Enhanced chondrogenic differentiation of human mesenchymal stems cells on citric acid-modified chitosan hydrogel for tracheal cartilage regeneration applications

被引:48
|
作者
Chen, Hao [1 ]
Wang, Hao [1 ]
Li, Biyun [2 ]
Feng, Bei [1 ,3 ]
He, Xiaomin [1 ,3 ]
Fu, Wei [1 ,3 ]
Yuan, Huihua [2 ]
Xu, Zhiwei [1 ,3 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Shanghai Childrens Med Ctr, Dept Pediat Cardiothorac Surg, Shanghai 200127, Peoples R China
[2] Nantong Univ, Sch Life Sci, Nantong 226019, Jiangsu, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Med, Shanghai Childrens Med Ctr, Inst Pediat Translat Med, 1678 Dong Fang Rd, Shanghai 200127, Peoples R China
来源
RSC ADVANCES | 2018年 / 8卷 / 30期
基金
中国国家自然科学基金;
关键词
CROSS-LINKED CHITOSAN; IN-VITRO; TISSUE; SCAFFOLDS;
D O I
10.1039/c8ra00808f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Congenital tracheal stenosis in infants and children is a worldwide clinical problem. Tissue engineering is a promising method for correcting long segmental tracheal defects. Nonetheless, the lack of desirable scaffolds always limits the development and applications of tissue engineering in clinical practice. In this study, a citric-acid-functionalized chitosan (CC) hydrogel was fabricated by a freeze-thaw method. Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) confirmed that citric acid was successfully attached to the chitosan hydrogel. Scanning electron microscopy (SEM) images and compression tests showed that the CC hydrogel had an interconnected porous structure and better wet mechanical properties. Using morphological and proliferation analyses, cell biocompatibility of the CC hydrogel was shown by culturing human mesenchymal stem cells (hMSCs) on it. Specific expression of cartilage-related markers was analyzed by real-time polymerase chain reaction and western blotting. The expression of chondrocytic markers was strongly upregulated in the culture on the CC hydrogel. Hematoxylin and eosin staining revealed that the cells had the characteristic shape of chondrocytes and clustered into the CC hydrogel. Both Alcian blue staining and a sulfated glycosaminoglycan (sGAG) assay indicated that the CC hydrogel promoted the expression of glycosaminoglycans (GAGs). In a nutshell, these results suggested that the CC hydrogel enhanced chondrogenic differentiation of hMSCs. Thus, the newly developed CC hydrogel may be a promising tissue-engineered scaffold for tracheal cartilage regeneration.
引用
收藏
页码:16910 / 16917
页数:8
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