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
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