School of Medicine, Sun Yat-sen University Guangzhou 510182, Guangdong Province, China ; Shenzhen Key Laboratory of Tissue Engineering, Shenzhen Second People's Hospital Shenzhen 518035, Guangdong Province, China ; Department of Orthopedics, Shenzhen Second People's Hospital Shenzhen 518035, Guangdong Province, China.
Division of Immunology, University Children's Hospital Zurich Zurich 8032, Switzerland.
Am J Transl Res. 2015 Feb 15;7(2):194-208. eCollection 2015.
Autologous chondrocyte implantation (ACI) is a golden treatment for large defects of the knee joint without osteoarthritis or other complications. Despite notable progresses, generation of a stable chondrocyte phenotype using progenitor cells remains a main obstacle for chondrocyte-based cartilage treatment. Monolayer chondrocyte expansion in vitro is accompanied by chondrocyte dedifferentiation, which produces a non-specific mechanically inferior extracellular matrix (ECM) unsuitable for ACI. In-depth understanding of the molecular events during chondrocyte dedifferentiation is required to maintain the capacity of in vitro expanded chondrocytes to produce hyaline cartilage-specific ECM. This review discusses key cytokines and signaling pathways involved in chondrocyte dedifferentiation from the standpoint of catabolism and anabolism. Some potential therapeutic strategies are also presented to counteract chondrocyte dedifferentiation for cell-based cartilage therapy.
自体软骨细胞移植(ACI)是治疗无骨关节炎或其他并发症的膝关节大缺损的黄金方法。尽管取得了显著进展,但使用祖细胞生成稳定的软骨细胞表型仍然是基于软骨细胞的软骨治疗的主要障碍。体外单层软骨细胞扩增伴随着软骨细胞去分化,产生不适合 ACI 的非特异性机械性能较差的细胞外基质(ECM)。为了维持体外扩增的软骨细胞产生透明软骨特异性 ECM 的能力,需要深入了解软骨细胞去分化过程中的分子事件。本文从分解代谢和合成代谢的角度讨论了参与软骨细胞去分化的关键细胞因子和信号通路。还提出了一些潜在的治疗策略来对抗细胞基软骨治疗中的软骨细胞去分化。