软骨发生
细胞外基质
阿格里坎
软骨
化学
间充质干细胞
细胞生物学
II型胶原
软骨寡聚基质蛋白
再生(生物学)
基质(化学分析)
组织工程
蛋白多糖
解剖
生物医学工程
病理
生物
骨关节炎
医学
关节软骨
替代医学
色谱法
作者
Cheng Tang,Chengzhe Jin,Yan Xu,Bo Wei,Liming Wang
出处
期刊:Tissue Engineering Part A
[Mary Ann Liebert, Inc.]
日期:2015-11-25
卷期号:22 (3-4): 222-232
被引量:33
标识
DOI:10.1089/ten.tea.2014.0491
摘要
We previously found that the combination of an autologous bone mesenchymal stem cell-derived extracellular matrix (aBMSC-dECM) scaffold with bone marrow stimulation could enhance hyaline cartilage regeneration. We suspected that chondrogenic differentiation could be induced by the aBMSC-dECM scaffold. This study aimed to investigate whether aBMSC-dECM scaffolds could promote chondrogenic differentiation without exogenous growth factors. BMSCs were seeded on aBMSC-dECM scaffolds and cultured in vitro with or without transforming growth factor-β3 (E+ or E− group). Atelocollagen scaffolds were used as controls (C+ or C− group). The chondrogenic differentiation was evaluated by histological, biochemical, and real-time polymerase chain reaction assays. After 3 weeks, cartilage-like tissue with a homogeneous structure, a high cartilaginous matrix content (proteoglycan and type II collagen), and high expression levels of cartilage-associated genes (COL2A1, ACAN, and SOX9) were observed in the E+, E−, and C+ groups. In addition, BMSCs in each scaffold (E group or C group) were preconditioned with chondrogenic media in vitro for 1 week, and then implanted in the backs of nude mice for 3 weeks. Three weeks later, cartilage matrix formation (proteoglycan and type II collagen) was achieved only in the E group, confirmed by safranin O staining and immunohistochemical staining for type II collagen. Taken together, these results indicate that aBMSC-dECM scaffolds could induce chondrogenic differentiation. Thus, they could be successful candidate scaffolds for cartilage tissue engineering.
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