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重组胶原基质对小鼠胚胎干细胞诱导软骨分化前后细胞命运的影响。

Effects of reconstituted collagen matrix on fates of mouse embryonic stem cells before and after induction for chondrogenic differentiation.

作者信息

Yeung Chiu W, Cheah Kathryn, Chan Danny, Chan Barbara P

机构信息

Medical Engineering Program, Department of Mechanical Engineering, The University of Hong Kong, Hong Kong Special Administrative Region, China.

出版信息

Tissue Eng Part A. 2009 Oct;15(10):3071-85. doi: 10.1089/ten.TEA.2008.0661.

Abstract

Embryonic stem (ES) cells are pluripotent cells with great potential in regenerative medicine. However, controlling their differentiation toward homogeneous lineages is challenging. In this study, we aim to investigate the effects of reconstituted 3D collagen matrix on the fates of mouse ES (mES) cells before and after induction for chondrogenic differentiation. Specifically, mES cells were encapsulated and cultured in 3D collagen microspheres and exposed to induction signals at different time points. Growth characteristics and differentiation status of mES cells were then evaluated. Collagen microspheres provided a suitable microenvironment supporting mES cell growth and maintaining their undifferentiated status for certain period of time. At later time points, the proportion of undifferentiated mES cells gradually decreased, accompanied by increasing proportions of mesenchymal progenitor cells. This suggests the inductive role of collagen matrix in differentiating mES cells toward mesenchymal lineages. Moreover, a lower initial collagen monomer concentration facilitated the differentiation of mES cells into chondrogenic lineages, while induction at a later time point associated with a more advanced stage of chondrogenic differentiation. This indicates that both the initial collagen concentration and the time to induce differentiation significantly affected the fates of mES cells. This study contributes to future development of ES cell-based therapies.

摘要

胚胎干细胞(ES细胞)是具有再生医学巨大潜力的多能干细胞。然而,控制它们向同质谱系分化具有挑战性。在本研究中,我们旨在研究重组3D胶原基质对小鼠ES(mES)细胞软骨分化诱导前后细胞命运的影响。具体而言,将mES细胞封装在3D胶原微球中并培养,在不同时间点给予诱导信号。然后评估mES细胞的生长特性和分化状态。胶原微球提供了一个合适的微环境,支持mES细胞生长并在一定时间内维持其未分化状态。在后期时间点,未分化mES细胞的比例逐渐降低,同时间充质祖细胞的比例增加。这表明胶原基质在促使mES细胞向间充质谱系分化中具有诱导作用。此外,较低的初始胶原单体浓度有利于mES细胞向软骨谱系分化,而在与软骨分化更高级阶段相关的后期时间点进行诱导。这表明初始胶原浓度和诱导分化的时间均显著影响mES细胞的命运。本研究有助于基于ES细胞的治疗方法的未来发展。

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