在软骨细胞扩增阶段使用bFGF可以克服先前两阶段无支架软骨制造系统的局限性,并提供了一种构建具有临床适用质量软骨组织的新型三阶段系统。

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