Expansion of Chondrocytes for Cartilage Tissue Engineering: A Review of Chondrocyte Dedifferentiation and Redifferentiation as a Function of Growth in Expansion Culture

J. Kisiday
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引用次数: 7

Abstract

Culture-expansion is a common step in the use of autologous chondrocytes for cartilage tissue engineering. Chondrocytes dedifferentiate in monolayer expansion culture, and conditions that are sufficient to induce redifferentiation change as a function of cumulative growth. The objective of this review was to characterize the relationship between expansion and redifferentiation, from which requirements to induce redifferentiation were identified for selected approaches to cartilage tissue engineering. While chondrocytes dedifferentiate rapidly in expansion culture, transferring the cells to a three-dimensional scaffold is sufficient to induce redifferentiation for up to ~6 population doublings (PDs). Redifferentiation is possible beyond 6 PDs, although exposure to chondrogenic cytokines is needed. These data indicate that dedifferentiation with expansion for treating focal defects (~6 PDs) can be reversed with transfer to a scaffold, while joint resurfacing (~10 PDs) is anticipated to require exposure to chondrogenic cytokines. During expansion, growth factor supplementation can accelerate proliferation and improve redifferentiation. However, redifferentiation may require chondrogenic cytokines, and should be considered for approaches that involve expansion beyond the limit for spontaneous redifferentiation.
软骨组织工程中软骨细胞的增殖:增殖培养中软骨细胞去分化和再分化的研究进展
培养扩增是使用自体软骨细胞进行软骨组织工程的常见步骤。软骨细胞在单层扩增培养中去分化,并且条件足以诱导作为累积生长函数的再分化变化。这篇综述的目的是描述扩张和再分化之间的关系,从中确定了软骨组织工程选择方法诱导再分化的要求。当软骨细胞在扩增培养中快速去分化时,将细胞转移到三维支架上足以诱导多达6个群体加倍(PD)的再分化。尽管需要暴露于软骨生成细胞因子,但6个PDs之后的再分化是可能的。这些数据表明,用于治疗局灶性缺陷的去分化和扩张(~6个PDs)可以通过转移到支架上逆转,而关节表面重建(~10个PDs)预计需要暴露于软骨生成细胞因子。在扩增过程中,补充生长因子可以加速增殖并改善再分化。然而,再分化可能需要软骨生成细胞因子,并且应该考虑用于涉及超出自发再分化极限的扩增的方法。
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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