Enhanced tenogenic differentiation and tendon-like tissue formation by tenomodulin overexpression in murine mesenchymal stem cells

被引:34
作者
Jiang, Yongkang [1 ]
Shi, Yuan [1 ]
He, Jing [3 ]
Zhang, Zhiyong [1 ,2 ]
Zhou, Guangdong [1 ,2 ]
Zhang, Wenjie [1 ,2 ]
Cao, Yilin [1 ,2 ]
Liu, Wei [1 ,2 ]
机构
[1] Shanghai 9th Peoples Hosp, Dept Plast & Reconstruct Surg, Shanghai, Peoples R China
[2] Natl Tissue Engn Ctr China, Shanghai, Peoples R China
[3] Tongji Univ, Sch Med, Dept Anat & Neurobiol, Shanghai, Peoples R China
关键词
tenomodulin; overexpression; MSCs; tenogenic differentiation; neotendon formation; MARROW STROMAL CELLS; CHONDROMODULIN-I; ENGINEERED TENDON; MOLECULAR-CLONING; COLLAGEN FIBRILS; PROGENITOR CELLS; DEFICIENT MICE; SCLERAXIS; REPAIR; GENE;
D O I
10.1002/term.2150
中图分类号
Q813 [细胞工程];
学科分类号
摘要
As a highly specific marker of tenocytes, tenomodulin (Tnmd) functions remain largely unexplored. We investigated the effect of Tnmd overexpression on tenogenic differentiation of murine mesenchymal stem cells (mMSCs) via plasmid-mediated overexpression in the C3H10T1/2 cell line. The results showed that overexpressed Tnmd could significantly enhance cell proliferation (p<0.05) and the gene expressions of tenogenic-related molecules, including Tnmd, Scleraxis (Scx), collagens I, III and VI and decorin (p<0.05), and significantly inhibit mMSCs differentiation towards the adipogenic, chondrogenic and osteogenic lineages (p<0.05). Upon in vivo implantation with rat tail collagen gel subcutaneously in nude mice, Tnmd-overexpressed C3H10T1/2 cells formed neotendon-like tissue, which revealed a histological feature of wave-like dense collagen fibres and cells aligned in parallel. By contrast, a disorganized connective tissue structure with randomly distributed cells was observed in the control group. To further confirm this finding, a conditional Tnmd-overexpressing mouse model was established and the derived primary mMSCs could be induced to overexpress Tnmd with>two-fold upregulated gene expression (p<0.05) by the treatment of doxycycline (Dox). Similarly, conditional overexpression of Tnmd in primary mMSCs also led to faster proliferation (p<0.05), enhanced gene expression of tenogenic markers (p<0.05) and the inhibited expressions of adipogenic and osteogenic markers (p<0.05). The results of enhanced tenogenic differentiation and neotendon formation indicated that Tnmd may serve not only as a tenogenic marker but also as a positive regulator of MSCs tenogenic differentiation, which might be applied to MSCs-mediated tendon regeneration. Copyright (C) 2016 John Wiley & Sons, Ltd.
引用
收藏
页码:2525 / 2536
页数:12
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