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软骨细胞三维包埋培养的进展:对组织工程和再生医学的启示。

Advancements in chondrocyte 3-dimensional embedded culture: Implications for tissue engineering and regenerative medicine.

作者信息

Chu Yu-Ying, Hikita Atsuhiko, Asawa Yukiyo, Hoshi Kazuto

机构信息

Department of Sensory and Motor System Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan; Department of Plastic and Reconstructive Surgery, Craniofacial Research Centre, Chang Gung Memorial Hospital at Linko, College of Medicine, Chang Gung University, Taoyuan, Taiwan.

Department of Tissue Engineering, The University of Tokyo Hospital, Tokyo, Japan.

出版信息

Biomed J. 2024 Sep 3;48(2):100786. doi: 10.1016/j.bj.2024.100786.

Abstract

Cartilage repair necessitates regenerative medicine because of the unreliable healing mechanism of cartilage. To yield a sufficient number of cells for transplantation, chondrocytes must be expanded in culture. However, in 2D culture, chondrocytes tend to lose their distinctive phenotypes and functionalities after serial passage, thereby limiting their efficacy for tissue engineering purposes. The mechanism of dedifferentiation in 2D culture can be attributed to various factors, including abnormal nuclear strength, stress-induced mitochondrial impairment, chromatin remodeling, ERK-1/2 and the p38/mitogen-activated protein kinase (MAPK) signaling pathway. These mechanisms collectively contribute to the loss of chondrocyte phenotype and reduced production of cartilage-specific extracellular matrix (ECM) components. Chondrocyte 3D culture methods have emerged as promising solutions to prevent dedifferentiation. Techniques, such as scaffold-based culture and scaffold-free approaches, provide chondrocytes with a more physiologically relevant environment, promoting their differentiation and matrix synthesis. These methods have been used in cartilage tissue engineering to create engineered cartilage constructs for transplantation and joint repair. However, chondrocyte 3D culture still has limitations, such as low viability and proliferation rate, and also difficulties in passage under 3D condition. These indicate challenges of obtaining a sufficient number of chondrocytes for large-scale tissue production. To address these issues, ongoing studies of many research groups have been focusing on refining culture conditions, optimizing scaffold materials, and exploring novel cell sources such as stem cells to enhance the quality and quantity of engineered cartilage tissues. Although obstacles remain, continuous endeavors to enhance culture techniques and overcome limitations offer a promising outlook for the advancement of more efficient strategies for cartilage regeneration.

摘要

由于软骨的愈合机制不可靠,软骨修复需要再生医学。为了获得足够数量的用于移植的细胞,软骨细胞必须在培养中进行扩增。然而,在二维培养中,软骨细胞在连续传代后往往会失去其独特的表型和功能,从而限制了它们在组织工程中的效用。二维培养中去分化的机制可归因于多种因素,包括异常的核强度、应激诱导的线粒体损伤、染色质重塑、ERK-1/2和p38/丝裂原活化蛋白激酶(MAPK)信号通路。这些机制共同导致软骨细胞表型的丧失和软骨特异性细胞外基质(ECM)成分的产生减少。软骨细胞三维培养方法已成为防止去分化的有前景的解决方案。基于支架的培养和无支架方法等技术为软骨细胞提供了更生理相关的环境,促进其分化和基质合成。这些方法已用于软骨组织工程,以创建用于移植和关节修复的工程化软骨构建体。然而,软骨细胞三维培养仍然存在局限性,如低活力和增殖率,以及在三维条件下传代困难。这些表明在大规模组织生产中获得足够数量的软骨细胞存在挑战。为了解决这些问题,许多研究小组正在进行的研究一直专注于优化培养条件、优化支架材料以及探索干细胞等新型细胞来源,以提高工程化软骨组织的质量和数量。尽管障碍仍然存在,但不断努力改进培养技术和克服局限性为推进更有效的软骨再生策略提供了有希望的前景。

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