Osteogenic potential of mesenchymal stem cells from rat mandible to regenerate critical sized calvarial defect

被引:34
作者
Lee, Dong Joon [1 ,2 ]
Kwon, Jane [1 ,2 ]
Current, Luke [1 ,2 ]
Yoon, Kun [1 ,2 ]
Zalal, Rahim [1 ,2 ]
Hu, Xiangxiang [1 ,2 ]
Xue, Peng [1 ,2 ]
Ko, Ching-Chang [1 ,2 ,3 ]
机构
[1] Univ N Carolina, Oral & Craniofacial Hlth Sci Res, Sch Dent, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, North Carolina Oral Hlth Inst, Sch Dent, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Orthodont, Sch Dent, 275 Brauer Hall,Campus Box 7454, Chapel Hill, NC 27599 USA
关键词
Mesenchymal stem cells from mandible; critical sized defect; mandible; craniofacial bone tissue engineering; DIFFERENTIATION; DENTISTRY; PROMOTES;
D O I
10.1177/2041731419830427
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Although bone marrow-derived mesenchymal stem cells (MSCs) have been extensively explored in bone tissue engineering, only few studies using mesenchymal stem cells from mandible (M-MSCs) have been reported. However, mesenchymal stem cells from mandible have the potential to be as effective as femur-derived mesenchymal stem cells (F-MSCs) in regenerating bone, especially in the orofacial regions, which share embryonic origin, proximity, and accessibility. M-MSCs were isolated and characterized using mesenchymal stem cell-specific markers, colony forming assay, and multi-potential differentiation. In vitro osteogenic potential, including proliferation, osteogenic gene expression, alkaline phosphatase activity, and mineralization, was examined and compared. Furthermore, in vivo bone formations of F-MSCs and M-MSCs in rat critical sized defect were evaluated using microCT and histology. M-MSCs from rat could be successfully isolated and expanded while preserving their MSC's characteristics. M-MSCs demonstrated a comparable proliferation and mineralization potentials and in vivo bone formation as F-MSCs. M-MSCs is a promising cell source candidate for craniofacial bone tissue engineering.
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页数:13
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