共 41 条
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
相关论文