基于功能化透明质酸水凝胶的软骨形成诱导系统依次促进hMSC增殖、凝聚、分化和基质沉积

Binhong Teng, Siqi Zhang, Jijia Pan, Ziqian Zeng, Yang Chen, Yu Hei, Xiaoming Fu, Qian Li, Mingyuan Ma, Yi Sui, Shicheng Wei
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引用次数: 28

摘要

水凝胶支架作为一种天然的干细胞生态位在软骨组织工程中得到了广泛的应用。特别是,基于多种生物信号的水凝胶可以指导间充质干细胞(MSCs)在新软骨形成过程中的行为。在本研究的第一阶段,我们发现带有精氨酸-甘氨酸-天冬氨酸(RGD)肽和低交联度的功能化水凝胶可以促进人间充质干细胞(hMSCs)的增殖并上调细胞受体蛋白的表达。此外,在水凝胶支架中移植RGD和组氨酸-丙氨酸-缬氨酸(HAV)肽可以在早期调节细胞间的粘附。在第二阶段,我们证实,与空白对照和单肽组相比,同时使用HAV和RGD肽可导致更大的软骨分化。此外,与其他组相比,kartogenin (KGN)的控释能更好地促进细胞软骨形成。有趣的是,随着培养时间的延长,RGD和HAV肽组的细胞明显凝结。在所有RGD肽组中,均观察到明显的基质沉积,并伴有糖胺聚糖(GAG)和胶原(Coll)的产生。本研究通过体外和体内实验证实,我们的水凝胶体系可以通过模拟新软骨形成过程中的细胞微环境,依次促进hMSCs的增殖、粘附、凝结、成软骨分化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Chondrogenesis Induction System Based on Functionalized Hyaluronic Acid Hydrogel Sequentially Promoting hMSC Proliferation, Condensation, and Differentiation and Matrix Deposition
Hydrogel scaffolds are widely used in cartilage tissue engineering as a natural stem cell niche. In particular, hydrogels based on multiple biological signals can guide behaviors of mesenchymal stem cells (MSCs) during neo-chondrogenesis. In the first phase of this study, we showed that functionalized hydrogels with grafted arginine-glycine-aspartate (RGD) peptides and lower degree of crosslinking can promote the proliferation of human mesenchymal stem cells (hMSCs) and upregulate the expression of cell receptor proteins. Moreover, grafted RGD and histidine-alanine-valine (HAV) peptides in hydrogel scaffolds can regulate the adhesion of the intercellular at an early stage. In the second phase, we confirmed that simultaneous use of HAV and RGD peptides led to greater chondrogenic differentiation compared to the blank control and single-peptide groups. Furthermore, the controlled release of kartogenin (KGN) can better facilitate cell chondrogenesis compared to other groups. Interestingly, with longer culture time, cell condensation was clearly observed in the groups with RGD and HAV peptide. In all groups with RGD peptide, significant matrix deposition was observed, accompanied by glycosaminoglycan (GAG) and collagen (Coll) production. Through in vitro and in vivo experiments, this study confirmed that our hydrogel system can sequentially promote the proliferation, adhesion, condensation, chondrogenic differentiation of hMSCs, by mimicking the cell microenvironment during neo-chondrogenesis.
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