Recruitment of exogenous mesenchymal stem cells in mandibular distraction osteogenesis by the stromal cell-derived factor-1/chemokine receptor-4 pathway in rats

被引:37
作者
Cao, Jian [1 ,2 ]
Wang, Lei [1 ]
Du, Zhao-jie [1 ]
Liu, Peng [1 ]
Zhang, Ya-bo [1 ]
Sui, Jian-fu [1 ]
Liu, Yan-pu [1 ]
Lei, De-lin [1 ]
机构
[1] Fourth Mil Med Univ, Sch Stomatol, Dept Oral & Maxillofacial Surg, Xian 710032, Peoples R China
[2] Mil Gen Hosp Lanzhou Command, Dept Oral & Maxillofacial Surg, Lanzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Distraction osteogenesis; Mesenchymal stem cells; Homing; Stromal cell-derived factor-1; CXC chemokine receptor 4; BONE-MARROW; MYOCARDIAL-INFARCTION; PROMOTING MIGRATION; INJURY; CXCR4; MECHANISMS; FRACTURE; STRESS; BLOOD; MICE;
D O I
10.1016/j.bjoms.2013.05.003
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Distraction osteogenesis is widely used in orthopaedic and craniofacial surgery. However, its exact mechanism is still poorly understood. The purpose of this study was to find out whether there is systemic recruitment of mesenchymal stem cells (MSC) to the neocallus in the distraction gap by the stromal cell-derived factor-1 (SDF-1)/CXC chemokine receptor 4 (CXCR4) axis during osteogenesis. We examined the migration of MSC towards a gradient of SDF-1 in vitro. We also transplanted MSC labelled with green fluorescent protein (GFP) intravenously, with or without treatment with CXCR4-blocking antibody, into rats that had had unilateral mandibular distraction osteogenesis, and investigated the distribution of cells labelled with GFP in the soft callus after 24 h. We found that SDF-1 facilitated the migration potency of MSC both in vitro and in vivo, and this migration could be inhibited by AMD3100, an antagonist of CXCR4, and promoted by local infusion of exogenous SDF-1 into the distraction gap. This study provides a new insight into the molecular basis of how new bone is regenerated during distraction osteogenesis. (C) 2013 The British Association of Oral and Maxillofacial Surgeons. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:937 / 941
页数:5
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