共 50 条
Osteogenic differentiation of human umbilical cordderived mesenchymal stem cells promoted byoverexpression of osterix
被引:1
|作者:
Huang, Shengyun
[1
]
Jia, Shanshan
[2
]
Liu, Guijun
[1
]
Fang, Dong
[3
]
Zhang, Dongsheng
[1
]
机构:
[1] Shandong Univ, Prov Hosp, Dept Oral & Maxillofacial Surg, Jinan 250021, Shandong, Peoples R China
[2] Shandong Univ, Prov Hosp, Dept Orthodont, Jinan 250021, Shandong, Peoples R China
[3] Shandong Univ, Prov Hosp, Dept Oral Radiol, Jinan 250021, Shandong, Peoples R China
关键词:
Osteogenic differentiation;
osterix;
umbilical cord-derived mesenchymal stem cells;
TRANSCRIPTION FACTOR OSTERIX;
HUMAN BONE-MARROW;
OSTEOBLAST DIFFERENTIATION;
IN-VITRO;
PROLIFERATION;
OSTEOPONTIN;
CORD;
MINERALIZATION;
EXPRESSION;
SURVIVAL;
D O I:
10.5372/1905-7415.0706.236
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
Background: Umbilical cord-derived mesenchymal stem cells (UC-MSCs) are considered to be multipotent mesenchymal stem cells that are easily induced to differentiate into functional osteoblasts both in vitro and in vivo. Osterix (Osx), a novel zinc-finger-containing transcription factor of the Sp family, is required for osteoblast differentiation and bone formation. Objective: We investigated the effect of Osx on the proliferation and osteogenic differentiation of the UC-MSCs. Method: The primary UC-MSCs were isolated and cultured. An Osx-expressing plasmid (pEGFP-Osx) was constructed and transfected into UC-MSCs. Then expression of bone morphogenesis-related genes, proliferation rate, alkaline phosphatase activity, and mineralization were examined to evaluate the osteogenic potential of the Osx gene-modified UC-MSCs. Result: UC-MSCs transfected with pEGFP-Osx exhibited apparent osteogenic differentiation as determined by increased activity of alkaline phosphatase, the formation of mineralized nodules and the expression of related osteoblastic genes. Conclusion: These results confirmed the ability of Osx to enhance osteoblast differentiation of UC-MSCs in vitro, and the Osx gene-modified UC-MSCs are potential as novel cell resources of bone tissue engineering.
引用
收藏
页码:743 / 752
页数:10
相关论文